WO1997004133A1 - Analysis of alpha integrins for the diagnosis of diabetic nephropathy - Google Patents

Abstract

Analysis of alterations in integrin subunit expression, particularly α1 and/or α2 integrin subunit expression from integrin producing cells as compared to normal controls as a diagnostic method to identify individuals who have or are predisposed to pathologies associated with altered matrix deposition, such as diabetic renal nephropathy.

Description

ANALYSIS OF ALPHA INTEGRINS FOR THE DIAGNOSIS OF DIABETIC NEPHROPATHY

Background of the Invention Diabetic nephropathy is a major cause of renal failure in the U.S. and develops in approximately 30% of insulin dependent diabetes mellitus (IDDM) patients. Recent studies by the Diabetes Control and Complications Trial Group have indicated that intensive insulin treatment substantially reduces the risk of developing complications, including nephropathy. However, the cost and effort ofthe intensive therapy, as well as the danger of hypoglycemic attacks dictate that this treatment should be limited to those patients who are prone to develop complications. It follows that an early selection of these diabetic subjects would be extremely helpful, but currently there are no adequate predictors available for clinical use.

Metabolic imbalance caused by hyperglycemia has been implicated as a major factor in the development of this condition and is associated with a genetic tendency to develop nephropathy. A prominent expansion ofthe mesangium with changes in the composition ofthe mesangial matrix have been observed in diabetic nephropathy (Williamson et al., Diabetes Met. Rev. 4:339 (1988), Steffes, M.W., et al. Diabetes 38:1077-81 (1989)). Studies performed with human and experimental animal mesangial cells cultured in high-glucose medium have demonstrated an increased synthesis and accumulation of matrix proteins, namely collagens, including collagen type IV and fibronectin. This suggests that hyperglycemia plays a role in the mesangial changes of diabetic nephropathy. Ayo, S.H., et al. (1990a), Am. J. Pathol. 136:1339-1348; Nahman, N.S., et al., Kidney Int. 41 :396-402 (1992); Danne, T., et al, Diabetes 42:170-177 (1993).

The changes in the matrix secretion pattern ofthe cell are mediated either directly by hyperglycemia or by the glycation of mesangial matrix on prolonged exposure to high levels of glucose. Studies have demonstrated that cultured mesangial cells are influenced by the glycation of matrix leading to altered cell adhesion, spreading and proliferation. Since collagen IV (cIV) is the major component ofthe mesangial matrix

(about 60%), changes in the interactions between this major mesangial glycoprotein and mesangial cells may play an important role in the pathology of diabetic nephropathy. Kim, Y., et al., Am. J. Pathol. 138:413-420 (1991). The changes in matrix deposition are secondary in time to insulin insufficiency. Altered matrix deposition including basement membrane thickening is also found in a variety of arterioles and arteries in patients with diabetes mellitus. Altered matrix deposition is found in the pancreas of diabetic patients. Altered matrix deposition puts diabetic patients at risk for developing secondary pathological changes including, but not limited to nephropathy, myocardial infarction, cerebral stroke, problems associated with reduced circulation, retinopathy, neuropathies and the like.

Cell-matrix interactions are mediated, for the most part, by a family of receptors known as integrins. The very late antigen (VLA) subgroup of integrins which share a common β 1 chain, include the cell membrane receptors for cl V, α 1 β 1 and α2β 1.

Although integrins are mainly studied for their role in cell differentiation, migration and signaling events, they may also be involved in the maintenance of tissue structure. For instance, cells can modify their matrix by altering the production of matrix proteins and/or by regulating matrix organization. Cells cultured under high glucose conditions resulted in an increased production of matrix components by mesangial cells.

(Kashgarian, M., et al., Kidney Int. 41:524-529 (1992).) The balance of cell surface integrin expression has been demonstrated to be altered in various disease states including inflammation and malignancy (Waes and Carey, Otolarnyngologic Clinics of North America 25(5): 1117 (1992); Adams, J.C, et al., Cell 63:425-435 (1990); Rozzo et al., FEBS Letters 332:263 (1993)). This altered expression has been associated with altered adhesion to extracellular components.

Presently, the only earliest available indicator of kidney changes is microalbuminuria which occurs after the appearance of nephropathic changes. Yet only a percentage of individuals with microalbuminuria go on to develop glomerulopathy. Individuals at risk for developing glomerulopathy are best treated with intense glucose- modulating therapies that have their own risk. Often physicians are hesitant to place individuals with microalbuminuria on such therapies since the majority of these patients do not proceed to glomerulopathy. Biopsies indicating the accumulation of matrix accompanying the expansion ofthe mesangium occur at a point when the process has become irreversible. Therefore an early predictor of nephropathy or other disease states associated with altered matrix deposition would be beneficial as an indicator of those patients who require stringent control of blood glucose levels to minimize nephropathic and other altered matrix deposition-associated disorders.

Thus, there is a need to identify markers associated with the changes seen in nephropathy and in other altered matrix deposition-associated disorders for the diagnosis of these disorders. There is a need to identify changes in regulation and function of integrins in diabetic patients and there is a need to develop a diagnostic test that can be used to identify patients who are likely to develop or have the early symptoms of nephropathy.

Summary of he Invention

Alterations in the amounts and patterns of alpha-integrin subunits has now been correlated to the onset of nephropathy. Analysis of alpha integrin subunit expression as compared with controls provides a diagnostic tool for the determination of patients likely to develop severe nephropathy and a method to monitor progress of disease during treatment protocols.

Cells that express alpha integrins, such as kidney tissue, fibroblasts, endothelial cells, and blood cells are analyzed for alpha integrin subunit expression, for example, by in situ hybridization methods. Changes in the amounts and pattern of integrin subunit expression as compared with control samples, is diagnostic of nephropathy and can be used to screen individuals, e.g., diabetic patients at risk for developing severe disease.

Analysis of αl, α2, α3, α5, and beta-1 integrin subunit expression as compared with control tissue expression is preferred. An increase in α2, α3, α5, or beta-1 integrin expression and/or a decrease in αl expression is diagnostic of increased risk of nephropathy. An especially preferred diagnostic method is the comparison of αl and α2 integrin subunit expression with control tissue. A pattern change including a decrease in αl and an increase in α2 is diagnostic of increased risk of nephropathy or onset ofthe disease.

Brief Description of the Drawings Figure 1 is a histogram summarizing results of In situ hybridization studies of rat control and diabetic tissue with αl and α2 integrin probes. Detailed Description of the Invention

Analysis of changes in the pattern of integrin subunit expression, particularly of alpha integrin subunits, is made by comparing expression in sample tissues as compared with tissue controls.

Tissue Samples:

The invention is directed to methods of detecting changes in α integrin subunit expression in cells, such as the cell populations (visceral epithelial, endothelial and mesangial and other matrix-producing cells) present in the glomerulus; and also in the tubules as well as including, but not limited to, fibroblasts (for example see D. Kyu Jin, et al. inJ. Am. Society ofNephrology, 5(3): 966, 1994), epithelial, and endothelial cells from a variety of tissues and organs as well as blood cells including, but not limited to polymorphonuclear leukocytes, monocytes, and the like. Changes to blood cells, including leukocytes, have been reported in diabetic patients who develop nephropathy (Ng, et al. Diabetologia 33 :278-284, 1990).

A change in the expression of αl and α2 integrins has been detected in the studies disclosed here, under conditions ofhigh glucose (i.e., about 25 mM) compared with low glucose (i.e., about 5 mM), in diabetic test animals in vitro, and in a human diabetic patient with neuropathy. Mesangial cells cultured in high glucose showed an increase in α2 integrin expression and a decrease in αl integrin expression compared with mesangial cells grown under low glucose conditions. A change in expression of α integrins such as αl and/or α2 subunits can be used to identify patients that have or will develop diabetic nephropathy. In view of these studies, it is believed that patients showing about a 25 to 100% decrease in αl integrin and/or about a 25 to 100% increase in α2 integrin expression have a greater chance of developing diabetic nephropathy.

The methods disclosed here are useful to identify diabetic patients at risk for developing diabetic nephropathy. The methods may also be useful to monitor progression of diabetic nephropathy. Patients identified as having a risk for developing or showing early symptoms of diabetic nephropathy can be placed on a strict glucose control regimen so that the development and/or progression of nephropathy can be inhibited. Changes in integrin subunit expression in diabetic patients have been identified in cultured human skin fibroblasts taken from skin biopsies (D. Kyu Jin, et al., J. Am. Soc. ofNephrology 5(3):966, 1994) suggesting that a variety of integrin-expressing cells could be momtored to identify individuals with a predisposition to nephropathy or to other complications associated with diabetes-induced altered matrix deposition.

Methods of Detecting a Change in Expression of αl and/or α2 Integrin Subunits in

Cells from Diabetic Patients

The methods ofthe invention are conducted with cell types that express alpha

(α) integrin subunits. Preferably, to identify patients predisposed to nephropathy, the cells are obtained from tissue samples from biopsy of kidney tissue of diabetic patients. However, other cell types that express α integrin subunits can be utilized including, but not limited to, fibroblasts, endothelial cells, polymoφhonuclear leukocytes, monocytes, and other blood cells. The amount of cells typically obtained is relatively small so that the detection methods selected are those that can detect and/or quantitate α integrin subunit expression in a small cell sample. These methods include, but are not limited to in situ hybridization, including polymerase chain reaction (PCR) enhanced in situ hybridization (also known as in situ PCR) and the like.

The cell samples are obtained from patients having diabetes but having no demonstrable symptoms or signs of nephropathy. The earliest change in nephropathy is the detection of microalbuminuria. Biopsy specimens may also be obtained from diabetic patients that may have early symptoms of nephropathy so that the progression of diabetic nephropathy can be monitored. Blood samples and skin biopsies also can be obtained from patients with diabetes and processed for either in situ hybridization or PCR enhanced in situ hybridization (also known as in situ PCR). Similarly, it is possible to perform in situ hybridization or PCR enhanced in situ hybridization using a cheek scraping or a scraping of other accessible tissue.

Biopsy tissue samples are usually about 1mm and are obtained using standard biopsy methods. Where the kidney is the organ selected for biopsy, kidney tissue from the cortical region is preferred although biopsy samples can be obtained elsewhere. Fibroblasts can be obtained from skin or any other tissue. The biopsy samples are then frozen in liquid nitrogen or fixed in 4% fresh paraformaldehyde and sectioned into 5 μm thick sections on silane-coated slides. The sections can then be treated with reagents to detect and/or quantitate α integrin expression in cells. Blood cells and other α integrin expressing cells can also be analyzed for changes in α integrin subunit expression. These cells include fibroblasts, monocytes, polymorphonuclear leukocytes and other blood cells. Cells can be obtained and isolated from a blood or bone marrow sample. Methods for isolating particular cell types from a blood sample are well known in the art. Preferably leukocytes are isolated from blood by centrifugation, followed by hypotonic shock of residual blood cells as disclosed by Ng, et al. Diabetologia 33:278-284, 1990.

Rather than preparing cell sections, the sample of cells can be extracted to obtain nucleic acids using standard methods. The nucleic acids encoding αl and/or α2 integrin subunits can be amplified using any of a variety of polymerase chain reaction methods.

For example, changes in the level of expression of αl and/or α2 integrins can be detected using a competitive PCR method as described by Gilland, G., Proc. Natl. Acad. Sci. (USA) 87:2725 (1990).

In a method ofthe invention, the level of αl integrin expression is detected and/or quantitated in cells such as glomerular and tubular kidney cells. The level of α 1 integrin expression can be detected using a variety of standard methods. The preferred methods are in situ hybridization, in situ PCR for detection of integrin RNA and immunofluorescence detection of antibody-tagged integrin protein. A decrease of about 25 to 100% in αl integrin expression can indicate that early changes of diabetic nephropathy are occurring and can be used to identify patients that have an increased risk of developing diabetic nephropathy. A decrease in αl integrin expression is compared to the level of αl integrin expression in cells from age matched non-diabetic controls.

For detection and quantitation using in situ hybridization, the following method is preferred: a detectably labeled probe that is complementary to and/or hybridizes to all or a portion of nucleic acid sequences encoding all or a portion of αl integrin subunit is utilized. A radioactively labeled probe preferably has a specific activity of about 2x10 to lxl 0⁹ dpm/μg. In situ hybridization on cells such as kidney tissue can be conducted as follows. 5μm tissue sections, fibroblasts and/or blood cells on silane-coated slides are further fixed in fresh 4% paraformaldehyde for 10 min. The slides are then pretreated with 0.2N HCl for 20 min., 0.05 M Triethanolamine (TEA, Sigma) for 15 min, 0.005% digitonin for 5 min., 3 μg/ml proteinase K (Sigma) for 15 min. at 37°C, and 0.3% acetic anhydride - O.IM TEA for 10 min. Hybridization is performed at 50°C overnight in 50% formamide, 0.6 M NaCl, lxDenhardt's, 0.17 μg/ml human COT^RT DNA (GIBCO/BRL), 1 mg/ml poly A (Boehringer Mannheim), 10% (W/V) Dextran sulfate (Sigma), 0.1 M dithiothreitol (DTT, Boehringer Mannheim), 1 mM EDTA, 0.1 mM aurinitricarboxylic acid (ATA, Sigma) and S³⁵-dCTP labeled cDNA probe. The following day, the slides are washed in 2x SCC-0.05% SDS for 60 min. at 55°C; further washed in the high stringency washing buffer containing 50% formamide, 0.6 M NaCl, 1 mM EDTA, 5 mM DTT and 10 mM Hepes for 4 days at room temperature. After 4 days, the slides are rinsed in 2x SCC and the slides are dehydrated in graded ethanol with 0.3 M ammonium acetate, then dipped in Kodak NTB-2 emulsion and exposed for 5 days at 4°C. After development, the slides are stained with hematoxylin-eosin (Surgipath Canada, Inc., Winnipeg, Canada) and mounted. The silver grain number per cell are used to quantitate the result of in situ hybridization. About 10-20 glomeruli and a similar number of tubules are examined per patient. A probe ofthe invention hybridizes to and is complementary to and/or all or a portion of a nucleic acid sequence encoding αl integrin as long as the probe specifically detects αl integrin expression. Probes can be designed using a known sequence such as the rat αl integrin sequence as shown as Figure 2 in Takada and Hemnlev, J. Cell Biol. 109:397-407 (1983) or by the use of commercially available programs and are capable of binding to rodent or human αl integrin but are not capable of binding to other proteins including other proteins having regions homologous to α integrins when tested under identical hybridization conditions. Examples of other proteins that have homologous regions to α integrins include those proteins identified using a gene bank search, such as GenBank, or the like, or in publications related to αl and α2 subunits (for example, see Ignatius, et al. J. Cell Biol. 111 :709-720, 1990 listing proteins with homologies to the αl -subunit).

The probe can be about 15 nucleotides long up to a full length probe of about 4kb. The probes are preferably 100% complementary to the nucleic acid encoding αl integrin however some mismatches can be present depending on the length ofthe probe. About 1 to 3 mismatches in a probe of about 20 to 30 nucleotides long can be present a long as hybridization conditions are adjusted to account for mismatches. Hybridization conditions can be adjusted to take into account mismatches in accord with known principles as described in Sambrook et al., A Guide to Molecular Cloning. Cold Spring Harbor NY (1989).

A specific example of a nucleic acid sequence encoding αl integrin is the rat αl integrin sequence shown as Figure 2 in Ignatius et al., J Cell. Biol. 111 :709-720, 1990, (SEQ ID NO: 1) and the protein sequence encoded by αl integrin is provided as SEQ ID

NO:2. A DNA sequence encoding αl integrin can be obtained from a rat pheochromocytoma cell line PC 12 as described by Ignatius et al., J Cell. Biol. I l l :709 (1990). Briefly, a cDNA library can be prepared from rat pheochromocytoma PC 12 in a lambda vector. The sequence can be identified and/or amplified using probes or primers designed from the known sequences using standard methods as described in Sambrook et al., (supra). Once the sequence is subcloned it can be confirmed by sequence analysis and/or by screening with antibodies specific for αl integrin. Other DNA sequences encoding αl integrins can be identified and isolated using probes and primers derived from the known sequences. A preferred probe is a 3.9 kb fragment from the 5' end through the EcoRI site near base 3900 including the sequence as shown in Figure 2 of Ignatius et al. (supra). Smaller fragments that can form probes can readily be prepared with restriction enzymes or derived by automated or manual oligonucleotide synthesis techniques, by PCR, or by other methods also known in the art. The probes are preferably detectably labeled with a radioactive nucleotide using standard methods.

Other methods utilizing probes for detection of αl integrin expression can also be utilized using standard methods such as Northern Blot Analysis and the like as described in Sambrook et al., cited supra.

Primers can also be designed based upon the sequence of rat αl integrin sequence. This invention also contemplates using primers and nucleic acid sequences from the human αl integrin sequence provided by Briesewitz, et al. (J. Biol. Chem. 268(4):2989-96, 1993). Primers can be designed using a known sequence using commercially available computer programs. Primers typically are complementary to and/or hybridize to a 5' region and/or a 3' region ofthe nucleic acid sequence encoding the protein of interest. The primers can be used to amplify all or a portion of DNA or cDNA encoding αl integrin. Primers can be used to make probes and to detect expression levels of αl integrin. Primers preferably have at least 15 nucleotides that are 100% complementary to the nucleotide sequence selected. The primers can also have additional sequences preferably at the ends ofthe primer that include restriction enzyme sites and the like that are not complementary to the nucleic acid sequence to be amplified. Primers are preferably about 15 to 50 nucleotides long and can be prepared by automated synthesis.

The primers can be used to detect the level of αl expression in cells. RNA from cells is extracted and reverse transcribed using standard methods. Primers mat are complementary to and can hybridize to a DNA sequence encoding αl integrins are utilized to amplify the cDNA. A decrease in the level of PCR product can be determined in comparison to the amount of PCR product obtained from control cells. One method of utilizing PCR to detect αl integrin expression is in situ PCR. A method for PCR in situ hybridization is described in PCR In Situ Hybridization Protocols and Applications. J. Novo ed., "PCR In Situ Hybridization", pp. 157-183. Briefly, tissue sections, fibroblasts and/or blood cells (about 5 μm) are placed on silane- coated glass slides. After removing paraffin, the slides are treated with trypsinogen

(2mg/ml) in 0.0 IN HCl for 10 minutes and then trypsinogen inactivated in 0.1M Tris HCl (pH 7.0) solution. The slides are washed sequentially in 90% and 100% ethanol, two times for 1 minute each and air dried. Aliquots of reaction mixture containing 0.15 units/ml Taq DNA polymerase and specific primer pairs for αl integrin are added to the tissue section and then overlaid with siliconized glass coverslips. The slides are placed in the heat-sealable plastic bags and 4-5ml mineral oil is added. After removing air, the bag is heat-sealed and placed in the thermal-cycling oven for 40 cycles. After thermal- cycling, the slides are washed twice in chloroform for 2 minutes. The coverslips are removed and the slides are dipped briefly in fresh chloroform. After washing in PBS fo 5 minutes, the slides are dehydrated and air-dried. The slides are dipped in NTB2 nuclear emulsion (Kodak) and exposed in the dark for 7 days. After development, the slides are counterstained with hematoxylin-eosin.

A change in the level of αl integrin protein expression can also be detected by using immunofluorescence. (Unless otherwise specified as "protein expression", the term "expression" used herein generally refers to RNA expression.) Sections of tissue samples, fibroblasts and/or blood cells can be stained with antibodies specific for αl integrin. It is preferable that antibodies are monoclonal antibodies and are antibodies that do not substantially cross-react with other α integrin subunits. Antibodies to αl integrin can be made by standard methods such as described in Wayner EA and WG Carter, 1987, J. Cell Biol. 121(5):1141-1152. Antibodies specific to αl integrin include the SR84 and TS2/7 antibodies. Information related to these antibodies is provided in Examples 1 and 3. A decrease in the level of immunofluorescence can be observed and quantitated using standard methods. A decrease of about 25 to 100% of αl integrin expression may be used to identify patients that have a greater risk of developing diabetic nephropathy. A decrease in αl integrin expression is compared to the level of αl integrin expression in age-matched nondiabetic controls. The preferred method ofthe invention involves comparing the level of expression of α2 integrin to the level of expression of αl integrin. Under high glucose conditions, a decrease in the level of αl expression is seen as well as an increase in the level of α2 expression in mesangial cells. It is believed that patients at greater risk for nephropathy or other complications associated with diabetes will exhibit an increase in α2 expression and a decrease in αl expression. A change of about 15 to 100%, and preferably of about 25 to 100%, of α2 integrin expression as well as a change of about 15 to 100%, and preferably of about 25 to 100%, of αl integrin expression is believed to be indicative of patients with a greater risk of developing diabetic nephropathy. Integrin expression is associated with a variety of cell types in a variety of locations throughout the body, therefore it is possible that altered levels of integrin expression will also be identified in diabetic associated retinopathy, atherosclerosis and select diabetic neuropathies.

The expression of integrin subunits, preferably of αl and α2 integrin subunits, is detected and/or quantitated in tissue samples, fibroblasts and/or blood cells from diabetic patients. The preferred methods are those that allow detection of gene expression in a small amount of cells or tissue.

The expression of α2 integrin can be detected using in situ hybridization. The conditions for in situ hybridization are the same as those described previously. A probe specific for nucleic acid sequences encoding α2 integrin can be prepared using standard methods as described in Sambrook et al., cited supra. The probes are complementary to and/or hybridize to all or a portion of a nucleic acid sequence encoding α2 integrin. As described for αl integrin, the probe to detect α2 integrin can hybridize to a portion of a nucleic acid sequence as long as the probe specifically detects a sequence encoding α2 integrin. Nucleic acid sequences can be DNA, cDNA, or RNA. It is preferred that the probe hybridize to RNA or cDNA.

A specific example of nucleic acid sequence encoding α2 integrin is shown in Figure 2 of Takada and Hemler, J. Cell Biol. 109:397 ( 1989). (SEQ ID NO:3). DNA sequence encoding human α2 integrin can be isolated as described in this reference. The protein encoded by SEQ ID NO:3 is provided in this disclosure as SEQ ID NO:4. Nucleic acid sequences encoding α2 integrin can be obtained from human lung fibroblasts and/or human endothelial cells. Preferably DNA libraries from endothelial cells can be prepared and nucleic acids encoding α2 integrin identified and/or amplified using probes and primers derived from the sequence of α2 integrin, &g., as shown in Figure 2 of Takada et al. (supra). If primers are selected, DNA sequences can be amplified using the polymerase chain reaction and then subcloned. Clones that are positive by hybridization to a probe specific for DNA sequences encoding α2 integrin (see Examples 1 and 3) or that express proteins that are positive by reacting with an antibody specific to α2 integrin such as P1H5 are selected. A DNA sequence encoding α2 integrin can be confirmed by DNA sequencing in comparison to the known α2 sequence, as shown in Figure 2 of Takada et al. {supra).

A probe ofthe invention hybridizes to and is complementary to and/or hybridizes to all or a portion of a nucleic acid sequence encoding α2 integrin as long as the probe specifically detects α2 integrin expression. Probes can be designed using a known sequence such as shown in Figure 2 of Takada et al. (supra) by the use of commercially available programs.

The probe can be about 15 nucleotides long up to a full length probe of about 5Kb. The probes are preferably 100% complementary to the nucleic acid encoding α2 integrin however some mismatches can be present depending on the length ofthe probe. About 1 to 3 mismatches in a probe of about 20 to 30 nucleotides long can be present as long as hybridization conditions are adjusted to account for mismatches. Hybridization conditions can be adjusted to take into account mismatches in accord with known principles are described in Sambrook et al., A Guide to Molecular Cloning. Cold Spring

Harbor NY (1989). A preferred probe is a 1.8 fragment kb from the 5' end through the EcoRI site near base 1800 ofthe sequence shown in Figure 2 of Takada et al. (supra). Other probes can be derived from this fragment or from the full length sequence by use of restriction enzyme digestion. Probes can also be prepared by automated synthesis or by PCR. Probes are preferably detectably labeled with a radioactive nucleotide using standard methods.

Probes specific for α2 integrin expression can then be utilized in methods of detecting α2 integrin expression in various cell types. The preferred method is by use of in situ hybridization or PCR- « situ hybridization on kidney as well as other tissues. The method utilized for in situ hybridization has been described previously (Takada and Hemler, supra). The method for PCR in situ hybridization has been described for αl integrin. Other methods utilizing probes for detection of α2 integrin expression can also be utilized using standard methods such as Northern Blot Analysis, and the like, as described in Sambrook et al. cited supra. Primers can also be designed based upon the known DNA sequence encoding human α2 integrin. Primers can be designed from a known sequence such as shown in Figure 2 of Takada et al. (supra), using commercially available software. Primers typically are complementary to and/or hybridize to a 5' region and/or a 3' region. The primers can be used to amplify all or a portion of DNA or cDNA encoding α2 integrin. Primers can be used to make probes and to detect expression levels of α2 integrin.

Primers preferably have at least 15 nucleotides that are 100% complementary to the nucleotide sequence selected. The primers can also have additional sequence preferably at the ends ofthe primer that include restriction enzyme recognition sites and the like. Primers are preferably about 15 to 50 nucleotides long and can be prepared by automated synthesis.

Primers can be used to detect the level of α2 integrin expression in cells. Nucleic acids, preferably RNA, from cells from diabetic patients are extracted and reverse transcribed using a standard method. Primers that are complementary to and can hybridize to a cDNA sequence encoding α2 integrin are utilized to amplify the cDNA. An increase in the level of PCR product can be determined in comparison to the amount of PCR product obtained from control cells. A change in the level of α2 integrin protein expression can also be detected by using immunofluorescence. Sections from kidneys and/or other tissues, skin fibroblasts and/or blood cells can be incubated with antibodies specific to α2 integrin. It is preferable that the antibodies are monoclonal antibodies and are antibodies that do not crossreact with other α integrin subunits. Antibodies to α2 integrin can be made by standard methods such as described in Wayner EA and WG Carter, 1987, J Cell Biol. 121(5):1141-1152. Antibodies specific for α2 integrin include P1H5. An increase in the level of immunofluorescence can be observed and quantitated using standard methods such as flow cytometry. An increase of about 25 to 100% of α2 integrin expression can be used to identify patients that have a greater risk of developing diabeti nephropathy. An increase in α2 integrin expression is compared to α2 integrin expression in nondiabetic control cells.

An increase in α2 integrin expression alone can also be used to identify a patient that may have a greater risk of developing diabetic nephropathy. An increase in α2 expression can be determined as described using the methods described above. An increase of about 25 to 100% in α2 integrin expression may indicate a patient who has an increased risk of developing diabetic nephropathy.

Although an increase of α2 integrin expression or a decrease of αl integrin expression alone can be utilized to identify patients at greater risk for developing diabetic nephropathy, a preferred method is to detect changes in both αl and α2 integri expression. It is believed that an increase in α2 integrin expression and a decrease in αl integrin expression identifies patients that are at greater risk of or are showing early symptoms of diabetic nephropathy.

In one step ofthe method, the level of α2 to αl integrin is compared. The level of αl integrin expression can be detected and/or quantitated using the methods described previously. The level of αl and α2 integrin expression can be quantitated on two different cell samples such as two sections ofthe same tissue sample. About 10-20 glomeruli and tubules are examined. On one cell sample containing the same type of cells, α2 integrin expression can be quantitated and on a second cell sample with the same type of cells, αl integrin expression can be quantitated. Alternatively, the level o αl and/or α2 integrin expression can be determined using the same cell sample ifthe agent used to detect αl expression is detectably labeled with a first detectable label and the agent used to detect α2 expression is detectably labeled with a second detectable label. The first detectably labeled agent and the second detectably labeled agent are agents selected that can be detected and/or quantitated in the presence of one another. In a preferred version, kidney tissue sections taken from diabetic patients are fixed in formalin and then treated with HCl and proteinase K. A first probe specific for αl integrin is a 3.9 kb fragment from 5' end through EcoRI site near base 3900 probe including a sequence as shown in Figure 2 of Ignatius et al. {supra). This probe is labeled with ³²P or 35S or other suitable labels known in the art including, but not limited to, fluorescent labels, biotinylated labels, or other radio labels and the like. The probe is incubated with the section as described previously. A second section taken from the same tissue sample is treated in the same manner but incubated with a probe specific for α2 integrin expression. In a preferred embodiment, a probe specific for α2 integrin expression is a 1.8 kb fragment from 5' end through EcoRI site near base 1800 that includes a sequence as shown in Figure 2 of Takada et al. (supra). Both probes are labeled with ³²P or ³⁵S. The probe is incubated with the section overnight at 50°C and then for 4 days at room temperature. The sections are then developed for autoradiography. The number of grains per cell are counted for about 10-20 glomeruli and tubules. The total counts for α2 integrin expression vs. αl integrin expression are compared. An increase of about 40% in α2 integrin and a 30-40% decrease of αl integrin may indicate a patient is at greater risk for developing diabetic nephropathy.

In an alternative version, the level of expression of α2 integrin is compared with the αl expression which can be determined using in situ PCR or competitive reverse transcriptase PCR. Primers specific for αl and α2 integrin expression can be prepared as described previously. For competitive reverse transcriptase PCR, RNA extracted from different cell types obtained from diabetic patients will be reverse transcribed to generate cDNA. The cDNA will be mixed with the various concentrations of competitive template amplified by the PCR method. After degradation of competitive cDNA with restriction enzyme, amplified cDNA will be subjected to electrophoresis in 2% agarose gel, electrotransferred to a nylon membrane, UV cross-linked to the membrane and hybridized with a ³²P-labeled probe. Autoradiographs will be used to quantify the label bound to the cDNA using amount of label bound to samples containing target cDNA alone as compared to samples also containing competitor cDNA to arrive at the target cDNA concentration. For in situ PCR, a method has been described previously. The change in αl and α2 integrin expression can be quantitated by coimting the number of grains per cell in control vs. diabetic cells.

Optionally, for each ofthe detection methods for α integrin subunits, the level of integrin subunit expression can be compared to expression of a control. The control is selected to be a protein expressed at the same levels in both normal and diabetic cells. The control protein is also selected to be one that is expressed at sufficient levels for easy detection and quantitation. The level of expression of αl and α2 integrin expression can each be compared to that ofthe level ofthe control RNA expression in the cells. The level of RNA expression of αl integrin or α2 integrin can be divided by the level of expression ofthe control RNA to normalize the values to the level of control expression in a particular cell sample. The level of expression ofthe control protein is detected and quantitated using the same method as αl or α2 integrin expression. The preferred control protein is a cell surface HLA determinant. Optionally, the levels of α3, α5, or beta-1 integrin subunit expression can be analyzed as described above. The level of α3, α5, or beta-1 integrin expression in cells such as kidney tissue can be detected and quantitated as described for αl and α2 integrin expression including in situ hybridization, in situ PCR, immunofluorescence and the like. Other cell types can be analyzed as described above, including fibroblasts and blood cells. Antibodies specific for α3, α5, and beta-1 can be prepared as described by Wayner et al. cited supra.

A DNA sequence encoding α3 integrin has been described in Takada et al., J Cell Biol. 115:257 (1991). A probe specific for cDNA sequence encoding α3 integrin subunit is a 1.4Kb Sal I fragment containing 5' untranslated and amino terminal coding sequences for α3 subunit of integrin. DNA sequences encoding α3, α5, and beta-1 integrin can be utilized to form primers and probes as described previously.

The level of α3, α5, or beta-1 integrin expression is increased about 15 to 100% compared with cells from age matched nondiabetic controls. It is believed that an increase in α3, α5, or beta-1 integrin subunit expression may also identify patients that have an increased risk of developing diabetic nephropathy or that have early signs of diabetic nephropathy. This invention also relates to methods for detecting alterations in integrin subunit expression, particularly αl and/or α2 integrin subunit expression by obtaining a cell sample from a patient, processing the sample to detect alterations in integrin subuni expression as compared to integrin expression in samples from age matched normal controls, detecting levels of integrin expression and determining if these levels are altered relative to controls.

This method is useful for predicting individuals at risk for developing pathologies associated with altered cell matrix deposition, including but not limited to renal nephropathy. In preferred embodiments of this invention, the tissues used to detect altered αl and/or α2 integrin expression include kidney biopsies, skin biopsies and blood cells including polymorphonuclear cells, monocytes, and other cells expression integrin subunits. Biopsied tissue can be further separated into its cellular components or processed as tissue sections for in situ hybridization techniques, and/or for immunodiagnostic techniques including immunofluorescence and immunoperoxidase staining.

The cellular components ofthe biopsied tissue can be cultured for in vitro studies including Northern procedures, PCR techniques, immunofluorescent techniques and/or in situ hybridization techniques. Alternatively, cells can be separated and analyzed by flow cytometry, immunofluorescence, processed for PCR or for any of a variety of techniques discussed throughout this disclosure.

While blood cell components are preferably separated from the whole blood sample using methods well known in the art. Individual cells are separated, where necessary, using techniques such as those of Ng, et al. (supra), and Baron, et al. Clin. Sci. 37:205-219, 1990. Preferably the samples are tested using in situ hybridization methods. Where the amount of tissue available is fairly small, PCR-enhanced in situ hybridization can be used.

The present invention is also directed to a kit to detect alterations in integrin subunit expression, particularly αl integrin and/or α2 integrin subunit expression in a patient sample. A variety of kits are contemplated to encompass a variety of methods. These kits optionally include reagents to process a tissue or cell sample for the technique employed by that particular kit. By example, a kit for PCR or PCR enhanced in situ hybridization can include reagents to process the cell sample or section and isolate the RNA (for PCR). It will also contain suitable primers to amplify the target sequence and additional probes, if necessary, to detect the desired nucleic acid fragments as well as buffers and reagents for the polymerase chain reaction and the buffers and emulsions required to develop the silver granules, and the like, for in situ hybridization methods. Other kits can alternatively include reagents for immunofluorescence using antibodies to the integrin subunits and/or probes, primers and reagents for modifications of in situ or PCR in situ hybridization methods.

All publications and patent applications in this specification are indicative ofthe level of ordinary skill in the art to which this invention pertains. All publications and patent applications are herein incorporated by reference to the same extent as if each individual publication or patent application was specifically and individually indicated by reference.

It will be apparent to one of ordinary skill in the art that many changes and modifications can be made in the invention without departing from the spirit or scope o the appended claims.

Example 1 Effect of High Glucose on the Synthesis and Cell Surface Expression of Integrin Receptors by Cultured Mesangial Cells

Cell lines and culture conditions

Human mesangial cells (HMC) were isolated from 19-22 week old fetal kidney tissue or adult tissue as previously described (Striker and Striker, J. Lab. Invest. 53(2):122-131, 1985). Cells were cultured at 37°C in an environment of 95% air and

5% C0₂ and in media composed of MEM (Sigma, St. Louis, MO) containing 5 or 25 mM glucose, 20% FBS, 15mM Hepes, penicillin (100 U/ml), streptomycin (lOOmg/ml), and amphotericin (25mg/ml). Cells were cultured in the two different conditions for at least two passages before they were used for experiments. Cells were released from their tissue culture flasks for passaging or for use in experiments, by washing twice wit

1 mM EDTA in HBSS and then treating with 0.05% trypsin and 1 mM EDTA in HBSS for 1 min. Cells between passage 4 and 9 were used in experiments. The cells were grown in T-75 flasks until 75-80% confluent. For the adhesion and immunoprecipitation analyses, cells were metabolically labeled for 18 hours with 0.5 mCi of [ S]-methionine per T-75 flask. [ S]-methionine was obtained from Du Pont/NEN, Boston, MA.

Monoclonal antibodies (Mabs) to integrin receptors

Mabs to the integrin receptors α3 (P3D11), α5 (P3D10) and βl (P5D2) can be produced as previously described (Wayner et al., J. Cell. Biol 121(5): 1141 (1993)) and are available from EA Wayner, Fred Hutchinson Cancer Center, Seattle, WA. The antibodies were characterized by sequential immunoprecipitation with known Mabs directed against these integrin receptors (P1B5, P1D6, P4C10) available from EA Wayner. Other Mabs α2 (P1H5), α4 (P4G9) and β2 (P4H9) were previously described (Wayner et al., cited supra 1993) and are available from EA Wayner, Fred Hutchinson Cancer Center, Seattle, WA. TS2/7 was provided by Dr. Martin Hemler (Dana Farber Cancer Institute, Boston, MA).

SR84 supernatant was used as a function-blocking anti-αl Mab in inhibition experiments. SR84 is available from Dr. D.O. Clegg (Univ. of California, Santa Barbara, CA). (α6) G0H3 was purchased from AMAC Inc., Westbrook, ME. In addition monoclonal antibodies to αl and α2 integrin were obtained from Telios Pharmaceuticals (San Diego, CA). Hybridoma culture supernatant or ascites fluid were used for immunoprecipitation, flow cytometry and inhibition experiments. A Mab directed to a cell surface HLA determinant was used as a negative control (W6/32, HB95: American Type Culture Collection, Rockville, Maryland, USA). W6/32 bound to the surface of cultured mesangial cells but did not influence adhesion of cIV. SP2 myeloma culture supernatant was also used as a control.

Immunoprecipitation analysis of integrins from mesangial cell membranes

Mesangial cells metabolically labeled with [ S]-methionine were detached fro flasks by treatment with trypsin (Sigma) for 2 minutes, washed three times with phosphate-buffered saline (pH 7.4) and resuspended in PBS containing protease inhibitors (1 mM PMSF and 1 mM NEM). The radiolabeled cell membrane proteins were solubilized by adding lysis buffer (1% Triton X-100, 1 mM Calcium, 1 mM 10

PMSF, 1 mM NEM and PBS at pH 7.4) and incubating for 60 minutes at 4°C. Insolubl material was separated by centrifugation at 10,000 rpm for 30 minutes.

The supernatant was transferred and 10 μl was tested for radioactivity (> IO⁷ cpm/per antibody being assayed was considered to be adequate for immunoprecipitation). The lysate was precleared once with fetuin-agarose which was removed by centrifugation at 10,000 rpm for 15 minutes. This was followed by three preclears with protein A agarose bound to rabbit anti-mouse IgG, the last preclear was done overnight.

For immunoprecipitation, the cell lysate (equal counts of lysate for cells in 5 an 25 mM glucose were used) was incubated with the monoclonal antibodies to be tested, pre-bound to rabbit anti-mouse protein A-agarose. Myeloma culture supernatant was used as a negative control. Anti-HLA antibody (W6/32) was used as a control for loading. After an overnight incubation at 4°C, the agarose beads were washed five times and bound material was eluted by boiling for 5 minutes in SDS. The eluted material was analyzed by loading lysate from each permutation on a

7.5% non-reducing SDS-PAGE gel and labeled proteins were visualized by autoradiography. The fluorograms were scanned with a Macintosh Quadra 840 computer using the NIH Image 5.1 Program, and the optical density ofthe bands was red after subtracting the background. The O.D. was corrected using the lanes immunoprecipitated with W6/32. Immunoprecipitation assays were performed three times for each growth condition of mesangial cells.

Immunoprecipitates were obtained with anti-integrin monoclonal antibodies from detergent extracts of metabolically labeled human kidney mesangial cells grown i 5 (low) or 25 mM (high) glucose. Equal counts of membrane proteins were immunoprecipitated to compare the level of integrin receptors of mesangial cells under the two growth conditions of low or high glucose levels.

Cells grown in 25 mM glucose have a higher specific activity of labeling than cells in 5 mM glucose. To overcome this difference and permit a comparison ofthe band intensity on immunoprecipitation equal counts of cell lysate from the two populations were immunoprecipitated with the antibody. Densitometry and statistical analysis of three experiments was performed, the data normalized to the HLA control and expressed as an O.D. ratio of cells grown in high glucose (HG) to cells grown in low glucose (LG), for three experiments, with (LG = 1). Cells were labeled with [³⁵S]- methionine, the cells were harvested, and solubilized. Samples were incubated with antibody and equal counts of cell lysate from the two cell populations were immunoprecipitated with equal amounts of antibody. The control indicated that there were comparable amounts of cell surface HLA determinant precipitated from each sample. W6/32, a Mab to cell surface HLA determinant was used as a negative control. Other antibodies used included an anti-αl antibody (TS2/7) and an anti-α2 antibody (P1H5). In total 5 mM and 25 mM glucose exposed cell extracts were immunoprecipitated side by side 3 times. The αl subunit band was clearly discernible at 180 kD in cell samples exposed to 5 mM of glucose and was associated with a βl band (116 kD). No αl band could be seen in the 25 mM treated cell sample. In contrast, the α2 subunit band was more prominent in cell samples exposed to 25 mM glucose and appeared as a band at 130 kD. The 130 kD α2 band was present in 5 mM glucose but was significantly less intense than the 25 mM glucose treated samples.

The cell lysates were also incubated with the following antibodies including: SP2 myeloma culture supernatant; anti-βl (P5D2), anti-β2 (P4H9), anti-α2 (P1H5), anti-α3 (P3D11), anti-α4 (P4G9), anti-α5 (P3D10) and anti-α6 (G0H3). Results were interpreted from three independent experiments. Immunoprecipitation of α3-α6 and βl integrin subunits was performed on cells from the two growth conditions. Subunits α4 and α6 were not detected in either cell population. The antibody to the βl subunit precipitated a 116 kD protein, the βl subunit, and also a precursor βl band at 105 kD. The α3 and α5 subunits were seen at » 130 kD with the associated β subunit at 116 kD, in both cell populations.

Flow cytometry

Cell surface expression of integrin subunits by cultured human mesangial cells was evaluated by indirect immunofluorescence staining and flow cytometry. Mesangial cells were released with trypsin, washed and resuspended in FACS buffer (HBSS, 2% goat serum, 0.02% sodium azide). An equal number of cells, 2 x 10 were added to each vial. The cells were incubated with primary antibody for one hour at 4°C and washed once with 1 ml FACS buffer. The secondary antibody was then added in a total volume of 0.5 ml FACS buffer and incubated for 30 minutes at 4°C. The cells were again washed in 1 ml of FACS buffer and resuspended in 0.5 ml of 2% formaldehyde. The data was analyzed using CONSORT 30 software on a FACScan (Becton

Dickinson, Mountain View, CA). Positive fluorescence was determined on a four decade log scale and fluorescence (log Fl) was expressed as the mean channel number of 5,000 cells. Cell surface expression experiments were performed in duplicate with each antibody, at least three times with each growth condition of mesangial cells. Densitometric scanning ofthe fluorograms generated from metabolically labeled cells indicated that the synthesis ofthe βl (12%), α3 (14%) and α5 (19%) were moderately increased upon growth in 25 mM glucose. Growth in 25 mM glucose dramatically decreased synthesis ofthe αl subunit (39% reduction in intensity) while synthesis of α2 was considerably increased (42%). These changes in metabolic activity were paralleled by a similar change in the cell surface integrin phenotype of mesangial cells grown in high glucose. To assess the effect of different glucose concentrations in the medium on the levels of mesangial cell surface integrin receptor expression cells in each glucose treatment population were stained for immunofluorescence and processed for flow cytommetry. Mean channel fluorescence (MCN) values of integrin subunit expression were obtained from 3 experiments. Within each experiment the ratio of MCN for cells grown in high glucose (HG) to cells grown in low glucose (LG), denominator = 1 was calculated.

Cell surface expression ofthe following integrin subunits was increased by growth in high glucose: βl (24%), α2 (26%), α3 (18%), and α5 (19%). The decrease in the synthesis of αl was reflected in a concomitant decrease in cell surface expression

(33% reduction in specific staining). The α4 and α6 subunits were not detectable in cultured mesangial cells either by immunoprecipitation or flow cytometric analyses.

Mesangial cells grown in high glucose (for at least 2 passages) were returned to control media (5 mM glucose), again for at least 2 passages. A flow cytometric analysis of these cells revealed a reversion to "low glucose" type. The expression of α2, α3, α5 and βl were decreased while the expression of αl increased (data not shown). Example 2

Adhesion of Cultured Mesangial Cells to

Type IV Collagen (cTV.: Effect of High Glucose

Cell adhesion to collagen IV (cIV)

The cells were detached from culture flasks by incubation with trypsin 0.05% and EDTA 0.02% for two minutes at 37°C, then washed twice with DMEM and resuspended to the appropriate concentration in binding buffer (DMEM, 25 mM HEPES, 2 mg/ml BSA at pH 7.4). 48 or 96 well plates were coated overnight at 29°C with cIV in serial dilutions starting from 100 μg/ml (5 μg/96 well or 20 μg/48 well).

Under these conditions approximately 50% ofthe cIV adhered. To block the remaining reactive sites the plates were treated with 200 μl of BSA at 2 mg/ml for 2 hours at 37°C. 50 μl of suspension containing 5000 cells (96 well plates) or 100,000 cells (48 well plates) was added per well. The plates were incubated at 37°C in a humidified incubato for approximately 30 minutes. The non-adherent cells were removed by washing three times with binding buffer and then 100 μl of "lysis" buffer (0.5 NaOH, 1% SDS in distilled water) was added to each well for 30 minutes at 60°C. The lysate was transfened to scintillation vials and counted. The data was expressed as a percentage o the total input cpm. Cell adhesion assays were performed in triplicate, at least three times for each growth condition.

Cells grown in medium containing 25 mM glucose adhered significantly better than cells in 5 mM glucose. Adhesion increased with coating concentration of cIV and was saturated at 25 μg/ml for both cell populations.

Inhibition of cell adhesion with monoclonal antibodies

Since growth in high glucose appeared to alter the synthesis and expression of the integrin receptors αl βl and α2βl which have been reported to be involved in cell adhesion to collagen, (Wayner and Carter, J. Cell. Biol. 105:1873 (1987)), we examined the effects of glucose on the ability of mesangial cells to adhere to cIV. Monoclonal antibody inhibition of S-methionine labeled human mesangial cells grown in 5 mM glucose to cIV was assessed. Briefly, 96 or 48 well plates were coated with 50 or 200 μl of cIV at 2.5 μg/ml, overnight at 29°C The plates were incubated with 2% BSA in PBS to coat remaining reactive sites on plastic for 2 hours, and then hybridoma culture supematant or ascites containing 10 μg/ml of antibody were added to each well, followed immediately by the cells. After 30 minutes non-adherent cells were washed off and adherent cells were quantitated. Results were obtained from 3 experiments. SP2 myeloma culture supematant of W6/32 were used as negative controls. A quantitative ELISA was used to determine the concentration of antibody in the hybridoma culture supematant or ascites.

In each case, the concentration of monoclonal antibody (Mab) was determined relative to a standard curve generated with an isotype-matched control mouse IgG. The concentration of antibody required to saturate the binding sites on human mesangial cells was determined by flow cytometry. The concentration ofthe antibodies used in the inhibition assays were well above the saturating concentration as determined by flo cytometry. Data were expressed as the percent of maximal binding observed in the presence of W6/32 antibody. Inhibition experiments were performed at least three times, in triplicate, for each growth condition with the various antibodies. Mesangial cells grown in high glucose (25 mM) adhered better to cIV than cells grown in low glucose (5 mM). Results indicated that adhesion increased with coating concentration of collagen IV and saturated at about 25 μg/ml for both cell populations.

In order to examine the activity of collagen receptors expressed by mesangial cells grown in high glucose, we performed adhesion experiments in the presence of well characterized neutralizing antibodies directed to various βl integrin subunits. A panel of antibodies was used all of which have been reported to inhibit the adhesion of cells to various substrates (Wayner and Carter, cited supra, 1987; Wayner et al., cited supra, 1993). Antibodies were used at saturating concentrations as determined by immunofluorescence staining and flow cytometry. In the competition experiments, the following criteria were selected to promote half-maximal binding of mesangial cells:

2.5 μg/ml cIV and a short term assay (less than 30 min). The ability of neutralizing Mabs to inhibit mesangial cell adhesion to cIV was examined in low (5 mM) or high glucose (25 mM) containing media.

To test Mab-mediated adhesion inhibition of mesangial cells grown in 5 mM glucose or 25 mM glucose to collagen IV, S-methionine labeled human mesangial cells were seeded in 48 well plates (100,000 cells/well) coated with 200 μl cIV (2.5 μg/ml, ovemight at 29°C). Mab's anti-αl, SR84, anti-α2, P1H5, anti-βl, P5D2 and SR84 and P1H5 together, were added to the wells before seeding with cells. Adhesion in the presence of W6/32 was used as a control. After 20 minutes non-adherent cells were washed out and adherent cells quantitated. The data was expressed as a percentag ofthe binding in the presence of W6/32. and the two cell populations were normalized by using the binding in the presence of HLA antibody to represent 100% and the inhibition by other antibodies was calculated as a percentage of binding in the presence of HLA.

The results indicated that the αl βl integrin receptor had a reduced role (*p < 0.001) for cells grown in 5 mM glucose as compared with 25 mM glucose. Ofth antibodies examined, only Mabs directed to the αl (SR84), α2 (P1H5) or βl (P5D2) integrin subunits inhibited the binding of mesangial cells to cIV. When mesangial cells were grown in either low or high glucose, adhesion to cIV could be almost completely inhibited with Mabs to βl (P5D2) or a combination of αl (SR84) and α2 (P1H5). The relative effects ofthe neutralizing Mabs directed against the αl and α2 subunits varied depending on whether mesangial cells were grown in low or high glucose. In 5 mM glucose the Mab to the αl subunit of integrins resulted in more inhibition (« 50%) than in 25 mM glucose (« 20%) (p < 0.001). This is consistent with the presence of significantly more αl integrin on the surface of cells grown in 5 mM glucose. Altematively, in 5 mM glucose the Mab to the α2 subunit resulted in less inhibition (« 60%) than in 25 mM glucose (* 75%) (p < 0.001). Mab's against the α3, α4, α5 and α6 subunits did not inhibit adhesion (data not shown).

These data demonstrate that under low glucose growth conditions, mesangial cells use αl βl and α2βl integrins to bind cIV coated surfaces. However, cells grown in high glucose, appear to rely more on the α2 subunit complexed with βl . The results of these functional studies are consistent with the observed alterations in the integrin cell surface phenotype discussed in Example 1.

Example 3 Localization of αlβl and α2βl Integrin Receptors Localization of αl integrin in focal adhesions

Glass cover slips were coated with 50 μl of cIV at 2.5 μg/ml, overnight at 29°C

The coated areas were "blocked" for two hours with BSA at 2 mg/ml, in PBS. Human mesangial cells were processed as before, seeded on each spot of cIV in 50 μl of bindin buffer (2500 cells) and allowed to adhere for 5 hours at 37°C. The unbound cells were washed off with PBS. Adherent cells were fixed with 2% paraformaldehyde in HBSS for 30 minutes followed by permeabilization with 0.5% Triton X-100 for 2 minutes. The cells were blocked again with PBS following which 200 μl of hybridoma culture supematant containing anti-αl antibody (TS1/7) was added to each spot and incubated at room temperature for 1 hour. The coverslips were then thoroughly washed and rhodamine-conj ugated goat anti-mouse antibody (1:100) (Boehringer Mannheim, Indianapolis, IN) was added for one hour. The coverslips were again washed and incubated with anti- vinculin antibodies (Sigma, St. Louis, MO) preconjugated

(Quicktag, FITC labeling kit, Boehringer Mannheim, Indianapolis, IN) to FITC labeled goat anti-mouse antibody for 1 hour at room temperature. The coverslips were finally washed, mounted on glass slides and viewed for focal adhesions by co-localization of vinculin with αl integrin.

Staining of normal human adult kidneys for the presence of βl integrins

Normal human adult kidney tissue was snap frozen in liquid nitrogen and sections were prepared with a cryostat at 5 μm intervals. The sections were stained using an anti-mouse Vectastain Elite Kit (as described by Wayner et al., 1993) with diamino benzene (DAB) as the chromogen. The following mAbs were used: αl

(TS2/7), α2 (P1H5), α3 (P3D11), α4 (P4G9) and βl (P5D2). These monoclonal antibodies are available from the following sources and stained the following histological areas as was demonstrated in these studies: αl (TS2/7) Martin Hemler, Dana Farber Cancer Center, Boston, MA. Stained mesangium.

α2 (P1H5) EA Wayner, Fred Hutchinson Cancer Center, Seattle, WA

Stained mesangium.

α3 (P3D 11 ) EA Wayner, Fred Hutchinson Cancer Center, Seattle, WA

Stained the mesangium, endothelium, visceral and Bowman's epithelium and capsule.

α4 (P4G9) EA Wayner, Fred Hutchinson Cancer Center, Seattle, WA

Did not stain glomeruli. β 1 (P5D2) EA Wayner, Fred Hutchinson Cancer Center, Seattle, WA

Stained mesangium, endothelium, visceral epithelium, Bownman's epithelium and capsule.

Normal mouse IgG (all isotypes) was used as a negative control.

These studies demonstrated the presence of αlβl and α2βl integrin receptors in focal adhesions. Focal adhesions are observed when cells spread in culture on matrix components such as collagen IV, fibronectin or laminin. Integrins cluster at the site of focal adhesions on the cell surface with intracellular fibers such as vinculin staining at these locations within the cell periphery, (see Hynes, et al. CeU 69:11-25, 1992 and Burridge, et al. Ann. Rev. CellBiol. 4:487-525, 1988). This supports the hypothesis that mesangial cells use αlβl and α2βl integrin receptors to bind to cIV. It has been well established that when a particular integrin receptor is engaged by a specific ligand it can be detected in focal contacts co-localized with certain components ofthe cytoskeleton such as vinculin. Therefore, we asked whether mesangial cells could localize αl (or α2 and βl) to focal adhesions when seeded on cIV coated substrates. α2 or βl could be detected in focal contacts on cIV regardless of whether mesangial cells were grown in either low or high glucose. Additionally, when mesangial cells were grown in 5 mM glucose and subsequently seeded on cIV coated surfaces, αl could also be co-localized with vinculin within several focal contacts by dual-label immunofluorescence staining. It is believed that cIV binding in cells maintained in low glucose engages both the αl and α2 subunits. αl could be detected in only some ofthe focal adhesions stained by vinculin. As a control, αl was not detected in focal contacts when mesangial cells were seeded onto fibronectin coated surfaces regardless ofthe glucose concentration ofthe cell culture media.

Immunohistochemical staining of integrin receptor subunits in normal human adult and fetal kidney revealed that both αl and α2 could be localized within the mesangium. The αl receptor was diffusely expressed throughout the mesangium whereas the distribution of α2 was more limited and focal. Also consistent with the results we obtained with cultured mesangial cells, βl and α3 were intensely expressed throughout the mesangium, while α4 could not be detected in either fetal or adult mesangium. Example 4

Alterations in RNA Production in Human Mesangial Cells cultured in High and Low Glucose Concentrations Our efforts have concentrated on finding a way to predict, at early stages after the onset of diabetes, the subjects who will later develop nephropathy. We focused on a major hallmark of diabetic nephropathy, that of mesangial expansion. We first examined mesangial cells in culture, since these cells secrete their surrounding matrix, which is expanded in diabetes; however, biopsied tissue can be treated in the same manner, as will be understood by those skilled in the art. The matrix consists primarily of collagen IV.

Primary cultures of human mesangial cells undergo several phenotypic changes in response to elevated glucose concentrations and glucose-modified ("glycated") collagen IV. These changes included altered cell interactions with the collagen matrix. In elevated glucose concentrations, the αl subunit underwent a substantial decrease, concomitant with an increase ofthe α2 integrin subunit. This change was observed wit immunoprecipitation and flow cytometry. Further studies with Northern analysis and in situ hybridization ofthe cultured mesangial cells confirmed the integrin reversal. In the studies employing Northern analyses, separate samples of total RNA were isolated from the mesangial cells on each culture plate or altematively from rat kidneys (see Example 5, below) by a single-step method using RNA STAT-60 isolation reagent (TEL-TES "B", INC., Friendswood, TX) according to the manufacturers directions. Briefly, the cells were lysed with RNA STAT-60™ solution by repetitive pipetting; the tissues were cut into small pieces and homogenized in the RNA STAT-60 solution with a high-speed tissue homogenizer (Polytron CH6005, Luzern, Switzerland). The nucleic acid mixture was extracted with 0.2 ml chloroform per lml ofthe RNA STAT-60 solution. Total RNA was precipitated for 10 min at -80°C in isopropanol, and the pelleted RNA was redissolved in TE buffer. The total RNA was free of DNA and proteins and had a 260/280 wavelength ratio > 1.8. Northern blot analysis-T e, RNA samples were denatured in formaldehyde gel- running buffer (20 mM MOPS, 8 mM sodium acetate, mM EDTA, at pH 7.0) containing 6% formaldehyde and 50% formamide by heating at 65°C for 15 min. For each sample 20 mg of RNA was mixed with 6x loading buffer (50% glycerol, 1 mM EDTA, 0.25% bromphenol blue, 0.25% Xylene cyanol FF), loaded on a 1% agarose gel submerged in 6% formaldehyde running buffer, and run at 3-5 V/cm for 3-4 hours. RNA was transfened from the agarose gel to a nylon membrane (Boehringer Mannheim, Indianapolis, IN) by capillary elution and immobilized by UV cross-linking (Stratalinker UV; Stratagene, La Jolla, CA). The membranes were then incubated in prehybridization solution containing 50% formamide, 5xSSC 0.02% SDS, 0.1% N- lauroylsarcosine, 2% blocking reagent (Boehringer Mannheim), and 20 mM sodium maleate (pH 7.5) for >3 hours at 42°C Radiolabeled probes (see Example 5) for the integrin subunits or controls were then added to the prehybridization solution and hybridization was performed overnight at 42°C (for cDNA probe) or 50°C (for antisense RNA probe). After hybridization, the membranes were initially washed in 2x SSC, 0.05% SDS for 10 minutes at room temperature and then washed for an additional 40 minutes at 42°C (for cDNA probe) or 60°C (for antisense RNA probe). Membranes were then exposed to X-ray film (X-Omat RP; Eastman Kodak Co., Rochester, NY) for 1 day at -80°C. After being stripped of previous probes by heating in 0.2x SSC, 0.5%

SDS for 10 min at 100°C, the membranes were reprobed as described above. Images of autoradiograms were captured and digitized using a CCD video camera module interfaced with a microcomputer (Macintosh Ilex: Apple Computers Inc., Cupertino, CA) and analyzed using image processing software (NIH Image 1.55b77: public domain).

Cells grown in 25 mM glucose expressed lower levels of αl integrin than seen in an equivalent amount of RNA from cells grown in 5 mM glucose. Densitometric analysis demonstrated an «30% decrease upon averaging the values from four samples. Similar analysis demonstrated «30% increase in α2 integrin expression in cells grown in 25 mM glucose.

Example 5 In Situ Hybridization Detecting Expression of Integrins in Kidney Sections Taken at Various Times After Onset of Diabetes

The expression of αl and α2 integrin receptors was examined in rat kidney sections after the onset of diabetes. The in situ hybridization approach was used to examine kidney sections of streptozotocin-diabetic rats, 2.5 months after induction of diabetes. At this time interval, glomerular changes were still minimal. The streptozotocin-induced diabetic rat model mimics human changes of mesangial expansion and glomerular basement membrane thickening in late nephropathy and is an art accepted model for diabetes and nephropathy.

Female non-pregnant Sprague-Dawley rats were obtained from Brithwood, Minneapolis, MN. The animals weighed 190-210 g at the beginning ofthe experiments and were given a 52mg/kg intraperitoneal dose of streptozotocin (STZ, Zanazar brand, Upjohn Corp., Kalamazoo, Ml) in calcium citrate and calcium carbonate Buffer (pH

4.5) to induce diabetes, while the controls were injected with the same amount of Hanks' balanced salt solution (pH 7.2). The animals were fed on standard rat chow (Purina laboratory chow # 5001. RFG PET@Supply Company, Plymouth, MN), and tap water ad libitum. Presence of diabetes was confirmed by detection of >400mg/dl nonfasting plasma glucose levels 10 days post injection by tail vein bleeding using the glucose peroxide method (Beckman glucose analyzer, Beckman Instruments, Inc., Fullerton, CA).

Body weight was determined weekly, blood glucose levels were determined at 4 weeks after induction of diabetes, and on the day before the termination ofthe experiment, which was 2.5 month from induction of diabetes. Urinary albumin excretion (UAE) was determined by radial immunodiffusion Mancini method, using goat IgG fraction against rat albumin (Cappel Cat. No. 55727) and purified rat albumin (Cappel Cat. No. 55952, Cappel Research Products, Durham, NC), according to previously published procedures (Mauer et al, Diabetes 27:959-64, 1978). Rats were sacrificed at 2.5 months after diabetes induction and kidney tissue was perfusionally fixed by injecting freshly prepared 4% paraformaldehyde through the renal artery. This was followed by ovemight fixation in 4% paraformaldehyde after removal from the body. The tissue was sectioned at 5 μm and placed on the silane-coated slides (Digene Diagnostics, Inc., Beltsville, MD) for in situ hybridization with probes for the αl and α2 integrin subunits.

2.5 months after injection of STZ, diabetic rats weighted significantly less than controls, whereas their right kidney weight and serum glucose concentration were significantly increased, as compared to the controls (see Table 1). Diabetic and non¬ diabetic rats demonstrated no significant difference in glomerular size and albumin excretion at 2.5 month after induction of diabetes (Table 1).

TABLE 1

TISSUE €O TROL DIABETIC m$

Body Wt(g) 390+/-10 200+/-20 S

Right Kidney wt. (g) 1.35+/-0.1 1.8+/-0.1 S

Plasma glucose (mg/dl) 140+/-25 760+/150 s

Glomerular area 1.42+/-0.5 1.45+/-0.6 NS

A 5.4 kb human α2 integrin CDNA clone (Takada, et al., 1989, supra) and a rat αl integrin cDNA clone (Ignatius et al, supra) in bluescript vector (Stratagene, La Jolla, CA) were used in these experiments. A 1.79 kb α2 integrin cDNA fragment was restriction digested from the EcoRI site. Similarly, a 3.98 kb αl integrin cDNA fragment was obtained by restriction digestion from the EcoRI site. cDNA fragments were purified by GENE CLEAN II kit (BIO 101, San Diego, CA) and labeled using the random primer labeling kit (Boehringer Mannheim, Indianapolis, IN) with P³²-dCTP (NEN) for Northem blotting and with S³⁵-dCTP (NEN for in situ hybridization. GAPDH and sheep visna vims cDNA (PLV-KS) (Staskus et al, Virology 181 :228-240, 1991 ) probes were used as the positive and negative controls respectively. The probes preferably had a specific activity of 2 x 10 - 1 x 10 dpm/μg.

By Northem blotting, compared to the controls, the diabetic kidneys expressed 113.5% more αl(IV) RNA, 46.5% more α3(IV) RNA, 54.8% less metalloproteinase-2 RNA (MMP-2, an enzyme that cleaves type IV collagen) and 246% more TIMP-l RNA (a tissue inhibitor of metalloproteinases) with a p< 0.01 in all cases as determined by ANOVA.

The expression of αl and α2 integrin RNA was localized using a modification o a previously described method for in situ hybridization (Staskus et al. supra). 5μm tissue sections on silane-coated slides were fixed in the freshly prepared 4% paraformaldehyde for 10 min. The slides were pretreated with 0.2N HCl for 20 min, 0.

15 M Triethanolamine (TEA, Sigma, St. Louis, MO) for 15 min, 0.005% digitonin for 5 min, 3 mg/ml proteinase K (Sigma) for 15 min at 37°C, and O.3% acetic anhydride - O.IM TEA for 10 min. Hybridizations were performed under stringent hybridization conditions. Stringent hybridization conditions are defined in this specification as 50°C overnight, in 50% formamide, 0.6 M NaCl, lx Denhardt's solution, 0. 17 mg/ml human COT^RT DNA (GIBCO/BRL), 1 mg/ml poly A (Boehringer Mannhieim), 10% (w/v) Dextran sulfate (Sigma), 0. 1 M dithiothreitol (DTT, Boehringer Mannheim), 1 mM

EDTA, 0. 1 mM aurinitricarboxylic acid (ATA, Sigma) and S³⁵-dCTP labeled cDNA probe. The next day, the slides were washed in 2x SSC-0.05% SDS for 60 min at 55°C (recipes for SSC and the like can be found in Sambrook, et al., supra); further washed in a high stringency washing buffer containing 50% formamide, 0.6 M NaCl, 1 mM EDTA, 5 mM DTT and 10 mM Hepes for 4 days at room temperature. After a brief rinse in 2x SSC, the slides were dehydrated in graded ethanol with 0.3 M ammonium acetate then dipped in Kodak NTB-2 emulsion and exposed for 5 days at 4°C

After development the slides were stained with hematoxylin-eosin (Surgipath Canada, Inc., Winnipeg, Canada) and mounted. A ratio ofthe number of silver grains per cell was used to quantitate the results of in situ hybridization. Twenty glomeruli each were counted from each control and diabetic animal. Each glomerulus was assessed for: 1) glomerular area; 2) glomerular perimeter; 3) grains per glomerulus; and 4) number of cell nuclei per glomerulus.

The results were estimated as grains per cell nucleus and grains per glomerular area, as mean +/- SD of 5 animals (20 glomeruli each). (Haase, A.T., [1990]: In situ hybridization. CRC Press, 199-217; Nuovo, G.J., [1992] PCR in situ hybridization, protocols and applications. Raven Press). Groups were compared with the 2-tailed student t-test. Differences between groups were considered significant at p<0.05. The results are illustrated in Fig. 1. Early after induction of experimental diabetes, the expression ofthe αl integrin subunit by glomerular cells was decreased compared to the control, whereas the expression of α2 integrin was increased. The average counts, in diabetic glomeruli hybridized with the αl integrin probe, were significantly lower than control (Fig. 1). Also, the average counts, in diabetic glomeruli hybridized with the α2 integrin probe, were significantly higher than control (Fig. 1). Control animals at 2.5 month diabetes expressed on an average a significantly higher level of αl subunit integrin and significantly lower levels of α2 subunit integrin using unbiased methods of selection of areas for study. The entire section was surveyed for RNA grains, the regions ofthe Bowman's space and the background count were excluded by studying a commensurate area ofthe negative control stained tissue. Compared to the control, glomerular cells (G endothelial, epithelial and mesangial combine) and or tubular (proximal and distal epithelial) cells (TC) had 36% (GC) less grains for αl integrin; 86.4% (GC) more grains for α2 integrin; 82(TC)-167

(GC) more grains for αl(IV); 107 (TC)-137% (GC) more grains for α3(IV); 63.6(GC)- 65.3%(TC) less MMP-2.

The results ofthe present study clearly demonstrate that mesangial cells, when cultured in high glucose (25 mM) instead of normal/low glucose (5 mM) alter their RNA production for the integrin subunits αl and α2. Thus, this phenomenon is observed both at the level of protein and RNA production.

Furthermore, the results of our in situ hybridization and immunohistochemical staining experiments show that these changes can be detected in the mesangium of diabetic rat kidney and that human α2 integrin subunit probes and rat αl integrin subunit probes are functional in both rat and human cells. Work by Mendrick and co¬ workers (Lab. Invest. 72(3):367-375, 1995) has shown that in the rat both integrins αlβl and α2βl of mesangial cells interact with collagen; as happens in the human mesangial cells. In the present study, the distribution of αl and α2 integrin receptor subunit RNA was precisely localized by in situ hybridization to the different cell types ofthe glomerulus and sunounding tubules. Normal rat tissues expressed levels ofthe αl subunit and also the α2 subunit RNA, as determined by counting the number ratio of silver grains/cell. However, the streptozotocin-induced diabetic animals had significantly lower levels of RNA for the αl subunit and significantly higher levels of α2 subunit. A similar distribution of αl and α2 subunit RNA (silver grains) was seen in the proximal and distal tubular epithelial cells. These data indicate that the distribution of cell surface integrin expression may be regulated by gene expression at the transcriptional level.

In summary, using in situ hybridization, similar results were seen in both mesangial cells in vitro and in glomeruli from tissue sections probed for the αl and α2 integrin.

Early after induction of streptozotocin-diabetes in rates, substantial matrix- related gene expression changes occuned. For example, αl and α2 integrin levels changes, components of αlβl and α2βl integrin cell receptors for tlV (an important component ofthe renal extracellular matrix) underwent a reversal in levels with less αl and more α2 integrin being present in glomeruli from kidneys of diabetic rats, when compared to the control. Expression of tlV was increased whereas the expression of MMP-2 which degrades tlV was substantially decreased. TIMP-l, an inhibitor of

MMP-2 was increased. The observed matrix changes indicate an imbalance of tlV synthesis and turnover. This dysmetabolism of tlV, apparent in both the glomemlar and tubular areas ofthe kidney, occurred before significant renal functional changes, or matrix accumulation out of proportion to renal enlargement, could be detectable. These changes could have a regulatory role in significant basement membrane thickening and mesangial expansion of diabetic nephropathy.

Collectively, the obtained data indicate that increased glucose concentration induces quantitative changes in receptor synthesis and cell surface integrin expression of human mesangial cells. In the diabetic, all cell systems are exposed to hyperglycemia and it is know that many cell and organ systems are affected by the disease; therefore, other cell types could similarly be used to assess changes in the levels of αl and/or α2 integrin subunit expression as a measure of a predisposition to a variety of diabetic- induced pathologies. Kyu- Jin, et al. (supra) have noted alterations in integrin subunit expression in skin fibroblasts of diabetic patients. This information, in conjunction with the data discussed herein, indicates that altered levels of integrin subunit expression can be detected from a variety of integrin-expressing cells in diabetic nephropathy patients.

These results support the in vitro primary human mesangial cell culture data demonstrating that changes in cell surface integrin expression indicate the onset of nephropathic changes.

Example 6

Detection of Altered Levels of αl and α2 Integrin Subunit

Expression in Humans using Blood and Tissue Samples

Patients with insulin-dependent diabetes mellitus (IDDM), individuals at risk for developing IDDM, patients with clinical diabetes nephropathy and healthy age matched volunteers are selected for studies to confirm the presence of altered αl and α2 integrin subunit expression in integrin-producing cells. Clinical diabetic nephropathy is defined by the presence of persistent proteinuria (urinary AER > 300 μg/day) in sterile urine of patients with >10 yr duration of disease and concomitant retinopathy and is confirmed by the presence of classic glomerulosclerotic lesions on renal biopsy. Normal, nondiabetic individuals without a family history of hypertension serve as control subjects. Patients were biopsied as follows: For skin biopsies, a biopsy is taken from the anterior surface ofthe left forearm by excision under local anaesthetic such as ethyl chloride, see Trevisan, et al. Diabetes 41 : 1239-45, 1992. The biopsy is optionally divided in half. With half of the tissue frozen immediately in liquid nitrogen and the other half placed in Hanks balanced salt solution. The frozen tissue is embedded in paraffin and processed for in situ hybridization as has been described above. A portion ofthe intact tissue is preferably immediately minced and processed for RNA isolation using techniques described above. Remaining minced tissue is gently digested with trypsin to obtain a cell suspension, washed in media containing serum to remove trypsin and plated onto tissue culture dishes containing 10% FCS supplemented DMEM with antibiotics.

Renal biopsies were obtained as follows. Patients should have normal blood pressures, normal coagulation values and platelet counts. Ultrasound was used to precisely localize the kidney. Ultrasound was also used to determine renal size, structural defects and post-void residual urine. Renal biopsies were performed on sedated patients using the Franklin modified Vim-Silverman or Truecut needles available from surgical supply suppliers. The biopsy specimens were immediately examined under a dissecting microscope to ensure that adequate samples of glomeruli were present for subsequent studies to quantitate integrin levels. Biopsied tissue was sectioned and processed for in situ hybridization as described in Example 5. In one example, renal samples from diabetic patients who did not show signs of microalbuminuria, but who had diabetic siblings with renal nephropathy were processed for in situ hybridization and PCR in situ hybridization. Renal samples from diabetic patients without a family history of nephropathy were also studied by PCR in situ hybridization to detect altered levels of integrin subunit expression. PCR in situ hybridization is performed as follows. Sections are fixed as described in Example 5 and rinsed in RNase free water. The protocol used is that described by Nuovo, et al. (Am. J. Surg. Pathol. 17:683-690, 1993.) Cells are treated with pepsin and DNase as described. cDNA synthesis is initiated by adding lOμl of a solution containing one or more ofthe following probes listed in a 5 '-3' orientation with their SEQ ID NOS and their nucleic acid location on the respective integrin gene with reverse transcriptase (Perkin-ELmer, Norwalk, Conn.):

αl integrin primer SEQ ID NO NA location

CCAGAGTCACTCTCACAGAG 5 2729-2748

CACAGCGTACACGTACACC 6 1991-2009

CACTTATAGACATCTCCAG 7 646-664 α2 integrin primer SEQ ID NO NA location

CATCCATGTTGATGTCTG 8 1733-1750 CATGTGATTCACCGTCAG 9 894-910 GCATATTGAATTGCTCCGAATGT TGG 10 801-826

The resulting cDNAs are subjected to amplification containing a 1 μM concentration (each) of one or more ofthe above primers with a paired primer located 5' to the primers provided above. Those skilled in the art will recognize that a variety of other primers could also be used from the αl and α2 integrin gene sequence to similarly perform PCR in situ hybridization. The prefened primers paired with the above primers are provided below.

αl integrin primer SEQ ID NO NA location SEQ ID Pair GGCGTATGCACAACGCA 11 2261-2277 5

GCGACAGCTGACCAGTCAGCA 12 1509-1529 6 CACTCCTCCACAGCTCCT 13 251-268 7

q2 integrin primer SEQ ID NO NA location SEQ ID Pair ACATGTACTCACTGG 14 1593-1608 8

CTCACATGTGGTCCTCTG 15 433-451 9 GTCCTGTTGACCTATCCACTGC 16 296-319 10

The SEQ ID Pair in the above table refers to the paired primer that provides amplification ofthe sequence positioned between the primer pairs on the respective integrin gene. The PCR products are detected by using an antidigoxigenin-alkaline phosphatase conjugate and the chromagen nitroblue tetrazolium (NBT)-5-bromo-4- chloro-3-indoylphosphate toluidinium (Salt) (BCIP). The counterstain nuclear fast red is used to stain nuclei. Internal probes located within the nucleic acid regions amplified by PCR can also be used to identify the amplified fragments. Thus, based on the pairings provided above, oligonucleotide probes can be selected between regions 267- 645, 1530-1990 and between 2278-2728 for the αl integrin gene and between regions 320-800, 452-893, 1607-1732 for the α2 integrin gene and hybridized and stained following the in situ hybridization methods detailed in Example 5.

A blood sample is also taken from the patient and leukocytes are isolated from blood by centrifugation, followed by hypotonic shock of residual blood cells. The leukocytes are then processed for in situ hybridization as has been discussed in the preceding examples.

Results:

PCR in situ hybridization with renal tissues demonstrated decreased αl and increased α2 integrin subunits in the patient with diabetic neuropathy as compared with control tissue.

Quantitative analysis of RNA grains per unit area of kidney glomeruli and tubules was performed by counting silver grains under epi-polarized light.

As shown in Table 2, both glomeruli and tubules ofthe diabetic neuropathy patient showed significantly decreased αl integrin levels as compared to the control, whereas α2 integrin levels were significantly increased as compared with control levels.

TABLE 2

Glomeruli³ Tubules³

Sample αl α2 αl α2

Control 156 83 136 101

Diabetic Neuropathy 121^b 95^c 89^c 124^{b a} = grains per unit area ^b = p <0.05 ^c = p <0.01

These results confirm the in vitro observations in mesangial cells that there is a decrease ofthe αl integrin subunit and a concommitant increase of α2 integrin expression in a diabetic nephropathy. This represents a reversal of mesangial integrins which mediate binding of mesangial cells to collagen IV.

Example 7 Increased Integrin Subunit Expression in Skin Fibroblasts

From Diabetic Patients with Nephropathy as Compared with Control Diabetic Patients

Fibroblasts were obtained from skin biopsies from diabetic patients with or without diabetic nephropathy and cultured as described for Example 6. Expression of α3, α5, and beta-1 integrin subunits in the cultured cells was analyzed by Northem blotting and subsequent densitometry, as described above, and using published probes. For the α3 integrin subunit, the 1.9 Sail fragment described in Takada Y., et al., J. Cell Biol. 115:257-266 was used. For the βl subunit, the 3.6 kb insert ofthe βl subunit (the whole cDNA), described in Giancotti and Ruoslahti, Cell 60:849-850 (1990) was used. For the α5 subunit, the 3.7 kb Sall-Xba insert ofthe α5 subunit (the whole cDNA) described in Giancotti and Ruoslahti, Supra as used. These probes were radiolabeled and used under the same conditions as those described for Example 6.

The study included five patients per group, five each from the normal, diabetic "slow track" and from the Diabetic "fast track". Both groups of diabetic human subjects had renal function studies and kidney biopsies performed as part of their evaluation as possible candidates for pancreas transplantation. All procedures were approved by the Committee on Human Subjects at the University of Minnesota, and all patients gave written consent. All patients spent one week at the Clinical Research Center (CRC) at the University of Minnesota for pre-pancreas transplant evaluation, during which time they underwent multiple 24-hour urine collections (at least three) for measurements of creatinine clearance and urinary albumin excretion. Blood pressure was measured repeatedly by the CRC nursing staff. HbAl was used to assess glycemic control. All patients underwent percutaneous kidney biopsy and skin biopsy. Patients were divided into two groups based on criteria of severity of renal lesions determined by morphometric analysis of mesangial functional volume and IDDM duration.

"Normal" samples were kidney biopsies from non-diabetic human subjects, taken to examine for the presence of neoplastic tissue, etc., on which a similar analysis to that performed for the diabetic tissues was done. These subjects underwent similar renal functional studies to make certain that albuminuria, increased creatinine clearance, or hypertension were not present.

The data, shown below in Table 3, demonstrate a significant increase in α3 and beta-1 subunit expression in the skin fibroblasts of diabetic nephropathy patients as compared with the control diabetic patients.

TABLE 3

Integrin Normal Control Nephropathy P Subunit Values Diabetic Diabetics α3 11.5 10.1 17.1 <0.5 ( 9.1-13.3) ( 8.6-12.8) (16.1-35.6)

α5 36.2 38.7 30.3 (18.3-46.6) (31.6-57.2) (13.2-48.4)

bl 29.9 24.9 37.1 <0.5 (24.0-33.4) (17.4-30.9) (24.2-74.6)

While particular embodiments ofthe invention have been described in detail, it will be apparent to those skilled in the art, that these embodiments are exemplary rather than limiting, and the true scope ofthe invention is that defined in the following claims.

SEQUENCE LISTING

(1) GENERAL INFORMATION

(i) APPLICANT: Regents of the University of Minnesota

(ii) TITLE OF THE INVENTION: ANALYSIS OF ALPHA INTEGRINS FOR THE DIAGNOSIS OF DIABETIC NEPHROPATHY

(iii) NUMBER OF SEQUENCES: 16

(iv) CORRESPONDENCE ADDRESS:

(A) ADDRESSEE: Merchant & Gould

(B) STREET: 3100 Norwest Center

90 South 7th Street

(C) CITY: Minneapolis

(D) STATE: MN

(E) COUNTRY: US

(F) ZIP: 55402

(v) COMPUTER READABLE FORM:

(A) MEDIUM TYPE: Diskette

(B) COMPUTER: IBM Compatible

(C) OPERATING SYSTEM: DOS

(D) SOFTWARE: FastSEQ Version 1.5

(vi) CURRENT APPLICATION DATA:

(A) APPLICATION NUMBER: Unknown

(B) FILING DATE:

(C) CLASSIFICATION:

(vii) PRIOR APPLICATION DATA:

(A) APPLICATION NUMBER:

(B) FILING DATE:

(viii) ATTORNEY/ GENT INFORMATION:

(A) NAME: Kettelberger, Denise

(B) REGISTRATION NUMBER: 33,924

(C) REFERENCE/DOCKET NUMBER: 600.314USWO

(ix) TELECOMMUNICATION INFORMATION:

(A) TELEPHONE: 612-332-5300

(B) TELEFAX: 612-332-9081

(C) TELEX: (2) INFORMATION FOR SEQ ID NO:1:

(i) SEQUENCE CHARACTERISTICS:

(A) LENGTH: 3987 base pairs

(B) TYPE: nucleic acid

(C) STRANDEDNESS: single

(D) TOPOLOGY: linear

(ii) MOLECULE TYPE: Genomic DNA

(iii) HYPOTHETICAL: NO

(iv) ANTISENSE: NO

(v) FRAGMENT TYPE:

(vi) ORIGINAL SOURCE:

(ix) FEATURE:

(A) NAME/KEY: CDS

(B) LOCATION: 420...3959

(A) NAME/KEY: mat_peptide

(B) LOCATION: 504

(D) OTHER INFORMATION:

(xi) SEQUENCE DESCRIPTION: SEQ ID NO:l:

AGTATGGAGA GAAGGTCGTT TAAAAAGGCA GATGTCCCTT TAAGGTTTGC TTTGCTGCTG 60

CCCGTGGACT TTAGCCTAAA CAGGGTCCCG CGAAGTTGGC TTTATTTGTC CATGTCTCGG 120

ACACAGCCTG GGTAGCTGCC AGTGAGATTT CAGGGACGGA GCGCGCAAAG GGGGGGGAAA 180

TGTGGCAATC CATCTGGGAT GTGAGACGCG TGGAGAGGGC TTAGCAGCAT TTGACCAAAA 240

CACAGGAAAT CACTCCTCCA CAGCTCCTGG GCGCAGCAGC GGCTGGGGCC ACTGCCGGAC 300

ACCCTCGGAG ACCACACGAG TGACCCAGAG CGCAAGTCGC CAGCGTCCCG GTTCTGCCTG 360

TTCCTGCCAG CTCCTGCCCA CGAACCGGCA CGTAGCTGGT TCCAGCAGCC GCTCCAGCA 419

ATG GTC CCC AGG CGT CCT GCC AGC CTA GAG GTC ACT GTA GCC TGC ATA 467 Met Val Pro Arg Arg Pro Ala Ser Leu Glu Val Thr Val Ala Cys Ile -28 -25 -20 -15

TGG CTT CTC ACG GTC ATC CTA GGC TTC TGC GTC TCC TTC AAT GTT GAT 515 Trp Leu Leu Thr Val Ile Leu Gly Phe Cys Val Ser Phe Asn Val Asp -10 -5 1

GTG AAA AAC TCA ATG AGT TTC AGT GGC CCA GTA GAG GAC ATG TTT GGA 563 Val Lys Asn Ser Met Ser Phe Ser Gly Pro Val Glu Asp Met Phe Gly 5 10 15 20

TAC ACT GTT CAA CAA TAT GAA AAC GAA GAA GGC AAA TGG GTT CTT ATT 611 Tyr Thr Val Gin Gin Tyr Glu Asn Glu Glu Gly Lys Trp Val Leu Ile 25 30 35

GGT TCT CCT TTA GTT GGC CAA CCC AAA GCA AGA ACT GGA GAT GTC TAT 659 Gly Ser Pro Leu Val Gly Gin Pro Lys Ala Arg Thr Gly Asp Val Tyr 40 45 50

AAG TGT CCG GTT GGG AGA GAG AGA GCA ATG CCT TGC GTG AAG TTG GAC 707 Lys Cys Pro Val Gly Arg Glu Arg Ala Met Pro Cys Val Lys Leu Asp 55 60 65 TTG CCA GTT AAC ACA TCG ATC CCC AAT GTC ACA GAA ATA AAG GAA AAC 755 Glu Pro Val Asn Thr Ser Ile Pro Asn Val Thr Glu Ile Lys Glu Asn 70 75 80

ATG ACA TTT GGA TCA ACT TTA GTC ACC AAC CCG AAT GGA GGA TTT CTG 803 Met Thr Phe Gly Ser Thr Leu Val Thr Asn Pro Asn Gly Gly Phe Leu 85 90 95 100

GCA TGT GGG CCC TTG TAT GCC TAT AGA TGT GGA CAT TTG CAT TAT ACA 851 Ala Cys Gly Pro Leu Tyr Ala Tyr Arg Cys Gly His Leu His Tyr Thr 105 110 115

ACT GGA ATA TGT TCT GAT GTC AGT CCT ACA TTT CAA GTT GTG AAC TCC 899 Thr Gly Ile Cys Ser Asp Val Ser Pro Thr Phe Gin Val Val Asn Ser 120 125 130

TTT GCC CCT GTA CAA GAA TGC AGC ACC CAG CTG GAC ATA GTC ATC GTC 947 Phe Ala Pro Val Gin Glu Cys Ser Thr Gin Leu Asp Ile Val Ile Val 135 140 145

CTG GAT GGC TCC AAC AGC ATC TAC CCC TGG GAA AGT GTC ATC GCC TTT 995 Leu Asp Gly Ser Asn Ser Ile Tyr Pro Trp Glu Ser Val Ile Ala Phe 150 155 160

TTA AAC GAC CTT CTT AAG AGG ATG GAT ATT GGC CCT AAG CAG ACA CAG 1043 Leu Asn Asp Leu Leu Lys Arg Met Asp Ile Gly Pro Lys Gin Thr Gin 165 170 175 180

GTC GGG ATT GTA CAG TAT GGA GAG AAT GTA ACC CAT GAG TTC AAC CTC 1091 Val Gly Ile Val Gin Tyr Gly Glu Asn Val Thr His Glu Phe Asn Leu 185 190 195

AAT AAG TAT TCA TCC ACA GAA GAG GTC CTT GTC GCA GCA AAC AAA ATA 1139 Asn Lys Tyr Ser Ser Thr Glu Glu Val Leu Val Ala Ala Asn Lys Ile 200 205 210

GGC CGA CAG GGA GGC CTC CAA ACG ATG ACA GCC CTT GGA ATA GAC ACA 1187 Gly Arg Gin Gly Gly Leu Gin Thr Met Thr Ala Leu Gly Ile Asp Thr 215 220 225

GCC AGG AAA GAG GCA TTC ACT GAA GCT CGG GGT GCC AGG AGG GGA GTT 1235 Ala Arg Lys Glu Ala Phe Thr Glu Ala Arg Gly Ala Arg Arg Gly Val 230 235 240

AAA AAA GTC ATG GTT ATT GTG ACC GAC GGA GAA TCG CAT GAC AAC TAT 1283 Lys Lys Val Met Val Ile Val Thr Asp Gly Glu Ser His Asp Asn Tyr 245 250 255 260

CGC TGA AAC AGG TCA TCC AAG ACT GCG AGG ACG AAA ACA TTC AGC GAT 1331 Arg Leu Lys Gin Val Ile Gin Asp Cys Glu Asp Glu Asn Ile Gin Arg 265 270 275

TTT TCC ATA GCT ATC CTT GGC CAC TAT AAC AGG GGG AAC TTA AGC ACT 1379 Phe Ser Ile Ala Ile Leu Gly His Tyr Asn Arg Gly Asn Leu Ser Thr 280 285 290 GAA AAA TTT GTG GAG GAA ATA AAA TCG ATC GCA AGC GAG CCC ACG GAA 1427 Glu Lys Phe Val Glu Glu Ile Lys Ser Ile Ala Ser Glu Pro Thr Glu 295 300 305

AAG CAC TTC TTC AAT GTC TCG GAT GAG TTG GCC CTG GTC ACT ATT GTT 1475 Lys His Phe Phe Asn Val Ser Asp Glu Leu Ala Leu Val Thr Ile Val 310 315 320

AAA GCT CTG GGA GAA AGG ATA TTC GCT TTG GAA GCG ACA GCT GAC CAG 1523 Lys Ala Leu Gly Glu Arg Ile Phe Ala Leu Glu Ala Thr Ala Asp Gin 325 330 335 340

TCA GCA GCT TCA TTT GAG ATG GAA ATG TCT CAG ACT GGC TTC AGT GCT 1571 Ser Ala Ala Ser Phe Glu Met Glu Met Ser Gin Thr Gly Phe Ser Ala 345 350 355

CAC TAC TCC CAG GAC TGG GTC ATG CTT GGA GCG GTG GGA GCC TAT GAC 1619 His Tyr Ser Gin Asp Trp Val Met Leu Gly Ala Val Gly Ala Tyr Asp 360 365 370

TGG AAC GGA ACT GTG GTC ATG CAG AAG GCT AAC CAG ATG GTC ATC CCT 1667 Trp Asn Gly Thr Val Val Met Gin Lys Ala Asn Gin Met Val Ile Pro 375 380 385

CAT AAC ACC ACC TTT CAA ACT GAG CCC GCC AAG ATG AAC GAG CCT CTG 1715 His Asn Thr Thr Phe Gin Thr Glu Pro Ala Lys Met Asn Glu Pro Leu 390 395 400

GCT TCT TAT TTA GGT TAC ACA GTG AAC TCG GCC ACC ATC CCT GGA GAT 1763 Ala Ser Tyr Leu Gly Tyr Thr Val Asn Ser Ala Thr Ile Pro Gly Asp 405 410 415 420

GTG CTC TAC ATC GCT GGG CAG CCT CGG TAC AAT CAT ACG GGC CAG GTC 1811 Val Leu Tyr Ile Ala Gly Gin Pro Arg Tyr Asn His Thr Gly Gin Val 425 430 435

GTC ATC TAC AAG ATG GAG GAT GGG AAC ATC AAC ATT CTG CAG ACA CTC 1859 Val Ile Tyr Lys Met Glu Asp Gly Asn Ile Asn Ile Leu Gin Thr Leu 440 445 450

GGC GGA GAG CAG ATT GGT TCC TAC TTT GGT AGT GTC TTA ACA ACA ATT 1907 Gly Gly Glu Gin Ile Gly Ser Tyr Phe Gly Ser Val Leu Thr Thr Ile 455 460 465

GAC ATC GAC AAA GAT TCT TAT ACT GAT CTG CTT CTC GTC GGG GCC CCC 1955 Asp Ile Asp Lys Asp Ser Tyr Thr Asp Leu Leu Leu Val Gly Ala Pro 470 475 480

ATG TAC ATG GGG ACA GAG AAA GAG GAA CAG GGC AAG GTG TAC GTG TAC 2003 Met Tyr Met Gly Thr Glu Lys Glu Glu Gin Gly Lys Val Tyr Val Tyr 485 490 495 500

GCT GTG AAT CAG ACA AGG TTT GAA TAT CAA ATG AGC CTG GAA CCA ATT 2051 Ala Val Asn Gin Thr Arg Phe Glu Tyr Gin Met Ser Leu Glu Pro Ile 505 510 515 GGC AGA CCT GCT GCT CAT CCC TGA AGG ATA ATT CAT GCA CGA AAG AAA 2099 Arg Gin Thr Cys Cys Ser Ser Leu Lys Asp Asn Ser Cys Thr Lys Glu 520 525 530

AAC AAG AAT GAG CCC TGC GGG GCC CGC TTC GGA ACA GCA ATT GCT GCT 2147 Asn Lys Asn Glu Pro Cys Gly Ala Arg Phe Gly Thr Ala Ile Ala Ala 535 540 545

GTA AAA GAC CTC AAC GTG GAT GGA TTT AAT GAC GTC GTG ATT GGA GCT 2195 Val Lys Asp Leu Asn Val Asp Gly Phe Asn Asp Val Val Ile Gly Ala 550 555 560

CCG CTG GAA GAT GAC CAC GCA GGA GCT GTG TAC ATT TAT CAT GGC AGT 2243 Pro Leu Glu Asp Asp His Ala Gly Ala Val Tyr Ile Tyr His Gly Ser 565 570 575 580

GGC AAG ACC ATA AGG GAG GCG TAT GCA CAA CGC ATT CCA TCA GGT GGG 2291 Gly Lys Thr Ile Arg Glu Ala Tyr Ala Gin Arg Ile Pro Ser Gly Gly 585 590 595

GAT GGC AAG ACC CTG AAA TTT TTC GGC CAG TCT ATC CAC GGA GAG ATG 2339 Asp Gly Lys Thr Leu Lys Phe Phe Gly Gin Ser Ile His Gly Glu Met 600 605 610

GAT TTA AAT GGT GAC GGT CTG ACT GAC GTG ACC ATT GGA GGC CTT GGT 2387 Asp Leu Asn Gly Asp Gly Leu Thr Asp Val Thr Ile Gly Gly Leu Gly 615 620 625

GGA GCA GCC CTC TTC TGG GCC AGA GAT GTG GCT GTA GTT AAA GTG ACC 2435 Gly Ala Ala Leu Phe Trp Ala Arg Asp Val Ala Val Val Lys Val Thr 630 635 640

ATG AAT TTT GAA CCC AAT AAA GTG AAT ATT CAA AAG AAA AAC TGC CGT 2483 Met Asn Phe Glu Pro Asn Lys Val Asn Ile Gin Lys Lys Asn Cys Arg 645 650 655 660

GTG GAG GGC AAA GAA ACA GTG TGC ATA AAT GCT ACA ATG TGT TTT CAT 2531 Val Glu Gly Lys Glu Thr Val Cys Ile Asn Ala Thr Met Cys Phe His 665 670 675

GTG AAA TTA AAG TCT AAA GAG GAC TCA ATT TAC GAG GCT GAT CTG CAG 2579 Val Lys Leu Lys Ser Lys Glu Asp Ser Ile Tyr Glu Ala Asp Leu Gin 680 685 690

TAC CGT GTC ACC CTT GAT TCA CTG AGG CAG ATA TCA CGG AGC TTT TTT 2627 Tyr Arg Val Thr Leu Asp Ser Leu Arg Gin Ile Ser Arg Ser Phe Phe 695 700 705

TCT GGA ACT CAG GAA AGG AAG ATT CAA AGA AAT ATC ACC GTT CGA GAA 2675 Ser Gly Thr Gin Glu Arg Lys Ile Gin Arg Asn Ile Thr Val Arg Glu 710 715 720

TCA GAA TGC ATC AGG CAC TCC TTC TAC ATG TTG GAC AAA CAT GAC TTT 2723 Ser Glu Cys Ile Arg His Ser Phe Tyr Met Leu Asp Lys His Asp Phe 725 730 735 740 CAG GAC TCT GTG AGA GTG ACT CTG GAT TTT AAT CTC ACT GAT CCA GAA 2771 Gin Asp Ser Val Arg Val Thr Leu Asp Phe Asn Leu Thr Asp Pro Glu 745 750 755

AAT GGT CCT GTA CTT GAT GAC GCT CTG CCA AAC TCA GTC CAC GAA CAC 2819 Asn Gly Pro Val Leu Asp Asp Ala Leu Pro Asn Ser Val His Glu His 760 765 770

ATT CCC TTT GCC AAA GAC TGT GGA AAC AAG GAA AGA TGC ATT TCA GAC 2867 Ile Pro Phe Ala Lys Asp Cys Gly Asn Lys Glu Arg Cys Ile Ser Asp 775 780 785

CTC ACT CTG AAT GTG TCC ACC ACA GAA AAG AGC CTG CTG ATC GTC AAG 2915 Leu Thr Leu Asn Val Ser Thr Thr Glu Lys Ser Leu Leu Ile Val Lys 790 795 800

TCC CAG CAT GAC AAG TTC AAC GTT AGC CTC ACC GTC AAA AAC AAA GGA 2963 Ser Gin His Asp Lys Phe Asn Val Ser Leu Thr Val Lys Asn Lys Gly 805 810 815 820

GAC AGT GCG TAC AAC ACC AGG ACA GTG GTG CAG CAT TCA CCA AAT CTG 3011 Asp Ser Ala Tyr Asn Thr Arg Thr Val Val Gin His Ser Pro Asn Leu 825 830 835

ATT TTT TCG GGA ATT GAG GAG ATC CAA AAA GAT AGC TGT GAA TCT AAT 3059 Ile Phe Ser Gly Ile Glu Glu Ile Gin Lys Asp Ser Cys Glu Ser Asn 840 845 850

CAA AAT ATC ACT TGC AGA GTT GGA TAT CCT TTC CTA AGA GCA GGA GAA 3107 Gin Asn Ile Thr Cys Arg Val Gly Tyr Pro Phe Leu Arg Ala Gly Glu 855 860 865

ACG GTT ACC TTC AAA ATA ATA TTC CAG TTT AAC ACA TCC CAT CTC TCG 3155 Thr Val Thr Phe Lys Ile Ile Phe Gin Phe Asn Thr Ser His Leu Ser 870 875 880

GAA AAT GCA ATC ATT CAC TTA AGT GCA ACA AGT GAC AGT GAG GAG CCC 3203 Glu Asn Ala Ile Ile His Leu Ser Ala Thr Ser Asp Ser Glu Glu Pro 885 890 895 900

CTG GAA TCT CTT AAT GAT AAT GAA GTA AAT ATT TCC ATC CCA GTA AAA 3251 Leu Glu Ser Leu Asn Asp Asn Glu Val Asn Ile Ser Ile Pro Val Lys 905 910 915

TAT GAA GTT GGA CTG CAG TTT TAC AGT TCT GCG AGT GAA CAT CAC ATT 3299 Tyr Glu Val Gly Leu Gin Phe Tyr Ser Ser Ala Ser Glu His His Ile 920 925 930

TCA GTC GCT GCC AAT GAG ACG ATC CCT GAG TTT ATT AAC TCC ACT GAG 3347 Ser Val Ala Ala Asn Glu Thr Ile Pro Glu Phe Ile Asn Ser Thr Glu 935 940 945

GAC ATT GGG AAT GAA ATT AAT GTC TTC TAT ACG ATT AGA AAG AGG GGG 3395 Asp Ile Gly Asn Glu Ile Asn Val Phe Tyr Thr Ile Arg Lys Arg Gly 950 955 960 CAT TTC CCA ATG CCA GAA CTT CAG CTG TCA ATT TCA TTC CCC AAT TTG 3443 His Phe Pro Met Pro Glu Leu Gin Leu Ser Ile Ser Phe Pro Asn Leu 965 970 975 980

ACG GCA GAT GGT TAT CCT GTA CTG TAC CCA ATT GGA TGG TCA TCT TCA 3491 Thr Ala Asp Gly Tyr Pro Val Leu Tyr Pro Ile Gly Trp Ser Ser Ser 985 990 995

GAT AAT GTG AAC TGT AGA CCC CGG AGC CTT GAG GAC CCC TTT GGC ATC 3539 Asp Asn Val Asn Cys Arg Pro Arg Ser Leu Glu Asp Pro Phe Gly Ile 1000 1005 1010

AAC TCT GGG AAG AAA ATG ACA ATA TCG AAG TCT GAG GTT CTC AAA AGA 3587 Asn Ser Gly Lys Lys Met Thr Ile Ser Lys Ser Glu Val Leu Lys Arg 1015 1020 1025

GGC ACA ATC CAG GAC TGC AGT AGT ACG TGT GGA GTT GCC ACC ATC ACG 3635 Gly Thr Ile Gin Asp Cys Ser Ser Thr Cys Gly Val Ala Thr Ile Thr 1030 1035 1040

TGT AGC CTC CTT CCT TCC GAC CTG AGT CAA GTG AAT GTC TCG CTC CTC 3683 Cys Ser Leu Leu Pro Ser Asp Leu Ser Gin Val Asn Val Ser Leu Leu 1045 1050 1055 1060

CTG TGG AAA CCG ACT TTC ATA AGA GCA CAT TTT TCC AGC TTA AAC CTT 3731 Leu Trp Lys Pro Thr Phe Ile Arg Ala His Phe Ser Ser Leu Asn Leu 1065 1070 1075

ACT CTA AGA GGA GAA CTT AAG AGT GAA AAT TCA TCG CTG ACT TTA AGT 3779 Thr Leu Arg Gly Glu Leu Lys Ser Glu Asn Ser Ser Leu Thr Leu Ser 1080 1085 1090

AGC AGC AAC CGG AAG CGA GAG CTG GCT ATT CAG ATA TCC AAA GAC GGG 3827 Ser Ser Asn Arg Lys Arg Glu Leu Ala Ile Gin Ile Ser Lys Asp Gly 1095 1100 1105

CTC CCA GGC AGA GTG CCG CTG TGG GTT ATC CTC CTG AGC GCC TTC GCG 3875 Leu Pro Gly Arg Val Pro Leu Trp Val Ile Leu Leu Ser Ala Phe Ala 1110 1115 1120

GGG CTA CTG CTG CTA ATG CTC CTT ATA TTG GCT CTG TGG AAG ATT GGA 3923 Gly Leu Leu Leu Leu Met Leu Leu Ile Leu Ala Leu Trp Lys Ile Gly 1125 1130 1135 1140

TTC TTC AAA AGG CCA CTG AAG AAG AAA ATG GAG AAA TGAAAGGTTT 3969

Phe Phe Lys Arg Pro Leu Lys Lys Lys Met Glu Lys 1145 1150

CATAGAAAAA AAAAAAAAAA 3987 (2) INFORMATION FOR SEQ ID NO:2:

(i) SEQUENCE CHARACTERISTICS:

(A) LENGTH: 1180 amino acids

(B) TYPE: amino acid

(C) STRANDEDNESS: single

(D) TOPOLOGY: linear

(ii) MOLECULE TYPE: protein

(iii) HYPOTHETICAL: NO

(iv) ANTISENSE: NO

(v) FRAGMENT TYPE: N-terminal

(vi) ORIGINAL SOURCE:

(xi) SEQUENCE DESCRIPTION: SEQ ID NO:2:

Met Val Pro Arg Arg Pro Ala Ser Leu Glu Val Thr Val Ala Cys Ile -28 -25 -20 -15

Trp Leu Leu Thr Val Ile Leu Gly Phe Cys Val Ser Phe Asn Val Asp -10 -5 1

Val Lys Asn Ser Met Ser Phe Ser Gly Pro Val Glu Asp Met Phe Gly 5 10 15 20

Tyr Thr Val Gin Gin Tyr Glu Asn Glu Glu Gly Lys Trp Val Leu Ile 25 30 35

Gly Ser Pro Leu Val Gly Gin Pro Lys Ala Arg Thr Gly Asp Val Tyr 40 45 50

Lys Cys Pro Val Gly Arg Glu Arg Ala Met Pro Cys Val Lys Leu Asp 55 60 65

Glu Pro Val Asn Thr Ser Ile Pro Asn Val Thr Glu Ile Lys Glu Asn 70 75 80

Met Thr Phe Gly Ser Thr Leu Val Thr Asn Pro Asn Gly Gly Phe Leu 85 90 95 100

Ala Cys Gly Pro Leu Tyr Ala Tyr Arg Cys Gly His Leu His Tyr Thr 105 110 115

Thr Gly Ile Cys Ser Asp Val Ser Pro Thr Phe Gin Val Val Asn Ser 120 125 130

Phe Ala Pro Val Gin Glu Cys Ser Thr Gin Leu Asp Ile Val Ile Val 135 140 145

Leu Asp Gly Ser Asn Ser Ile Tyr Pro Trp Glu Ser Val Ile Ala Phe 150 155 160

Leu Asn Asp Leu Leu Lys Arg Met Asp Ile Gly Pro Lys Gin Thr Gin 165 170 175 180

Val Gly Ile Val Gin Tyr Gly Glu Asn Val Thr His Glu Phe Asn Leu 185 190 195 Asn Lys Tyr Ser Ser Thr Glu Glu Val Leu Val Ala Ala Asn Lys Ile 200 205 210

Gly Arg Gin Gly Gly Leu Gin Thr Met Thr Ala Leu Gly Ile Asp Thr 215 220 225

Ala Arg Lys Glu Ala Phe Thr Glu Ala Arg Gly Ala Arg Arg Gly Val 230 235 240

Lys Lys Val Met Val Ile Val Thr Asp Gly Glu Ser His Asp Asn Tyr 245 250 255 260

Arg Leu Lys Gin Val Ile Gin Asp Cys Glu Asp Glu Asn Ile Gin Arg 265 270 275

Phe Ser Ile Ala Ile Leu Gly His Tyr Asn Arg Gly Asn Leu Ser Thr 280 285 290

Glu Lys Phe Val Glu Glu Ile Lys Ser Ile Ala Ser Glu Pro Thr Glu 295 300 305

Lys His Phe Phe Asn Val Ser Asp Glu Leu Ala Leu Val Thr Ile Val 310 315 320

Lys Ala Leu Gly Glu Arg Ile Phe Ala Leu Glu Ala Thr Ala Asp Gin 325 330 335 340

Ser Ala Ala Ser Phe Glu Met Glu Met Ser Gin Thr Gly Phe Ser Ala 345 350 355

His Tyr Ser Gin Asp Trp Val Met Leu Gly Ala Val Gly Ala Tyr Asp 360 365 370

Trp Asn Gly Thr Val Val Met Gin Lys Ala Asn Gin Met Val Ile Pro 375 380 385

His Asn Thr Thr Phe Gin Thr Glu Pro Ala Lys Met Asn Glu Pro Leu 390 395 400

Ala Ser Tyr Leu Gly Tyr Thr Val Asn Ser Ala Thr Ile Pro Gly Asp 405 410 415 420

Val Leu Tyr Ile Ala Gly Gin Pro Arg Tyr Asn His Thr Gly Gin Val 425 430 435

Val Ile Tyr Lys Met Glu Asp Gly Asn Ile Asn Ile Leu Gin Thr Leu 440 445 450

Gly Gly Glu Gin Ile Gly Ser Tyr Phe Gly Ser Val Leu Thr Thr Ile 455 460 465

Asp Ile Asp Lys Asp Ser Tyr Thr Asp Leu Leu Leu Val Gly Ala Pro 470 475 480

Met Tyr Met Gly Thr Glu Lys Glu Glu Gin Gly Lys Val Tyr Val Tyr 485 490 495 500 Ala Val Asn Gin Thr Arg Phe Glu Tyr Gin Met Ser Leu Glu Pro Ile 505 510 515

Arg Gin Thr Cys Cys Ser Ser Leu Lys Asp Asn Ser Cys Thr Lys Glu 520 525 530

Asn Lys Asn Glu Pro Cys Gly Ala Arg Phe Gly Thr Ala Ile Ala Ala 535 540 545

Val Lys Asp Leu Asn Val Asp Gly Phe Asn Asp Val Val Ile Gly Ala 550 555 560

Pro Leu Glu Asp Asp His Ala Gly Ala Val Tyr Ile Tyr His Gly Ser 565 570 575 580

Gly Lys Thr Ile Arg Glu Ala Tyr Ala Gin Arg Ile Pro Ser Gly Gly 585 590 595

Asp Gly Lys Thr Leu Lys Phe Phe Gly Gin Ser Ile His Gly Glu Met 600 605 610

Asp Leu Asn Gly Asp Gly Leu Thr Asp Val Thr Ile Gly Gly Leu Gly 615 620 625

Gly Ala Ala Leu Phe Trp Ala Arg Asp Val Ala Val Val Lys Val Thr 630 635 640

Met Asn Phe Glu Pro Asn Lys Val Asn Ile Gin Lys Lys Asn Cys Arg 645 650 655 660

Val Glu Gly Lys Glu Thr Val Cys Ile Asn Ala Thr Met Cys Phe His 665 670 675

Val Lyε Leu Lys Ser Lys Glu Asp Ser Ile Tyr Glu Ala Asp Leu Gin 680 685 690

Tyr Arg Val Thr Leu Asp Ser Leu Arg Gin Ile Ser Arg Ser Phe Phe 695 700 705

Ser Gly Thr Gin Glu Arg Lys Ile Gin Arg Asn Ile Thr Val Arg Glu 710 715 720

Ser Glu Cys Ile Arg His Ser Phe Tyr Met Leu Asp Lys His Asp Phe 725 730 735 740

Gin Asp Ser Val Arg Val Thr Leu Asp Phe Asn Leu Thr Asp Pro Glu 745 750 755

Asn Gly Pro Val Leu Asp Asp Ala Leu Pro Asn Ser Val His Glu His 760 765 770

Ile Pro Phe Ala Lys Asp Cys Gly Asn Lys Glu Arg Cys Ile Ser Asp 775 780 785

Leu Thr Leu Asn Val Ser Thr Thr Glu Lys Ser Leu Leu Ile Val Lys 790 795 800 Ser Gin His Asp Lys Phe Asn Val Ser Leu Thr Val Lys Asn Lys Gly 805 810 815 820

Asp Ser Ala Tyr Asn Thr Arg Thr Val Val Gin His Ser Pro Asn Leu 825 830 835

Ile Phe Ser Gly Ile Glu Glu Ile Gin Lys Asp Ser Cys Glu Ser Asn 840 845 850

Gin Asn Ile Thr Cys Arg Val Gly Tyr Pro Phe Leu Arg Ala Gly Glu 855 860 865

Thr Val Thr Phe Lys Ile Ile Phe Gin Phe Asn Thr Ser His Leu Ser 870 875 880

Glu Asn Ala Ile Ile His Leu Ser Ala Thr Ser Asp Ser Glu Glu Pro 885 890 895 900

Leu Glu Ser Leu Asn Asp Asn Glu Val Asn Ile Ser Ile Pro Val Lys 905 910 915

Tyr Glu Val Gly Leu Gin Phe Tyr Ser Ser Ala Ser Glu His His Ile 920 925 930

Ser Val Ala Ala Asn Glu Thr Ile Pro Glu Phe Ile Asn Ser Thr Glu 935 940 945

Asp Ile Gly Asn Glu Ile Asn Val Phe Tyr Thr Ile Arg Lys Arg Gly 950 955 960

His Phe Pro Met Pro Glu Leu Gin Leu Ser Ile Ser Phe Pro Asn Leu 965 970 975 980

Thr Ala Asp Gly Tyr Pro Val Leu Tyr Pro Ile Gly Trp Ser Ser Ser 985 990 995

Asp Asn Val Asn Cys Arg Pro Arg Ser Leu Glu Asp Pro Phe Gly Ile 1000 1005 1010

Asn Ser Gly Lys Lys Met Thr Ile Ser Lys Ser Glu Val Leu Lys Arg 1015 1020 1025

Gly Thr Ile Gin Asp Cys Ser Ser Thr Cys Gly Val Ala Thr Ile Thr 1030 1035 1040

Cys Ser Leu Leu Pro Ser Asp Leu Ser Gin Val Asn Val Ser Leu Leu 1045 1050 1055 1060

Leu Trp Lys Pro Thr Phe Ile Arg Ala His Phe Ser Ser Leu Asn Leu 1065 1070 1075

Thr Leu Arg Gly Glu Leu Lys Ser Glu Asn Ser Ser Leu Thr Leu Ser 1080 1085 1090

Ser Ser Asn Arg Lys Arg Glu Leu Ala lie Gin Ile Ser Lys Asp Gly 1095 1100 1105 Leu Pro Gly Arg Val Pro Leu Trp Val Ile Leu Leu Ser Ala Phe Ala 1110 1115 1120

Gly Leu Leu Leu Leu Met Leu Leu Ile Leu Ala Leu Trp Lys Ile Gly 1125 1130 1135 1140

Phe Phe Lys Arg Pro Leu Lys Lys Lys Met Glu Lys 1145 1150

(2) INFORMATION FOR SEQ ID NO:3:

(i) SEQUENCE CHARACTERISTICS:

(A) LENGTH: 5373 base pairs

(B) TYPE: nucleic acid

(C) STRANDEDNESS: single

(D) TOPOLOGY: linear

(ii) MOLECULE TYPE: cDNA (iii) HYPOTHETICAL: NO (iv) ANTISENSE: NO (v) FRAGMENT TYPE: (vi) ORIGINAL SOURCE: (ix) FEATURE:

(A) NAME/KEY: Coding Sequence

(B) LOCATION: 49...3591 (D) OTHER INFORMATION:

(A) NAME/KEY: mat_peptide

(B) LOCATION: 136

(D) OTHER INFORMATION:

(xi) SEQUENCE DESCRIPTION: SEQ ID NO:3:

GAATTCCTGC AAACCCAGCG CAACTACGGT CCCCCGGTCA GACCCAGG ATG GGG CCA 57

Met Gly Pro -29

GAA CGG ACA GGG GCC GCG CCG CTG CCG CTG CTG CTG GTG TTA GCG CTC 105 Glu Arg Thr Gly Ala Ala Pro Leu Pro Leu Leu Leu Val Leu Ala Leu -25 -20 -15

AGT CAA GGC ATT TTA AAT TGT TGT TTG GCC TAC AAT GTT GGT CTC CCA 153 Ser Gin Gly Ile Leu Asn Cys Cys Leu Ala Tyr Asn Val Gly Leu Pro -10 -5 1 5

GAA GCA AAA ATA TTT TCC GGT CCT TCA AGT GAA CAG TTT GGG TAT GCA 201 Glu Ala Lys Ile Phe Ser Gly Pro Ser Ser Glu Gin Phe Gly Tyr Ala 10 15 20

GTG CAG CAG TTT ATA AAT CCA AAA GGC AAC TGG TTA CTG GTT GGT TCA 249 Val Gin Gin Phe Ile Asn Pro Lys Gly Asn Trp Leu Leu Val Gly Ser 25 30 35 CCC TGG AGT GGC TTT CCT GAG AAC CGA ATG GGA GAT GTG TAT AAA TGT 297 Pro Trp Ser Gly Phe Pro Glu Asn Arg Met Gly Asp Val Tyr Lys Cys 40 45 50

CCT GTT GAC CTA TCC ACT GCC ACA TGT GAA AAA CTA AAT TTG CAA ACT 345 Pro Val Asp Leu Ser Thr Ala Thr Cys Glu Lys Leu Asn Leu Gin Thr 55 60 65 70

TCA ACA AGC ATT CCA AAT GTT ACT GAG ATG AAA ACC AAC ATG AGC CTC 393 Ser Thr Ser Ile Pro Asn Val Thr Glu Met Lys Thr Asn Met Ser Leu 75 80 85

GGC TTG ATC CTC ACC AGG AAC ATG GGA ACT GGA GGT TTT CTC ACA TGT 441 Gly Leu Ile Leu Thr Arg Asn Met Gly Thr Gly Gly Phe Leu Thr Cys 90 95 100

GGT CCT CTG TGG GCA CAG CAA TGT GGG AAT CAG TAT TAC ACA ACG GGT 489 Gly Pro Leu Trp Ala Gin Gin Cys Gly Asn Gin Tyr Tyr Thr Thr Gly 105 110 115

GTG TGT TCT GAC ATC AGT CCT GAT TTT CAG CTC TCA GCC AGC TTC TCA 537 Val Cys Ser Asp Ile Ser Pro Asp Phe Gin Leu Ser Ala Ser Phe Ser 120 125 130

CCT GCA ACT CAG CCC TGC CCT TCC CTC ATA GAT GTT GTG GTT GTG TGT 585 Pro Ala Thr Gin Pro Cys Pro Ser Leu Ile Asp Val Val Val Val Cys 135 140 145 150

GAT GAA TCA AAT AGT ATT TAT CCT TGG GAT GCA GTA AAG AAT TTT TTG 633 Asp Glu Ser Asn Ser Ile Tyr Pro Trp Asp Ala Val Lys Asn Phe Leu 155 160 165

GAA AAA TTT GTA CAA GGC CTT GAT ATA GGC CCC ACA AAG ACA CAG GTG 681 Glu Lys Phe Val Gin Gly Leu Asp Ile Gly Pro Thr Lys Thr Gin Val 170 - 175 180

GGG TTA ATT CAG TAT GCC AAT AAT CCA AGA GTT GTG TTT AAC TTG AAC 729 Gly Leu Ile Gin Tyr Ala Asn Asn Pro Arg Val Val Phe Asn Leu Asn 185 190 195

ACA TAT AAA ACC AAA GAA GAA ATG ATT GTA GCA ACA TCC CAG ACA TCC 777 Thr Tyr Lys Thr Lys Glu Glu Met Ile Val Ala Thr Ser Gin Thr Ser 200 205 210

CAA TAT GGT GGG GAC CTC ACA AAC ACA TTC GGA GCA ATT CAA TAT GCA 825 Gin Tyr Gly Gly Asp Leu Thr Asn Thr Phe Gly Ala Ile Gin Tyr Ala 215 220 225 230

AGA AAA TAT GCC TAT TCA GCA GCT TCT GGT GGG CGA CGA AGT GCT ACG 873 Arg Lys Tyr Ala Tyr Ser Ala Ala Ser Gly Gly Arg Arg Ser Ala Thr 235 240 245

AAA GTA ATG GTA GTT GTA ACT GAC GGT GAA TCA CAT GAT GGT TCA ATG 921 Lys Val Met Val Val Val Thr Asp Gly Glu Ser His Asp Gly Ser Met 250 255 260 TTG AAA GCT GTG ATT GAT CAA TGC AAC CAT GAC AAT ATA CTG AGG TTT 969 Leu Lys Ala Val Ile Asp Gin Cys Asn His Asp Asn Ile Leu Arg Phe 265 270 275

GGC ATA GCA GTT CTT GGG TAC TTA AAC AGA AAC GCC CTT GAT ACT AAA 1017 Gly Ile Ala Val Leu Gly Tyr Leu Asn Arg Asn Ala Leu Asp Thr Lys 280 285 290

AAT TTA ATA AAA GAA ATA AAA GCG ATC GCT AGT ATT CCA ACA GAA AGA 1065 Asn Leu Ile Lys Glu Ile Lys Ala Ile Ala Ser Ile Pro Thr Glu Arg 295 300 305 310

TAC TTT TTC AAT GTG TCT GAT GAA GCA GCT CTA CTA GAA AAG GCT GGG 1113 Tyr Phe Phe Asn Val Ser Asp Glu Ala Ala Leu Leu Glu Lys Ala Gly 315 320 325

ACA TTA GGA GAA CAA ATT TTC AGC ATT GAA GGT ACT GTT CAA GGA GGA 1161 Thr Leu Gly Glu Gin Ile Phe Ser Ile Glu Gly Thr Val Gin Gly Gly 330 335 340

GAC AAC TTT CAG ATG GAA ATG TCA CAA GTG GGA TTC AGT GCA GAT TAC 1209 Asp Asn Phe Gin Met Glu Met Ser Gin Val Gly Phe Ser Ala Asp Tyr 345 350 355

TCT TCT CAA AAT GAT ATT CTG ATG CTG GGT GCA GTG GGA GCT TTT GGC 1257 Ser Ser Gin Asn Asp Ile Leu Met Leu Gly Ala Val Gly Ala Phe Gly 360 365 370

TGG AGT GGG ACC ATT GTC CAG AAG ACA TCT CAT GGC CAT TTG ATC TTT 1305 Trp Ser Gly Thr Ile Val Gin Lys Thr Ser His Gly His Leu Ile Phe 375 380 385 390

CCT AAA CAA GCC TTT GAC CAA ATT CTG CAG GAC AGA AAT CAC AGT TCA 1353 Pro Lys Gin Ala Phe Asp Gin Ile Leu Gin Asp Arg Asn His Ser Ser 395 400 405

TAT TTA GGT TAC TCT GTG GCT GCA ATT TCT ACT GGA GAA AGC ACT CAC 1401 Tyr Leu Gly Tyr Ser Val Ala Ala Ile Ser Thr Gly Glu Ser Thr His 410 415 420

TTT GTT GCT GGT GCT CCT CGG GCA AAT TAT ACC GGC CAG ATA GTG CTA 1449 Phe Val Ala Gly Ala Pro Arg Ala Asn Tyr Thr Gly Gin Ile Val Leu 425 430 435

TAT AGT GTG AAT GAG AAT GGC AAT ATC ACG GTT ATT CAG GCT CAC CGA 1497 Tyr Ser Val Asn Glu Asn Gly Asn Ile Thr Val Ile Gin Ala His Arg 440 445 450

GGT GAC CAG ATT GGC TCC TAT TTT GGT AGT GTG CTG TGT TCA GTT GAT 1545 Gly Asp Gin Ile Gly Ser Tyr Phe Gly Ser Val Leu Cys Ser Val Asp 455 460 465 470

GTG GAT AAA GAC ACC ATT ACA GAC GTG CTC TTG GTA GGT GCA CCA ATG 1593 Val Asp Lys Asp Thr Ile Thr Asp Val Leu Leu Val Gly Ala Pro Met 475 480 485 TAC ATG AGT GAC CTA AAG AAA GAG GAA GGA AGA GTC TAC CTG TTT ACT 1641 Tyr Met Ser Asp Leu Lys Lys Glu Glu Gly Arg Val Tyr Leu Phe Thr 490 495 500

ATC AAA AAG GGC ATT TTG GGT CAG CAC CAA TTT CTT GAA GGC CCC GAG 1689 Ile Lys Lys Gly Ile Leu Gly Gin His Gin Phe Leu Glu Gly Pro Glu 505 510 515

GGC ATT GAA AAC ACT CGA TTT GGT TCA GCA ATT GCA GCT CTT TCA GAC 1737 Gly Ile Glu Asn Thr Arg Phe Gly Ser Ala Ile Ala Ala Leu Ser Asp 520 525 530

ATC AAC ATG GAT GGC TTT AAT GAT GTG ATT GTT GGT TCA CCA CTA GAA 1785 Ile Asn Met Asp Gly Phe Asn Asp Val Ile Val Gly Ser Pro Leu Glu 535 540 545 550

AAT CAG AAT TCT GGA GCT GTA TAC ATT TAC AAT GGT CAT CAG GGC ACT 1833 Asn Gin Asn Ser Gly Ala Val Tyr Ile Tyr Asn Gly His Gin Gly Thr 555 560 565

ATC CGC ACA AAG TAT TCC CAG AAA ATC TTG GGA TCC GAT GGA GCC TTT 1881 Ile Arg Thr Lys Tyr Ser Gin Lys Ile Leu Gly Ser Asp Gly Ala Phe 570 576 580

AGG AGC CAT CTC CAG TAC TTT GGG AGG TCC TTG GAT GGC TAT GGA GAT 19 9 Arg Ser His Leu Gin Tyr Phe Gly Arg Ser Leu Asp Gly Tyr Gly Asp 585 590 595

TTA AAT GGG GAT TCC ATC ACC GAT GTG TCT ATT GGT GCC TTT GGA CAA 1977 Leu Asn Gly Asp Ser Ile Thr Asp Val Ser Ile Gly Ala Phe Gly Gin 600 605 610

GTG GTT CAA CTC TGG TCA CAA AGT ATT GCT GAT GTA GCT ATA GAA GCT 2025 Val Val Gin Leu Trp Ser Gin Ser Ile Ala Asp Val Ala Ile Glu Ala 615 620 625 630

TCA TTC ACA CCA GAA AAA ATC ACT TTG GTC AAC AAG AAT GCT CAG ATA 2073 Ser Phe Thr Pro Glu Lys Ile Thr Leu Val Asn Lys Asn Ala Gin Ile 635 640 645

ATT CTC AAA CTC TGC TTC AGT GCA AAG TTC AGA CCT ACT AAG CAA AAC 2121 lie Leu Lys Leu Cys Phe Ser Ala Lys Phe Arg Pro Thr Lys Gin Asn 650 655 660

AAT CAA GTG GCC ATT GTA TAT AAC ATC ACA CTT GAT GCA GAT GGA TTT 216 Asn Gin Val Ala Ile Val Tyr Asn Ile Thr Leu Asp Ala Asp Gly Phe 665 670 675

TCA TCC AGA GTA ACC TCC AGG GGG TTA TTT AAA GAA AAC AAT GAA AGG 2217 Ser Ser Arg Val Thr Ser Arg Gly Leu Phe Lys Glu Asn Asn Glu Arg 680 685 690

TGC CTG CAG AAG AAT ATG GTA GTA AAT CAA GCA CAG AGT TGC CCC GAG 2265 Cys Leu Gin Lys Asn Met Val Val Asn Gin Ala Gin Ser Cys Pro Glu 695 700 715 720 CAC ATC ATT TAT ATA CAG GAG CCC TCT GAT GTT GTC AAC TCT TTG GAT 2313 His Ile Ile Tyr Ile Gin Glu Pro Ser Asp Val Val Asn Ser Leu Asp 725 730 735

TTG CGT GTG GAC ATC AGT CTG GAA AAC CCT GGC ACT AGC CCT GCC CTT 2361 Leu Arg Val Asp Ile Ser Leu Glu Asn Pro Gly Thr Ser Pro Ala Leu 740 745 750

GAA GCC TAT TCT GAG ACT GCC AAG GTC TTC AGT ATT CCT TTC CAC AAA 2409 Glu Ala Tyr Ser Glu Thr Ala Lys Val Phe Ser Ile Pro Phe His Lys 755 760 765

GAC TGT GGT GAG GAT GGA CTT TGC ATT TCT GAT CTA GTC CTA GAT GTC 2457 Asp Cys Gly Glu Asp Gly Leu Cys Ile Ser Asp Leu Val Leu Asp Val 760 765 770

CGA CAA ATA CCA GCT GCT CAA GAA CAA CCC TTT ATT GTC AGC AAC CAA 2505 Arg Gin Ile Pro Ala Ala Gin Glu Gin Pro Phe Ile Val Ser Asn Gin 775 780 785 790

AAC AAA AGG TTA ACA TTT TCA GTA ACA CTG AAA AAT AAA AGG GAA AGT 2553 Asn Lys Arg Leu Thr Phe Ser Val Thr Leu Lys Asn Lys Arg Glu Ser 795 800 805

GCA TAC AAC ACT GGA ATT GTT GTT GAT TTT TCA GAA AAC TTG TTT TTT 2601 Ala Tyr Asn Thr Gly Ile Val Val Asp Phe Ser Glu Asn Leu Phe Phe 810 815 820

GCA TCA TTC TCC CTA CCG GTT GAT GGG ACA GAA GTA ACA TGC CAG GTG 2649 Ala Ser Phe Ser Leu Pro Val Asp Gly Thr Glu Val Thr Cys Gin Val 825 830 835

GCT GCA TCT CAG AAG TCT GTT GCC TGC GAT GTA GGC TAC CCT GCT TTA 2697 Ala Ala Ser Gin Lys Ser Val Ala Cys Asp Val Gly Tyr Pro Ala Leu 840 845 850

AAG AGA GAA CAA CAG GTG ACT TTT ACT ATT AAC TTT GAC TTC AAT CTT 2745 Lys Arg Glu Gin Gin Val Thr Phe Thr Ile Asn Phe Asp Phe Asn Leu 855 860 865 870

CAA AAC CTT CAG AAT CAG GCG TCT CTC AGT TTC CAA GCC TTA AGT GAA 2793 Gin Asn Leu Gin Asn Gin Ala Ser Leu Ser Phe Gin Ala Leu Ser Glu 875 880 885

AGC CAA GAA GAA AAC AAG GCT GAT AAT TTG GTC AAC CTC AAA ATT CCT 2841 Ser Gin Glu Glu Asn Lys Ala Asp Asn Leu Val Asn Leu Lys Ile Pro 890 895 900

CTC CTG TAT GAT GCT GAA ATT CAC TTA ACA AGA TCT ACC AAC ATA AAT 2889 Leu Leu Tyr Asp Ala Glu Ile His Leu Thr Arg Ser Thr Asn Ile Asn 905 910 915

TTT TAT GAA ATC TCT TCG GAT GGG AAT GTT CCT TCA ATC GTG CAC AGT 2937 Phe Tyr Glu Ile Ser Ser Asp Gly Asn Val Pro Ser Ile Val His Ser 920 925 930 TTT GAA GAT GTT GGT CCA AAA TTC ATC TTC TCC CTG AAG GTA ACA ACA 2985 Phe Glu Asp Val Gly Pro Lys Phe Ile Phe Ser Leu Lys Val Thr Thr 935 940 945 950

GGA AGT GTT CCA GTA AGC ATG GCA ACT GTA ATC ATC CAC ATC CCT CAG 3033 Gly Ser Val Pro Val Ser Met Ala Thr Val Ile Ile His Ile Pro Gin 955 960 965

TAT ACC AAA GAA AAG AAC CCA CTG ATG TAC CTA ACT GGG GTG CAA ACA 3081 Tyr Thr Lys Glu Lys Asn Pro Leu Met Tyr Leu Thr Gly Val Gin Thr 970 975 980

GAC AAG GCT GGT GAC ATC AGT TGT AAT GCA GAT ATC AAT CCA CTG AAA 3129 Asp Lys Ala Gly Asp Ile Ser Cys Asn Ala Asp Ile Asn Pro Leu Lys 985 990 995

ATA GGA CAA ACA TCT TCT TCT GTA TCT TTC AAA AGT GAA AAT TTC AGG 3177 Ile Gly Gin Thr Ser Ser Ser Val Ser Phe Lys Ser Glu Asn Phe Arg 1000 1005 1010

CAC ACC AAA GAA TTG AAC TGC AGA ACT GCT TCC TGT AGT AAT GTT ACC 3225 His Thr Lys Glu Leu Asn Cys Arg Thr Ala Ser Cys Ser Asn Val Thr 1015 1020 1025 1030

TGC TGG TTG AAA GAC GTT CAC ATG AAA GGA GAA TAC TTT GTT AAT GTG 3273 Cys Trp Leu Lys Asp Val His Met Lys Gly Glu Tyr Phe Val Asn Val 1035 1040 1045

ACT ACC AGA ATT TGG AAC GGG ACT TTC GCA TCA TCA ACG TTC CAG ACA 3321 Thr Thr Arg Ile Trp Asn Gly Thr Phe Ala Ser Ser Thr Phe Gin Thr 1050 1055 1060

GTA CAG CTA ACG GCA GCT GCA GAA ATC AAC ACC TAT AAC CCT GAG ATA 3369 Val Gin Leu Thr Ala Ala Ala Glu Ile Asn Thr Tyr Asn Pro Glu Ile 1065 1070 1075

TAT GTG ATT GAA GAT AAC ACT GTT ACG ATT CCC CTG ATG ATA ATG AAA 3417 Tyr Val Ile Glu Asp Asn Thr Val Thr Ile Pro Leu Met Ile Met Lys 1080 1085 1090

CCT GAT GAG AAA GCC GAA GTA CCA ACA GGA GTT ATA ATA GGA AGT ATA 3465 Pro Asp Glu Lys Ala Glu Val Pro Thr Gly Val Ile Ile Gly Ser Ile 1095 1100 1105 1110

ATT GCT GGA ATC CTT TTG CTG TTA GCT CTG GTT GCA ATT TTA TGG AAG 3513 Ile Ala Gly Ile Leu Leu Leu Leu Ala Leu Val Ala Ile Leu Trp Lys 1115 1120 1125

CTC GGC TTC TTC AAA AGA AAA TAT GAA AAG ATG ACC AAA AAT CCA GAT 3561 Leu Gly Phe Phe Lys Arg Lys Tyr Glu Lys Met Thr Lys Asn Pro Asp 1130 1135 1140

GAG ATT GAT GAG ACC ACA GAG CTC AGT AGC TGAACCAGCA GACCTACCTG CAGT 3615 Glu Ile Asp Glu Thr Thr Glu Leu Ser Ser 1145 1150 GGGAACCGGC AGCATCCCAG CCAGGGTTTG CTGTTTGCGT GCATGGATTT CTTTTTAAAT 3675

CCCATATTTT TTTTATCATG TCGTAGGTAA ACTAACCTGG TATTTTAAGA GAAAACTGCA 3735

GGTCAGTTTG GATGAAGAAA TTGTGGGGGG TGGGGGAGGT GCGGGGGGCA GGTAGGGAAA 3795

TAATAGGGAA AATACCTATT TTATATGATG GGGGAAAAAA AGTAATCTTT AAACTGGCTG 3855

GCCCAGAGTT TACATTCTAA TTTGCATTGT GTCAGAAACA TGAAATGCTT CCAAGCATGA 3915

CAACTTTTAA AGAAAAATAT GATACTCTCA GATTTTAAGG GGGAAAACTG TTCTCTTTAA 3975

AATATTTGTC TTTAAACAGC AACTACAGAA GTGGAAGTGC TTGATATGTA AGTACTTCCA 4035

CTTGTGTATA TTTTAATGAA TATTGATGTT AACAAGAGGG GAAAACAAAA CACAGGTTTT 4095

TTCAATTTAT GCTGCTCATC CAAAGTTGCC ACAGATGATA CTTCCAAGTG ATAATTTTAT 4155

TTATAAACTA GGTAAAATTT GTTGTTGGTT CCTTTTATAC CACGGCTGCC CCTTCCACAC 4215

CCCATCTTGC TCTAATGATC AAAACATGCT TGAATAACTG AGCTTAGAGT ATACCTCCTA 4275

TATGTCCATT TAAGTTAGGA GAGGGGGCGA TATAGAGACT AAGGCACAAA ATTTTGTTTA 4335

AAACTCAGAA TATAACATTT ATGTAAAATC CCATCTGCTA GAAGCCCATC CTGTGCCAGA 4395

GGAAGGAAAA GGAGGAAATT TCCTTTCTCT TTTAGGAGGC ACAACAGTTC TCTTCTAGGA 4455

TTTGTTTGGC TGACTGGCAG TAACCTAGTG AATTTTTGAA AGATGAGTAA TTTCTTTGGC 4515

AACCTTCCTC CTCCCTTACT GAACCACTCT CCCACCTCCT GGTGGTACCA TTATTATAGA 4575

AGCCCTCTAC AGCCTGACTT TCTCTCCAGC GGTCCAAAGT TATCCCCTCC TTTACCCCTC 4635

ATCCAAAGTT CCCACTCCTT CAGGACAGCT GCTGTGCATT AGATATTAGG GGGGAAAGTC 4695

ATCTGTTTAA TTTACACACT TGCATGAATT ACTGTATATA AACTCCTTAA CTTCAGGGAG 4755

CTATTTTCAT TTAGTGCTAA ACAAGTAAGA AAAATAAGCT AGAGTGAATT TCTAAATGTT 4815

GGAATGTTAT GGGATGTAAA CAATGTAAAG TAAAACACTC TCAGGATTTC ACCAGAAGTT 4875

ACAGATGAGG CACTGGAAAC CACCACCAAA TTAGCAGGTG CACCTTCTGT GGCTGTCTTG 4935

TTTCTGAAGT ACTTTTTCTT CCACAAGAGT GAATTTGACC TAGGCAAGTT TGTTCAAAAG 4995

GTAGATCCTG AGATGATTTG GTCAGATTGG GATAAGGCCC AGCAATCTGC ATTTTAACAA 5055

GCACCCCAGT CACTAGGATG CAGATGGACC ACACTTTGAG AAACACCACC CATTTCTACT 5115

TTTTGCACCT TATTTTCTCT GTTCCTGAGC CCCCACATTC TCTAGGAGAA ACTTAGATTA 5175

AAATTCACAG ACACTACATA TCTAAAGCTT TGACAAGTCC TTGACCTCTA TAAACTTCAG 5235

AGTCCTCATT ATAAAATGGG AAGACTGAGC TGGAGTTCAG CAGTGATGCT TTTTAGTTTT 5295

AAAAGTCTAT GATCTGATCT GGACTTCCTA TAATACAAAT ACACAATCCT CCAAGAATTT 5355

GACTTGGAAA AGGAATTC 5373

(2) INFORMATION FOR SEQ ID NO:4:

(i) SEQUENCE CHARACTERISTICS:

(A) LENGTH: 1181 amino acids

(B) TYPE: amino acid

(C) STRANDEDNESS: single

(D) TOPOLOGY: linear

(ii) MOLECULE TYPE: protein (iii) HYPOTHETICAL: NO (iv) ANTISENSE: NO (v) FRAGMENT TYPE: internal (vi) ORIGINAL SOURCE:

(xi) SEQUENCE DESCRIPTION: SEQ ID NO:4:

Met Gly Pro Glu Arg Thr Gly Ala Ala Pro Leu Pro Leu Leu Leu Val -29 -25 -20 -15

Leu Ala Leu Ser Gin Gly Ile Leu Asn Cys Cys Leu Ala Tyr Asn Val -10 -5 1

Gly Leu Pro Glu Ala Lys Ile Phe Ser Gly Pro Ser Ser Glu Gin Phe 5 10 15 Gly Tyr Ala Val Gin Gin Phe Ile Asn Pro Lys Gly Asn Trp Leu Leu 20 25 30 35

Val Gly Ser Pro Trp Ser Gly Phe Pro Glu Asn Arg Met Gly Asp Val 40 45 50

Tyr Lys Cys Pro Val Asp Leu Ser Thr Ala Thr Cys Glu Lys Leu Asn 55 60 65

Leu Gin Thr Ser Thr Ser Ile Pro Asn Val Thr Glu Met Lys Thr Asn 70 75 80

Met Ser Leu Gly Leu Ile Leu Thr Arg Asn Met Gly Thr Gly Gly Phe 85 90 95

Leu Thr Cys Gly Pro Leu Trp Ala Gin Gin Cys Gly Asn Gin Tyr Tyr 100 105 110 115

Thr Thr Gly Val Cys Ser Asp Ile Ser Pro Asp Phe Gin Leu Ser Ala 120 125 130

Ser Phe Ser Pro Ala Thr Gin Pro Cys Pro Ser Leu Ile Asp Val Val 135 140 145

Val Val Cys Asp Glu Ser Asn Ser Ile Tyr Pro Trp Asp Ala Val Lys 150 155 160

Asn Phe Leu Glu Lys Phe Val Gin Gly Leu Asp Ile Gly Pro Thr Lys 165 170 175

Thr Gin Val Gly Leu Ile Gin Tyr Ala Asn Asn Pro Arg Val Val Phe 180 185 190 195

Asn Leu Asn Thr Tyr Lys Thr Lys Glu Glu Met Ile Val Ala Thr Ser 200 205 210

Gin Thr Ser Gin Tyr Gly Gly Asp Leu Thr Asn Thr Phe Gly Ala Ile 215 220 225

Gin Tyr Ala Arg Lys Tyr Ala Tyr Ser Ala Ala Ser Gly Gly Arg Arg 230 235 240

Ser Ala Thr Lys Val Met Val Val Val Thr Asp Gly Glu Ser His Asp 245 250 255

Gly Ser Met Leu Lys Ala Val Ile Asp Gin Cys Asn His Asp Asn Ile 260 265 270 275

Leu Arg Phe Gly Ile Ala Val Leu Gly Tyr Leu Asn Arg Asn Ala Leu 280 285 290

Asp Thr Lys Asn Leu Ile Lys Glu Ile Lys Ala Ile Ala Ser Ile Pro 295 300 305

Thr Glu Arg Tyr Phe Phe Asn Val Ser Asp Glu Ala Ala Leu Leu Glu 310 315 320 Lys Ala Gly Thr Leu Gly Glu Gin Ile Phe Ser Ile Glu Gly Thr Val 325 330 335

Gin Gly Gly Asp Asn Phe Gin Met Glu Met Ser Gin Val Gly Phe Ser 340 345 350 355

Ala Asp Tyr Ser Ser Gin Asn Asp Ile Leu Met Leu Gly Ala Val Gly 360 365 370

Ala Phe Gly Trp Ser Gly Thr Ile Val Gin Lys Thr Ser His Gly His 375 380 385

Leu Ile Phe Pro Lys Gin Ala Phe Asp Gin Ile Leu Gin Asp Arg Asn 390 395 400

His Ser Ser Tyr Leu Gly Tyr Ser Val Ala Ala Ile Ser Thr Gly Glu 405 410 415

Ser Thr His Phe Val Ala Gly Ala Pro Arg Ala Asn Tyr Thr Gly Gin 420 425 430 435

Ile Val Leu Tyr Ser Val Asn Glu Asn Gly Asn Ile Thr Val Ile Gin 440 445 450

Ala His Arg Gly Asp Gin Ile Gly Ser Tyr Phe Gly Ser Val Leu Cys 455 460 465

Ser Val Asp Val Asp Lys Asp Thr Ile Thr Asp Val Leu Leu Val Gly 470 475 480

Ala Pro Met Tyr Met Ser Asp Leu Lys Lys Glu Glu Gly Arg Val Tyr 485 490 495

Leu Phe Thr Ile Lys Lys Gly Ile Leu Gly Gin His Gin Phe Leu Glu 500 505 510 515

Gly Pro Glu Gly Ile Glu Asn Thr Arg Phe Gly Ser Ala Ile Ala Ala 520 525 530

Leu Ser Asp Ile Asn Met Asp Gly Phe Asn Asp Val lie Val Gly Ser 535 540 545

Pro Leu Glu Asn Gin Asn Ser Gly Ala Val Tyr Ile Tyr Asn Gly His 550 555 560

Gin Gly Thr Ile Arg Thr Lys Tyr Ser Gin Lys Ile Leu Gly Ser Asp 565 570 575

Gly Ala Phe Arg Ser His Leu Gin Tyr Phe Gly Arg Ser Leu Asp Gly 580 585 590 595

Tyr Gly Asp Leu Asn Gly Asp Ser Ile Thr Asp Val Ser Ile Gly Ala 600 605 610

Phe Gly Gin Val Val Gin Leu Trp Ser Gin Ser Ile Ala Asp Val Ala 615 620 625 Ile Glu Ala Ser Phe Thr Pro Glu Lys Ile Thr Leu Val Asn Lys Asn 630 635 640

Ala Gin Ile Ile Leu Lys Leu Cys Phe Ser Ala Lys Phe Arg Pro Thr 645 650 655

Lys Gin Asn Asn Gin Val Ala Ile Val Tyr Asn Ile Thr Leu Asp Ala 660 665 670 675

Asp Gly Phe Ser Ser Arg Val Thr Ser Arg Gly Leu Phe Lys Glu Asn 680 685 690

Asn Glu Arg Cys Leu Gin Lys Asn Met Val Val Asn Gin Ala Gin Ser 695 700 705

Cys Pro Glu His Ile Ile Tyr Ile Gin Glu Pro Ser Asp Val Val Asn 710 715 720

Ser Leu Asp Leu Arg Val Asp Ile Ser Leu Glu Asn Pro Gly Thr Ser 725 730 735

Pro Ala Leu Glu Ala Tyr Ser Glu Thr Ala Lys Val Phe Ser Ile Pro 740 745 750 755

Phe His Lys Asp Cys Gly Glu Asp Gly Leu Cys Ile Ser Asp Leu Val 760 765 770

Leu Asp Val Arg Gin Ile Pro Ala Ala Gin Glu Gin Pro Phe Ile Val 775 780 785

Ser Asn Gin Asn Lys Arg Leu Thr Phe Ser Val Thr Leu Lys Asn Lys 790 795 800

Arg Glu Ser Ala Tyr Asn Thr Gly Ile Val Val Asp Phe Ser Glu Asn 805 810 815

Leu Phe Phe Ala Ser Phe Ser Leu Pro Val Asp Gly Thr Glu Val Thr 820 825 830 835

Cys Gin Val Ala Ala Ser Gin Lys Ser Val Ala Cys Asp Val Gly Tyr 840 845 850

Pro Ala Leu Lys Arg Glu Gin Gin Val Thr Phe Thr Ile Asn Phe Asp 855 860 865

Phe Asn Leu Gin Asn Leu Gin Asn Gin Ala Ser Leu Ser Phe Gin Ala 870 875 880

Leu Ser Glu Ser Gin Glu Glu Asn Lys Ala Asp Asn Leu Val Asn Leu 885 890 895

Lys Ile Pro Leu Leu Tyr Asp Ala Glu Ile His Leu Thr Arg Ser Thr 900 905 910 915

Asn Ile Asn Phe Tyr Glu Ile Ser Ser Asp Gly Asn Val Pro Ser Ile 920 925 930 Val His Ser Phe Glu Asp Val Gly Pro Lys Phe Ile Phe Ser Leu Lys 935 940 945

Val Thr Thr Gly Ser Val Pro Val Ser Met Ala Thr Val Ile Ile His 950 955 960

Ile Pro Gin Tyr Thr Lys Glu Lys Asn Pro Leu Met Tyr Leu Thr Gly 965 970 975

Val Gin Thr Asp Lys Ala Gly Asp Ile Ser Cys Asn Ala Asp Ile Asn 980 985 990 995

Pro Leu Lys Ile Gly Gin Thr Ser Ser Ser Val Ser Phe Lys Ser Glu 1000 1005 1010

Asn Phe Arg His Thr Lys Glu Leu Asn Cys Arg Thr Ala Ser Cys Ser 1015 1020 1025

Asn Val Thr Cys Trp Leu Lys Asp Val His Met Lys Gly Glu Tyr Phe 1030 1035 1040

Val Asn Val Thr Thr Arg Ile Trp Asn Gly Thr Phe Ala Ser Ser Thr 1045 1050 1055

Phe Gin Thr Val Gin Leu Thr Ala Ala Ala Glu Ile Asn Thr Tyr Asn 1060 1065 1070 1075

Pro Glu Ile Tyr Val Ile Glu Asp Asn Thr Val Thr Ile Pro Leu Met 1080 1085 1090

Ile Met Lys Pro Asp Glu Lys Ala Glu Val Pro Thr Gly Val Ile Ile 1095 1100 1105

Gly Ser Ile Ile Ala Gly Ile Leu Leu Leu Leu Ala Leu Val Ala Ile 1110 1115 1120

Leu Trp Lys Leu Gly Phe Phe Lys Arg Lys Tyr Glu Lys Met Thr Lys 1125 1130 1135

Asn Pro Asp Glu Ile Asp Glu Thr Thr Glu Leu Ser Ser 1140 1145 1150

(2) INFORMATION FOR SEQ ID NO:5:

(i) SEQUENCE CHARACTERISTICS:

(A) LENGTH: 20 base pairs

(B) TYPE: nucleic acid

(C) STRANDEDNESS: single

(D) TOPOLOGY: linear

(ii) MOLECULE TYPE: cDNA (iii) HYPOTHETICAL: NO (iv) ANTISENSE: NO (v) FRAGMENT TYPE: (vi) ORIGINAL SOURCE:

(xi) SEQUENCE DESCRIPTION: SEQ ID NO:5:

CCAGAGTCAC TCTCACAGAG 20

(2) INFORMATION FOR SEQ ID NO:6:

(i) SEQUENCE CHARACTERISTICS:

(A) LENGTH: 19 base pairs

(B) TYPE: nucleic acid

(C) STRANDEDNESS: single

(D) TOPOLOGY: linear

(ii) MOLECULE TYPE: cDNA (iii) HYPOTHETICAL: NO (iv) ANTISENSE: NO (v) FRAGMENT TYPE: (vi) ORIGINAL SOURCE:

(xi) SEQUENCE DESCRIPTION: SEQ ID NO:6:

CACAGCGTAC ACGTACACC 19

(2) INFORMATION FOR SEQ ID NO:7:

(i) SEQUENCE CHARACTERISTICS:

(A) LENGTH: 19 base pairs

(B) TYPE: nucleic acid

(C) STRANDEDNESS: single

(D) TOPOLOGY: linear

(ii) MOLECULE TYPE: cDNA (iii) HYPOTHETICAL: NO (iv) ANTISENSE: NO (v) FRAGMENT TYPE: (vi) ORIGINAL SOURCE:

(xi) SEQUENCE DESCRIPTION: SEQ ID NO:7:

CACTTATAGA CATCTCCAG 19 (2) INFORMATION FOR SEQ ID NO:8:

(i) SEQUENCE CHARACTERISTICS:

(A) LENGTH: 18 base pairs

(B) TYPE: nucleic acid

(C) STRANDEDNESS: single

(D) TOPOLOGY: linear

(ii) MOLECULE TYPE: cDNA (iii) HYPOTHETICAL: NO (iv) ANTISENSE: NO (v) FRAGMENT TYPE: (vi) ORIGINAL SOURCE:

(xi) SEQUENCE DESCRIPTION: SEQ ID NO:8:

CATCCATGTT GATGTCTG 18

(2) INFORMATION FOR SEQ ID NO:9:

(i) SEQUENCE CHARACTERISTICS:

(A) LENGTH: 18 base pairs

(B) TYPE: nucleic acid

(C) STRANDEDNESS: single

(D) TOPOLOGY: linear

(ii) MOLECULE TYPE: cDNA (iii) HYPOTHETICAL: NO (iv) ANTISENSE: NO (v) FRAGMENT TYPE: (vi) ORIGINAL SOURCE:

(xi) SEQUENCE DESCRIPTION: SEQ ID NO:9:

CATGTGATTC ACCGTCAG 18

(2) INFORMATION FOR SEQ ID NO:10:

(i) SEQUENCE CHARACTERISTICS:

(A) LENGTH: 24 base pairs

(B) TYPE: nucleic acid

(C) STRANDEDNESS: single

(D) TOPOLOGY: linear

(ii) MOLECULE TYPE: cDNA (iii) HYPOTHETICAL: NO (iv) ANTISENSE: NO (v) FRAGMENT TYPE: (vi) ORIGINAL SOURCE:

(xi) SEQUENCE DESCRIPTION: SEQ ID NO:10:

GCATATTGAA TTGCTCCGAA TGTG 24 (2) INFORMATION FOR SEQ ID NO:11:

(i) SEQUENCE CHARACTERISTICS:

(A) LENGTH: 17 base pairs

(B) TYPE: nucleic acid

(C) STRANDEDNESS: single

(D) TOPOLOGY: linear

(ii) MOLECULE TYPE: cDNA (iii) HYPOTHETICAL: NO (iv) ANTISENSE: NO (v) FRAGMENT TYPE: (vi) ORIGINAL SOURCE:

(xi) SEQUENCE DESCRIPTION: SEQ ID NO:11:

GGCGTATGCA CAACGCA 17

(2) INFORMATION FOR SEQ ID NO:12:

(i) SEQUENCE CHARACTERISTICS:

(A) LENGTH: 21 base pairs

(B) TYPE: nucleic acid

(C) STRANDEDNESS: single

(D) TOPOLOGY: linear

(ii) MOLECULE TYPE: cDNA (iii) HYPOTHETICAL: NO (iv) ANTISENSE: NO (v) FRAGMENT TYPE: (vi) ORIGINAL SOURCE:

(xi) SEQUENCE DESCRIPTION: SEQ ID NO:12:

GCGACAGCTG ACCAGTCAGC A 21

(2) INFORMATION FOR SEQ ID NO:13:

(i) SEQUENCE CHARACTERISTICS:

(A) LENGTH: 18 base pairs

(B) TYPE: nucleic acid

(C) STRANDEDNESS: single

(D) TOPOLOGY: linear

(ii) MOLECULE TYPE: cDNA (iii) HYPOTHETICAL: NO (iv) ANTISENSE: NO (v) FRAGMENT TYPE: (vi) ORIGINAL SOURCE:

(xi) SEQUENCE DESCRIPTION: SEQ ID NO:13:

CACTCCTCCA CAGCTCCT 18 (2) INFORMATION FOR SEQ ID NO:14 :

(i) SEQUENCE CHARACTERISTICS:

(A) LENGTH: 15 base pairs

(B) TYPE: nucleic acid

(C) STRANDEDNESS: single

(D) TOPOLOGY: linear

(ii) MOLECULE TYPE: cDNA (iii) HYPOTHETICAL: NO (iv) ANTISENSE: NO (v) FRAGMENT TYPE: (vi) ORIGINAL SOURCE:

(xi) SEQUENCE DESCRIPTION: SEQ ID NO:14:

ACATGTACTC ACTGG 15

(2) INFORMATION FOR SEQ ID NO:15:

(i) SEQUENCE CHARACTERISTICS:

(A) LENGTH: 18 base pairs

(B) TYPE: nucleic acid

(C) STRANDEDNESS: single

(D) TOPOLOGY: linear

(ii) MOLECULE TYPE: cDNA (iii) HYPOTHETICAL: NO (iv) ANTISENSE: NO (v) FRAGMENT TYPE: (vi) ORIGINAL SOURCE:

(xi) SEQUENCE DESCRIPTION: SEQ ID NO:15:

CTCACATGTG GTCCTCTG 18

(2) INFORMATION FOR SEQ ID NO:16:

(i) SEQUENCE CHARACTERISTICS:

(A) LENGTH: 22 base pairs

(B) TYPE: nucleic acid

(C) STRANDEDNESS: single

(D) TOPOLOGY: linear

(ii) MOLECULE TYPE: cDNA (iii) HYPOTHETICAL: NO (iv) ANTISENSE: NO (v) FRAGMENT TYPE: (vi) ORIGINAL SOURCE:

(xi) SEQUENCE DESCRIPTION: SEQ ID NO:16:

GTCCTGTTGA CCTATCCACT GC 22

Claims

WE CLAIM:

1. A method to identify a mammal having or at risk for developing glomemlopathy comprising the steps of: analyzing a tissue sample from a mammal known to contain cells expressing integrin RNA or protein for integrin subunit expression; and comparing integrin subunit expression in the sample with a control tissue sample, wherein altered integrin subunit expression is conelated with glomemlopathy.

2. The method of Claim 1 , wherein the mammal is a human.

3. The method of Claim 1, wherein the tissue sample is a kidney biopsy.

4. The method of Claim 1 , wherein the tissue sample is blood.

5. The method of Claim 4, wherein the blood sample contains polymorphonuclear cells or monocytes.

6. The method of Claim 1, wherein the tissue sample is a skin biopsy.

7. The method of Claim 1, wherein said analysis comprises in situ hybridization.

8. The method of Claim 7, wherein said in situ hybridization comprises PCR enhanced in situ hybridization.

9. The method of Claim 1, wherein said analyzing comprises isolating RNA from the sample.

10. The method of Claim 1, wherein said analyzing comprises performing PCR, detecting amplified fragments from an integrin subunit and comparing the amount of amplified fragments to the amount of amplified fragments obtained from the control.

11. The method of claim 1 , wherein the integrin subunit is an alpha integrin subunit.

12. The method of Claim 11, wherein the α integrin subunit is αl, α2, α3, or α5 integrin subunit.

13. The method of claim 12, wherein the α integrin subunit is α 1 or α2 integrin subunit.

14. The method of claim 1 , wherein a decrease in αl integrin subunit in the tissue sample as compared with control tissue is conelated with nephropathy.

15. The method of claim 1, wherein an increase in α2 α3, α5, or βl integrin subunit in the tissue sample as compared with control tissue is conelated with nephropathy.

16. The method of claim 1 , wherein an increase in α2 and a decrease in α 1 integrin subunit in the tissue sample as compared with control tissue is correlated with nephropathy.

17. The method of Claim 7, wherein a nucleic acid probe is used to detect integrin, and the probe comprises a 3.9kb fragment of αl from the 5' end to nucleotide 3900.

18. The method of Claim 7, wherein a nucleic acid probe is used to detect integrin, and the probe comprises a 1.8kb fragment of α2 from 5' end through the EcoRI site at nucleotide 1800.

19. The method of Claim 1 , wherein said analyzing comprises incubating the sample with an anti-integrin subunit antibody.

20. The method of Claim 1 , wherein the nondiabetic control sample is from a mammal with no history of hypertension.

21. The method of Claim 1 , wherein an increase of about 25% - 100% in the level of α2 integrin subunit expression in the sample tissue as compared with the confrol is correlated with nephropathy.

22. The method of Claim 1 , wherein a decrease of about 25% - 100% in the level of αl integrin subunit expression in the sample tissue as compared with the control is correlated with nephropathy.

23. A method to identify a mammal having or at risk for developing glomemlopathy comprising the steps of: analyzing a tissue sample from a mammal known to contain cells expressing integrin protein for αl and α2 integrin subunit expression as compared with a control tissue sample; and conelating a decreased level of αl integrin subunit expression and/or an increased level of α2 integrin subunit expression in the sample tissue as compared to the control with nephropathy.

24. A method to identify a mammal with diabetes who has or is at risk for developing secondary pathological changes associated with diabetes comprising the steps of: analyzing a tissue sample from a mammal known to contain cells expressing integrin protein for integrin subunit expression; and correlating alterations in the level of expression of least one integrin subunit as compared with a control tissue sample with the presence of or the risk for developing secondary pathological changes associated with diabetes.

25. The method of claim 25, wherein said integrin subunit is αl, α2, α3, α5, or βl .

26. The method of claim 25, wherein said integrin subunit is αl or α2.

27. The method of claim 1 , wherein said comparing of a sample with a control comprises comparing a first sample obtained from an individual with a second sample obtained from the same individual at a later sampling time.

28. A kit for the diagnosis of nephropathy comprising: two sets of hybridization probes or antibodies capable of detecting each of αl and α2 integrin subunit expression in a tissue sample.

29. The kit of claim 28 further comprising primer sets for the amplification of αl and α2 integrin subunits.

30. The kit of claim 28 further comprising control, standard αl and α2 integrin subunits.