Recent data suggest that the glomerular epithelial cell, or podocyte plays a critical role in the function of the blood filter. More importantly, the pathogenesis of a wide variety of glomerular diseases is thought to be secondary to podocyte dysfunction. Little is known, however, about the function of podocytes in glomerular filtration and disease. The focus of this grant application is on CD2AP, an intracellular molecule that we originally discovered as a component of the immune system. CD2AP, however, is highly expressed in podocytes and CD2AP deficient animals die of nephrotic syndrome. This suggests a critical role for CD2AP in podocyte function. Most data suggest that CD2AP is involved in cytoskeletal regulation and in the process of endocytosis and intracellular trafficking. CD2AP heterozygosity appears to be linked with accumulation of immunoglobulin and immune complexes in the glomerular basement membrane (GBM). Based on this data, our current hypothesis proposes that the kidney filter is permeable to serum proteins and that the role of the podocyte is to transport this protein into the urinary space. We postulate that decreased clearance of proteins within the GBM leads to increased susceptibility to immune mediated damage. To test this hypothesis, we propose four specific aims. In the first, we wish to determine whether the accumulation of protein in the GBM leads to increased susceptibility to renal injury by nephrotoxic antibodies or immune complexes. In the second, we investigate how the podocyte might transfer proteins from the GBM to the urinary space and focus on a receptor for albumin and immunoglobulin expressed in podocytes called the neonatal Fc receptor. Third, we speculate that the handling of large volumes of fluid and protein will require an efficient process for internalization and therefore propose to analyze the process of macropinocytosis in podocytes. Lastly, we propose to determine the role of the CD2AP orthologue, Cin85, in the podocyte by generating a conditional Cin85 deficient mouse. We hope that understanding the function of the podocyte will allow a better understanding of the pathogenesis of glomerular diseases which will hopefully lead to more effective therapies for this important class of debilitating diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK058366-08
Application #
7278273
Study Section
Special Emphasis Panel (ZRG1-RUS-B (11))
Program Officer
Mullins, Christopher V
Project Start
2000-08-15
Project End
2010-07-31
Budget Start
2007-08-01
Budget End
2008-07-31
Support Year
8
Fiscal Year
2007
Total Cost
$297,397
Indirect Cost
Name
Washington University
Department
Pathology
Type
Schools of Medicine
DUNS #
068552207
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Funk, Steven D; Lin, Meei-Hua; Miner, Jeffrey H (2018) Alport syndrome and Pierson syndrome: Diseases of the glomerular basement membrane. Matrix Biol 71-72:250-261
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Luo, Wentian; Olaru, Florina; Miner, Jeffrey H et al. (2018) Alternative Pathway Is Essential for Glomerular Complement Activation and Proteinuria in a Mouse Model of Membranous Nephropathy. Front Immunol 9:1433
Brähler, Sebastian; Zinselmeyer, Bernd H; Raju, Saravanan et al. (2018) Opposing Roles of Dendritic Cell Subsets in Experimental GN. J Am Soc Nephrol 29:138-154
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Bartlett, Christina S; Scott, Rizaldy P; Carota, Isabel Anna et al. (2017) Glomerular mesangial cell recruitment and function require the co-receptor neuropilin-1. Am J Physiol Renal Physiol 313:F1232-F1242
Suleiman, Hani Y; Roth, Robyn; Jain, Sanjay et al. (2017) Injury-induced actin cytoskeleton reorganization in podocytes revealed by super-resolution microscopy. JCI Insight 2:
Beckerman, Pazit; Bi-Karchin, Jing; Park, Ae Seo Deok et al. (2017) Transgenic expression of human APOL1 risk variants in podocytes induces kidney disease in mice. Nat Med 23:429-438
Tsuji, Kenji; Suleiman, Hani; Miner, Jeffrey H et al. (2017) Ultrastructural Characterization of the Glomerulopathy in Alport Mice by Helium Ion Scanning Microscopy (HIM). Sci Rep 7:11696

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