The aim of this project is to study the response of cultured glomerular visceral epithelial cells to nonimmunologic and immunologic injury. Glomerular epithelial cells appear to play a role in puromycin aminonucleoside nephrosis and Heymann nephritis in rat. These experimental models closely resemble human glomerular diseases - minimal change nephrotic syndrome and membranous nephropathy, respectively. We have previously shown that these receptors bear receptors for C3, antigens of Heymann nephritis on their surface and that they synthesize heparan sulfate proteoglycan. Sialic acid residues, richly deposited on these epithelial cells, and, glomerular heparan sulfate are said to be involved in glomerular barrier function against protein loss. Complement system including the membrane attack complex is known to be prominently involved in pathogenesis of many glomerular diseases including Heymann nephritis. Employing the above properties, specifically, we propose to study the following: I. Effect of puromycin aminonucleoside (nonimmunologic injury) on Heymann nephritis related antigen, heparan sulfate and sialic acid contents of glomerular epithelial cells. II. A. Effect of binding of antibody to Heymann nephritis related antigen located on glomerular epithelial cells (immunologic injury) on expression of C3 receptors, content of heparan sulfate and sialic acid. B. Effects of binding of C3 ligands, membrane attack complex, alone or in combination (immunologic injury) on content of heparan sulfate and sialic acid. Methods employed will consist of cell culture of glomerular epithelial cells, quantitative immunoperoxidase, standard rosette techniques using sheep erythrocytes as indicator particles. In immunoperoxidase reactions, highly purified, well described specific antibodies will be used. Standard parametric and nonparametric statistical methods will be used in analysis of results. Our results will advance understanding the role of glomerular visceral epithelial cells in the two experimental renal disease models which are prototypes of common human glomerulopathies.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Unknown (R23)
Project #
1R23DK037517-01
Application #
3447534
Study Section
Cellular Biology and Physiology Subcommittee 1 (CBY)
Project Start
1986-12-01
Project End
1989-11-30
Budget Start
1986-12-01
Budget End
1987-11-30
Support Year
1
Fiscal Year
1987
Total Cost
Indirect Cost
Name
Rush University Medical Center
Department
Type
DUNS #
City
Chicago
State
IL
Country
United States
Zip Code
60612
Singh, A K; Kasinath, B S; Lewis, E J (1992) Interaction of polycations with cell-surface negative charges of epithelial cells. Biochim Biophys Acta 1120:337-42
Kasinath, B S; Singh, A K; Kanwar, Y S et al. (1990) Dexamethasone increases heparan sulfate proteoglycan core protein content of glomerular epithelial cells. J Lab Clin Med 115:196-202
Kasinath, B S; Singh, A K; Kanwar, Y S et al. (1988) Effect of puromycin aminonucleoside on HSPG core protein content of glomerular epithelial cells. Am J Physiol 255:F590-6