Peter S. Topham, Hiroshi Kawachi, Samir A. Haydar, Sumant Chugh, Theresa A. Addona, Kathryn B. Charron, Lawrence B. Holzman, Michael Shia, Fujio Shimizu, David J. Salant
J Clin Invest.
1999;
104(11):1559–1566
doi:10.1172/JCI7728
This article Copyright © 1999, The American Society for Clinical Investigation
Abstract
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Ab 5-1-6 identifies an antigen on rat podocyte slit-diaphragms and induces severe proteinuria when injected into rats. Nephrin, an Ig-like transmembrane protein that is mutated in congenital nephrotic syndrome of the Finnish type, has been localized to the slit-diaphragm on human podocytes. Here we document that the mAb 5-1-6 antigen is rat nephrin. After incubation of rat glomeruli with this mAb, the antibody/antigen complex was chemically cross-linked, extracted, and immunoprecipitated, prior to Western analysis. By mass spectrometry and 2D gel electrophoresis, we identified several peptides with complete identity to human nephrin. In addition, the 185-kDa protein immunoprecipitated by mAb 5-1-6 from rat glomerular extracts reacts with a rabbit anti-mouse nephrin antibody. Finally, nephrin and the mAb 5-1-6 antigen have identical glomerular localization patterns on immunofluorescence of rat kidney. These results demonstrate that the nephritogenic mAb 5-1-6 identifies the extracellular domain of nephrin, thereby documenting the importance of the slit-diaphragm and its component, nephrin, in the regulation of glomerular permselectivity.J. Clin. Invest. 104:1559–1566 (1999).
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