Expression of nephrin in acquired human glomerular disease

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Background. Nephrin is a recently identified protein. which is synthesized in the podocytes and localized in the slit diaphragm area. Nephrin is a cell adhesion molecule of the immunoglobulin superfamily, and presumably is a part of the zipper-like structure of the slit membrane. As the Mutation of the gene coding nephrin induces congenital nephrotic syndrome of Finnish type, which is a prototype of nephrotic syndrome, it has been suggested that nephrin also plays a role in acquired proteinuric kidney disease. Methods. To address the above issue, the expression of nephrin in acquired human glomerular disease was studied by immunoelectron microscopy employing a polyclonal antibody against nephrin. Four normal human kidneys from nephrectomy specimens and eight kidney biopsy specimens from glomerular disease patients (one minimal change disease, one membranous glomerulonephritis (GN), one membranoprolifcrative GN, four IgA nephropathy, and one lupus nephritis) were studied. Proteinuria of the patients ranged from 448 to 11725 mg/day. Effacement of the foot processes was observed in all patients. Results. The study demonstrated that the number and distribution of gold particles in the glomerular region, where the podocyte foot process was well preserved, were similar to that found in normal kidneys; however, gold particles were almost always absent in regions where the foot processes were effaced. The number of gold particles per foot process interspace was not different between normal controls and GN patients; however, the number of gold particles per defined length (1000 nm) of the glomerular basement membrane underlying the foot processes was significantly reduced in GN patients. Conclusion. Using immunoelectron microscopy, we observed that the expression of nephrin in GN was lower in regions where the foot processes were effaced, and comparable with that of normal controls where the foot process interspaces were preserved. The significance of our observation in the context of proteinuria in acquired GN needs further clarification.
Publisher
OXFORD UNIV PRESS
Issue Date
2002-03
Language
English
Article Type
Article
Keywords

CONGENITAL NEPHROTIC SYNDROME; SLIT DIAPHRAGM; PROTEIN; RAT

Citation

NEPHROLOGY DIALYSIS TRANSPLANTATION, v.17, no.3, pp.478 - 484

ISSN
0931-0509
DOI
10.1093/ndt/17.3.478
URI
http://hdl.handle.net/10203/5616
Appears in Collection
ITM-Journal Papers(저널논문)
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