Congenital nephrotic syndrome in mice lacking CD2-associated protein

Citation
Ny. Shih et al., Congenital nephrotic syndrome in mice lacking CD2-associated protein, SCIENCE, 286(5438), 1999, pp. 312-315
Citations number
14
Categorie Soggetti
Multidisciplinary,Multidisciplinary,Multidisciplinary
Journal title
SCIENCE
ISSN journal
00368075 → ACNP
Volume
286
Issue
5438
Year of publication
1999
Pages
312 - 315
Database
ISI
SICI code
0036-8075(19991008)286:5438<312:CNSIML>2.0.ZU;2-N
Abstract
CD2-associated protein (CD2AP) is an 80-kilodalton protein that is critical for stabilizing contacts between T cells and antigen-presenting cells. In CD2AP-deficient mice, immune function was compromised, but the mice died at 6 to 7 weeks of age from renal failure. In the kidney, CD2AP was expressed primarily in glomerular epithelial cells. Knockout mice exhibited defects in epithelial tell foot processes, accompanied by mesangial cell hyperplasi a and extracellular matrix deposition. Supporting a role for CD2AP in the s pecialized cell junction known as the slit diaphragm, CD2AP associated with nephrin, the primary component of the slit diaphragm.