Congenital nephrotic syndrome in mice lacking CD2-associated protein.

نویسندگان

  • N Y Shih
  • J Li
  • V Karpitskii
  • A Nguyen
  • M L Dustin
  • O Kanagawa
  • J H Miner
  • A S Shaw
چکیده

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 cell foot processes, accompanied by mesangial cell hyperplasia and extracellular matrix deposition. Supporting a role for CD2AP in the specialized cell junction known as the slit diaphragm, CD2AP associated with nephrin, the primary component of the slit diaphragm.

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The lack of CD2-associated protein (CD2AP) in mice results in severe congenital nephrotic syndrome: Cd2ap−/− mice die of massive proteinuria shortly after birth, and Cd2ap+/− mice present glomerular disease at nine months with a kidney

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عنوان ژورنال:
  • Science

دوره 286 5438  شماره 

صفحات  -

تاریخ انتشار 1999