1. Academic Validation
  2. FAT10: a novel mediator of Vpr-induced apoptosis in human immunodeficiency virus-associated nephropathy

FAT10: a novel mediator of Vpr-induced apoptosis in human immunodeficiency virus-associated nephropathy

  • J Virol. 2009 Nov;83(22):11983-8. doi: 10.1128/JVI.00034-09.
Alexandra Snyder 1 Zygimantas Alsauskas Pengfei Gong Paul E Rosenstiel Mary E Klotman Paul E Klotman Michael J Ross
Affiliations

Affiliation

  • 1 Mount Sinai School of Medicine, Division of Nephrology, Box 1243, 1 Gustave L Levy Place, New York, New York 10029, USA.
Abstract

Human immunodeficiency virus (HIV)-associated nephropathy is a significant cause of morbidity and mortality in HIV-infected persons. Vpr-induced cell cycle dysregulation and Apoptosis of renal tubular epithelial cells are important components of the pathogenesis of HIV-associated nephropathy (HIVAN). FAT10 is a ubiquitin-like protein that is upregulated in renal tubular epithelial cells in HIVAN. In these studies, we report that Vpr induces increased expression of FAT10 in tubular cells and that inhibition of FAT10 expression prevents Vpr-induced Apoptosis in human and murine tubular cells. Moreover, we found that Vpr interacts with FAT10 and that these proteins colocalize at mitochondria. These studies establish FAT10 as a novel mediator of Vpr-induced cell death.

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