AIDS WEEKLY Plus - October 2002Important note: Information in this article was accurate in October 2002. The state of the art may have changed since the publication date.
Click here to return to AIDS WEEKLY PLUS main menu

HIV/AIDS Nephropathy: Mechanisms of virus-induced cell cycle disruption elucidated

AIDSWEEKLY Plus; October 28, 2002
Michael Greer, Senior Medical Writer


NewsRx -- Researchers in the United States have shed new light on the processes that lead to the development of kidney dysfunction in HIV patients.

"The aberrant cell-cycle progression of HIV-1-infected kidney cells plays a major role in the pathogenesis of HIV-associated nephropathy," explained Peter. J. Murphy and colleagues at Mount Sinai School of Medicine in New York City, "however, the mechanisms whereby HIV-1 induces infected glomerular podocytes or infected tubular epithelium to exit quiescence are largely unknown."

Murphy and coauthors found that HIV genes trigger the expression of cyclin D1 and other cell cycle-associated proteins by podocytes.

The researchers examined podocyte cell cultures and transgenic mice infected with HIV. Podocytes that expressed HIV genes in vitro or in vivo showed a significant upregulation of cyclin D1 mRNA and protein, according to the report.

In addition, infected podocytes expressed phospho-pRb (Ser780) at elevated levels, study data showed. This protein has been linked to cyclin D1-induced G1-to-S phase cell cycle progression.

The cyclin-dependent kinase inhibitor flavopiridol prevented both HIV gene transcription and cyclin D1 expression (HIV-1 expression induces cyclin D1 expression and pRb phosphorylation in infected podocytes: Cell-cycle mechanisms contributing to the proliferative phenotype in HIV-associated nephropathy. BioMed Central Microbiology, 2002;2:26).

"HIV-1 expression induces cyclin D1 and phospho-pRb (Ser780) expression in infected podocytes," Nelson and colleagues concluded, "suggesting that HIV-1 activates cyclin D1-dependent cell-cycle mechanisms to promote proliferation of infected renal epithelium."

The corresponding author for this report is Peter J. Nelson, Division of Nephrology, Mount Sinai School of Medicine, 1 Gustave L. Levy Place, Box 1243, New York, NY 10029, USA. E-mail: peter.nelson@mssm.edu.

Key points reported in this study include:

This article was prepared by AIDS Weekly editors from staff and other reports.

021028
AW021016


Copyright © 2002 - Charles Henderson, Publisher. All rights Reserved. Permission to reproduce granted to AEGIS by Charles W. Henderson. Authorization to reproduce for personal use granted granted by C. W. Henderson, Publisher, provided that the fee of US$4.50 per copy, per page is paid directly to the Copyright Clearance Center, 27 Congress Street, Salem, Massachusetts 01970, USA. Published by Charles Henderson, Publisher. Editorial & Publishing Office: P.O. Box 5528, Atlanta, GA 30307-0528 / Telephone: (800) 633-4931; Subscription Office: P.O. Box 830409, Birmingham, AL 35283-0409 / FAX: (205) 995-1588 http://www.newsrx.net

AEGiS is made possible through unrestricted grants from Boehringer Ingelheim, iMetrikus, Inc., the National Library of Medicine, and donations from users like you. Always watch for outdated information. This article first appeared in 2002. This material is designed to support, not replace, the relationship that exists between you and your doctor.

AEGiS presents published material, reprinted with permission and neither endorses nor opposes any material. All information contained on this website, including information relating to health conditions, products, and treatments, is for informational purposes only. It is often presented in summary or aggregate form. It is not meant to be a substitute for the advice provided by your own physician or other medical professionals. Always discuss treatment options with a doctor who specializes in treating HIV.

Copyright © 1980,2002. AEGiS. All materials appearing on AEGiS are protected by copyright as a collective work or compilation under U.S. copyright and other laws and are the property of AEGiS, or the party credited as the provider of the content.