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PPAR Res. 2009; 2009: 607902.
Published online 2008 December 1. doi: 10.1155/2009/607902.
PMCID: PMC2593159
HIV-1 Infection and the PPARγ-Dependent Control of Adipose Tissue Physiology
Marta Giralt,1, 2 Pere Domingo,3 and Francesc Villarroya1, 2*
1Department of Biochemistry and Molecular Biology and Institute of Biomedicine, University of Barcelona, 08028 Barcelona, Spain
2CIBER Fisiopatología de la Obesidad y Nutrición, Instituto de Salud Carlos III, 08028 Barcelona, Spain
3Department of Internal Medicine, Hospital de la Santa Creu i Sant Pau, 08025 Barcelona, Spain
*Francesc Villarroya: Email: fvillarroya/at/ub.edu
Recommended by Jacqueline Capeau
Received May 5, 2008; Accepted July 23, 2008.
Abstract
PPARγ is a ligand-dependent master transcription factor controlling adipocyte differentiation as well as multiple biological processes taking place in other cells present in adipose tissue depots such as macrophages. Recent research indicates that HIV-1 infection-related events may alter adipose tissue biology through several mechanisms involving PPARγ, ranging from direct effects of HIV-1-encoded proteins on adipocytes to the promotion of a proinflammatory environment that interferes with PPARγ actions. This effect of HIV-1 on adipose tissue cells can occur even in the absence of direct infection of adipocytes, as soluble HIV-1-encoded proteins such as Vpr may enter cells and inhibit PPARγ action. Moreover, repression of PPARγ actions may relieve inhibitory pathways of HIV-1 gene transcription, thus enhancing HIV-1 effects in infected cells. HIV-1 infection-mediated interference of PPARγ-dependent pathways in adipocytes and other cells inside adipose depots such as macrophages is likely to create an altered local environment that, after antiretroviral treatment, leads to lipodystrophy in HIV-1-infected and HAART-treated patients.