Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/102812
Title: The molecular signature of HIV-1-associated Lipomatosis reveals differential involvement of Brown and Beige/Brite Adipocyte cell lineages
Author: Cereijo Téllez, Rubén
Gallego Escuredo, José Miguel
Moure Ortega, Ricardo
Villarroya i Terrade, Joan
Domingo i Pedrol, Joan Carles
Fontdevila Font, Joan
Martínez Chamorro, Esteban José
Gutiérrez, Maria del Mar
Gracia Mateo, María
Giralt i Oms, Marta
Domingo, Pere
Villarroya i Gombau, Francesc
Keywords: Teixit adipós
VIH (Virus)
Expressió gènica
Inflamació
Adipose tissues
HIV (Viruses)
Gene expression
Inflammation
Issue Date: Aug-2015
Publisher: Public Library of Science (PLoS)
Abstract: Highly active antiretroviral therapy has remarkably improved quality of life of HIV-1-infected patients. However, this treatment has been associated with the so-called lipodystrophic syndrome, which conveys a number of adverse metabolic effects and morphological alterations. Among them, lipoatrophy of subcutaneous fat in certain anatomical areas and hypertrophy of visceral depots are the most common. Less frequently, lipomatous enlargements of subcutaneous fat at distinct anatomic areas occur. Lipomatous adipose tissue in the dorso-cervical area ('buffalo hump') has been associated with a partial white-to-brown phenotype transition and with increased cell proliferation, but, to date, lipomatous enlargements arising in other parts of the body have not been characterized. In order to establish the main molecular events associated with the appearance of lipomatosis in HIV-1 patients, we analyzed biopsies of lipomatous tissue from 'buffalo hump' and from other anatomical areas in patients, in comparison with healthy subcutaneous adipose tissue, using a marker gene expression approach. Both buffalo-hump and non-buffalo-hump lipomatous adipose tissues exhibited similar patterns of non-compromised adipogenesis, unaltered inflammation, non-fibrotic phenotype and proliferative activity. Shorter telomere length, prelamin A accumulation and SA-β-Gal induction, reminiscent of adipocyte senescence, were also common to both types of lipomatous tissues. Buffalo hump biopsies showed expression of marker genes of brown adipose tissue (e.g. UCP1) and, specifically, of 'classical' brown adipocytes (e.g. ZIC1) but not of beige/brite adipocytes. No such brown fat-related gene expression occurred in lipomatous tissues at other anatomical sites. In conclusion, buffalo hump and other subcutaneous adipose tissue enlargements from HIV-1-infected patients share a similar lipomatous character. However, a distorted induction of white-to-'classical brown adipocyte' phenotype appears unique of dorso-cervical lipomatosis. Thus, the insults caused by HIV-1 viral infection and/or antiretroviral therapy leading to lipomatosis are acting in a location- and adipocyte lineage-dependent manner.
Note: Reproducció del document publicat a: http://dx.doi.org/10.1371/journal.pone.0136571
It is part of: PLoS One, 2015, vol. 10, num. 8, p. e0136571
Related resource: http://dx.doi.org/10.1371/journal.pone.0136571
URI: http://hdl.handle.net/2445/102812
ISSN: 1932-6203
Appears in Collections:Articles publicats en revistes (Medicina)
Articles publicats en revistes (Bioquímica i Biomedicina Molecular)

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