Adipose tissue aging partially accounts for fat alterations in HIV lipodystrophy

Lipodystrophy is a major disturbance in people living with HIV-1 (PLWH). Several systemic alterations in PLWH are reminiscent of those that occur in aging. It is unknown whether the lipodystrophy in PLWH is the consequence of accelerated aging in adipose tissue. We compared systemic and adipose tiss...

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Detalles Bibliográficos
Autores: Domingo, Pere (Domingo Pedrol), Giralt i Oms, Marta, Gavaldà i Navarro, Aleix, Blasco Roset, Albert, Delgado Anglés, Alejandro, Gallego Escuredo, José Miguel, Gutiérrez, Maria del Mar, Mateo, Maria Gracia, Cereijo Téllez, Rubén, Domingo i Pedrol, Joan Carles, Villarroya i Gombau, Francesc, Villarroya i Terrade, Joan
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2022
País:España
Institución:Universidad de Barcelona
Repositorio:Dipòsit Digital de la UB
OAI Identifier:oai:diposit.ub.edu:2445/219067
Acceso en línea:https://hdl.handle.net/2445/219067
Access Level:acceso abierto
Palabra clave:Síndrome de lipodistròfia associada a VIH
Inflamació
Autofàgia
Teixit adipós
HIV-associated lipodystrophy syndrome
Inflammation
Autophagy
Adipose tissues
Descripción
Sumario:Lipodystrophy is a major disturbance in people living with HIV-1 (PLWH). Several systemic alterations in PLWH are reminiscent of those that occur in aging. It is unknown whether the lipodystrophy in PLWH is the consequence of accelerated aging in adipose tissue. We compared systemic and adipose tissue disturbances in PLWH with those in healthy elderly individuals (~80 year-old). We observed similarly enhanced expression of inflammation-related genes and decreased autophagy in adipose tissues from elderly individuals and PLWH. Indications of repressed adipogenesis and mitochondrial dysfunction were found specifically in PLWH, whereas reduced telomere length and signs of senesce were specific to elderly individuals. We conclude that aging of adipose tissue accounts only partially for the alterations in adipose tissues of PLWH.