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Article Dans Une Revue Cell Reports Année : 2018

GPS2 Deficiency Triggers Maladaptive White Adipose Tissue Expansion in Obesity via HIF1A Activation

Mano Mathew
Amine Toubal
  • Fonction : Auteur
Fabienne Foufelle

Résumé

Hypertrophic white adipose tissue (WAT) represents a maladaptive mechanism linked to the risk for developing type 2 diabetes in humans. However, the molecular events that predispose WAT to hypertrophy are poorly defined. Here, we demonstrate that adipocyte hypertrophy is triggered by loss of the corepressor GPS2 during obesity. Adipocyte-specific GPS2 deficiency in mice (GPS2 AKO) causes adipocyte hypertrophy, inflammation, and mitochondrial dysfunction during surplus energy. This phenotype is driven by HIF1A activation that orchestrates inadequate WAT remodeling and disrupts mitochondrial activity, which can be reversed by pharmacological or genetic HIF1A inhibition. Correlation analysis of gene expression in human adipose tissue reveals a negative relationship between GPS2 and HIF1A, adipocyte hypertrophy, and insulin resistance. We propose therefore that the obesity-associated loss of GPS2 in adipocytes predisposes for a maladaptive WAT expansion and a pro-diabetic status in mice and humans.

Dates et versions

hal-04014026 , version 1 (03-03-2023)

Identifiants

Citer

Karima Drareni, Raphaëlle Ballaire, Serena Barilla, Mano Mathew, Amine Toubal, et al.. GPS2 Deficiency Triggers Maladaptive White Adipose Tissue Expansion in Obesity via HIF1A Activation. Cell Reports, 2018, 24 (11), pp.2957-2971.e6. ⟨10.1016/j.celrep.2018.08.032⟩. ⟨hal-04014026⟩
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