Adipocyte Piezo1 mediates obesogenic adipogenesis through the FGF1/FGFR1 signaling pathway in mice - Université Côte d'Azur Accéder directement au contenu
Article Dans Une Revue Nature Communications Année : 2020

Adipocyte Piezo1 mediates obesogenic adipogenesis through the FGF1/FGFR1 signaling pathway in mice

Shuang Cao
  • Fonction : Auteur
Dahui Li
  • Fonction : Auteur
Sabrina Kurz
  • Fonction : Auteur
Jiong Hu
Jingchen Shao
  • Fonction : Auteur
Ann Atzberger
  • Fonction : Auteur
Changhe Wang
  • Fonction : Auteur
Weijin Zang
  • Fonction : Auteur
Nina Wettschureck
  • Fonction : Auteur

Résumé

White adipose tissue (WAT) expansion in obesity occurs through enlargement of preexisting adipocytes (hypertrophy) and through formation of new adipocytes (adipogenesis). Adipogenesis results in WAT hyperplasia, smaller adipocytes and a metabolically more favourable form of obesity. How obesogenic WAT hyperplasia is induced remains, however, poorly understood. Here, we show that the mechanosensitive cationic channel Piezo1 mediates dietinduced adipogenesis. Mice lacking Piezo1 in mature adipocytes demonstrated defective differentiation of preadipocyte into mature adipocytes when fed a high fat diet (HFD) resulting in larger adipocytes, increased WAT inflammation and reduced insulin sensitivity. Opening of Piezo1 in mature adipocytes causes the release of the adipogenic fibroblast growth factor 1 (FGF1), which induces adipocyte precursor differentiation through activation of the FGF-receptor-1. These data identify a central feedback mechanism by which mature adipocytes control adipogenesis during the development of obesity and suggest Piezo1mediated adipocyte mechano-signalling as a mechanism to modulate obesity and its metabolic consequences.
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Dates et versions

hal-03380628 , version 1 (15-10-2021)

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Shengpeng Wang, Shuang Cao, Malika Arhatte, Dahui Li, Yue Shi, et al.. Adipocyte Piezo1 mediates obesogenic adipogenesis through the FGF1/FGFR1 signaling pathway in mice. Nature Communications, 2020, 11, ⟨10.1038/s41467-020-16026-w⟩. ⟨hal-03380628⟩
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