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

Nat Commun. 2020 May 8;11(1):2303. doi: 10.1038/s41467-020-16026-w.

Abstract

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 diet-induced 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 feed-back mechanism by which mature adipocytes control adipogenesis during the development of obesity and suggest Piezo1-mediated adipocyte mechano-signalling as a mechanism to modulate obesity and its metabolic consequences.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes / metabolism*
  • Adipogenesis / physiology
  • Adipose Tissue, White / metabolism
  • Animals
  • Calorimetry
  • Cells, Cultured
  • Female
  • Fibroblast Growth Factor 1 / genetics
  • Fibroblast Growth Factor 1 / metabolism*
  • Flow Cytometry
  • Humans
  • Immunohistochemistry
  • In Situ Nick-End Labeling
  • Insulin / blood
  • Interleukin-6 / blood
  • Ion Channels / genetics
  • Ion Channels / metabolism*
  • Male
  • Mice
  • Receptor, Fibroblast Growth Factor, Type 1 / genetics
  • Receptor, Fibroblast Growth Factor, Type 1 / metabolism*
  • Signal Transduction / genetics
  • Signal Transduction / physiology

Substances

  • Insulin
  • Interleukin-6
  • Ion Channels
  • Piezo1 protein, mouse
  • Fibroblast Growth Factor 1
  • Receptor, Fibroblast Growth Factor, Type 1