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

  • Sheng Peng Wang
  • , Shuang Cao
  • , Malika Arhatte
  • , Dahui Li
  • , Yue Shi
  • , Sabrina Kurz
  • , Jiong Hu
  • , Lei Wang
  • , Jingchen Shao
  • , Ann Atzberger
  • , Zheng Wang
  • , Changhe Wang
  • , Weijin Zang
  • , Ingrid Fleming
  • , Nina Wettschureck
  • , Eric Honoré
  • , Stefan Offermanns
  • Max Planck Institute for Heart and Lung Research
  • Xi'an Jiaotong University
  • Université Côte d’Azur
  • The University of Hong Kong
  • Goethe University Frankfurt
  • The First Affiliated Hospital of Xi’an Jiaotong University

科研成果: 期刊稿件文章同行评审

133 引用 (Scopus)

摘要

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.

源语言英语
文章编号2303
期刊Nature Communications
11
1
DOI
出版状态已出版 - 1 12月 2020

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  1. 可持续发展目标 3 - 良好健康与福祉
    可持续发展目标 3 良好健康与福祉

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