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E3 ligase FBXW7 suppresses brown fat expansion and browning of white fat

  • Jian Yu
  • , Xuejiang Gu
  • , Yingying Guo
  • , Mingyuan Gao
  • , Shimiao Cheng
  • , Meiyao Meng
  • , Xiangdi Cui
  • , Zhe Zhang
  • , Wenxiu Guo
  • , Dandan Yan
  • , Maozheng Sheng
  • , Linhui Zhai
  • , Jing Ji
  • , Xinhui Ma
  • , Yu Li
  • , Yuxiang Cao
  • , Xia Wu
  • , Jiejie Zhao
  • , Yepeng Hu
  • , Minjia Tan
  • Yan Lu, Lingyan Xu*, Bin Liu*, Cheng Hu*, Xinran Ma*
*此作品的通讯作者

科研成果: 期刊稿件文章同行评审

摘要

Thermogenic fat, including brown and beige fat, dissipates heat via thermogenesis and enhances energy expenditure. Thus, its activation represents a therapeutic strategy to combat obesity. Here, we demonstrate that levels of F-box and WD repeat domain-containing 7 (FBXW7), an E3 ubiquitin protein ligase, negatively correlate with thermogenic fat functionality. FBXW7 over-expression in fat suppresses energy expenditure and thermogen-esis, thus aggravates obesity and metabolic dysfunctions in mice. Conversely, FBXW7 depletion in fat leads to brown fat expansion and browning of white fat, and protects mice from diet induced obesity, hepatic steatosis, and hyperlipidemia. Mechanistically, FBXW7 binds to S6K1 and promotes its ubiquitination and pro-teasomal degradation, which in turn impacts glycolysis and brown preadipocyte proliferation via lactate. Besides, the beneficial metabolic effects of FBXW7 depletion in fat are attenuated by fat-specific knockdown of S6K1 in vivo. In summary, we provide evidence that adipose FBXW7 acts as a major regulator for thermo-genic fat biology and energy homeostasis and serves as potential therapeutic target for obesity and metabolic diseases.

源语言英语
页(从-至)748-767
页数20
期刊EMBO Reports
26
3
DOI
出版状态已出版 - 10 2月 2025

联合国可持续发展目标

此成果有助于实现下列可持续发展目标:

  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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