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

E3连接酶FBXW7抑制棕色脂肪扩张和白色脂肪褐变

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作者: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

Abstract

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 overexpression in fat suppresses energy expenditure and thermogenesis, 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 proteasomal 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 thermogenic fat biology and energy homeostasis and serves as potential therapeutic target for obesity and metabolic diseases.

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