泛素连接酶
产热
白色脂肪组织
泛素
内分泌学
内科学
褐色脂肪组织
生物
基因敲除
脂肪组织
脂滴
细胞生物学
化学
生物化学
医学
基因
细胞凋亡
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,J. Leon Zhao,Yepeng Hu,Minjia Tan
出处
期刊:EMBO Reports
[Springer Nature]
日期:2025-01-02
卷期号:26 (3): 748-767
被引量:2
标识
DOI:10.1038/s44319-024-00337-w
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 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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