| Literature DB >> 28559430 |
Shui-Rong Zhou1, Liang Guo1, Xu Wang1, Yang Liu1, Wan-Qiu Peng1, Yuan Liu1, Xiang-Bo Wei1, Xin Dou1, Meng Ding1, Qun-Ying Lei1, Shu-Wen Qian1, Xi Li1, Qi-Qun Tang2.
Abstract
White adipose tissue (WAT) serves as a reversible energy storage depot in the form of lipids in response to nutritional status. Cavin-1, an essential component in the biogenesis of caveolae, is a positive regulator of lipolysis in adipocytes. However, molecular mechanisms of cavin-1 in the modulation of lipolysis remain poorly understood. Here, we showed that cavin-1 was acetylated at lysines 291, 293, and 298 (3K), which were under nutritional regulation in WAT. We further identified GCN5 as the acetyltransferase and Sirt1 as the deacetylase of cavin-1. Acetylation-mimetic 3Q mutants of cavin-1 augmented fat mobilization in 3T3-L1 adipocytes and zebrafish. Mechanistically, acetylated cavin-1 preferentially interacted with hormone-sensitive lipase and recruited it to the caveolae, thereby promoting lipolysis. Our findings shed light on the essential role of cavin-1 in regulating lipolysis in an acetylation-dependent manner in WAT.Entities:
Keywords: HSL; WAT; acetylation; cavin-1; lipolysis
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Year: 2017 PMID: 28559430 PMCID: PMC5533882 DOI: 10.1128/MCB.00058-17
Source DB: PubMed Journal: Mol Cell Biol ISSN: 0270-7306 Impact factor: 4.272