Zhou Shui-Rong, Guo Liang, Wang Xu, Liu Yang, Peng Wan-Qiu, Liu Yuan, Wei Xiang-Bo, Dou Xin, Ding Meng, Lei Qun-Ying, Qian Shu-Wen, Li Xi, Tang Qi-Qun
Key Laboratory of Metabolism and Molecular Medicine, Ministry of Education, and Department of Biochemistry and Molecular Biology, Fudan University Shanghai Medical College, Shanghai, People's Republic of China.
Key Laboratory of Metabolism and Molecular Medicine, Ministry of Education, and Department of Biochemistry and Molecular Biology, Fudan University Shanghai Medical College, Shanghai, People's Republic of China
Mol Cell Biol. 2017 Jul 28;37(16). doi: 10.1128/MCB.00058-17. Print 2017 Aug 15.
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.
白色脂肪组织(WAT)作为一种可逆的能量储存库,以脂质形式响应营养状况。小窝蛋白1(Cavin-1)是小窝生物发生的重要组成部分,是脂肪细胞中脂解作用的正向调节因子。然而,Cavin-1在调节脂解作用中的分子机制仍知之甚少。在此,我们发现Cavin-1在赖氨酸291、293和298(3K)处被乙酰化,这些位点在WAT中受营养调节。我们进一步确定GCN5为Cavin-1的乙酰转移酶,Sirt1为其去乙酰化酶。Cavin-1的乙酰化模拟3Q突变体增强了3T3-L1脂肪细胞和斑马鱼中的脂肪动员。机制上,乙酰化的Cavin-1优先与激素敏感性脂肪酶相互作用,并将其招募到小窝,从而促进脂解作用。我们的研究结果揭示了Cavin-1在WAT中以乙酰化依赖方式调节脂解作用中的重要作用。