窖蛋白-2 棕榈酰化周转率通过胰岛素受体酪氨酸激酶促进胰岛素受体底物-1 介导的脂质代谢。

Caveolin-2 palmitoylation turnover facilitates insulin receptor substrate-1-directed lipid metabolism by insulin receptor tyrosine kinase.

机构信息

Division of Life Science, Graduate School of Applied Life Science (BK21 Plus Program), PMBBRC, Gyeongsang National University, Jinju 52828, Republic of Korea.

Department of Anatomy and Convergence Medical Science, College of Medicine, Institute of Medical Sciences, Gyeongsang National University, Jinju 52727, Republic of Korea.

出版信息

Biochim Biophys Acta Mol Basis Dis. 2024 Jun;1870(5):167173. doi: 10.1016/j.bbadis.2024.167173. Epub 2024 Apr 16.

Abstract

Here, we show that insulin induces palmitoylation turnover of Caveolin-2 (Cav-2) in adipocytes. Acyl protein thioesterases-1 (APT1) catalyzes Cav-2 depalmitoylation, and zinc finger DHHC domain-containing protein palmitoyltransferase 21 (ZDHHC21) repalmitoylation of the depalmitoylated Cav-2 for the turnover, thereby controlling insulin receptor (IR)-Cav-2-insulin receptor substrate-1 (IRS-1)-Akt-driven signaling. Insulin-induced palmitoylation turnover of Cav-2 facilitated glucose uptake and fat storage through induction of lipogenic genes. Cav-2-, APT1-, and ZDHHC21-deficient adipocytes, however, showed increased induction of lipolytic genes and glycerol release. In addition, white adipose tissues from insulin sensitive and resistant obese patients exhibited augmented expression of LYPLA1 (APT1) and ZDHHC20 (ZDHHC20). Our study identifies the specific enzymes regulating Cav-2 palmitoylation turnover, and reveals a new mechanism by which insulin-mediated lipid metabolism is controlled in adipocytes.

摘要

在这里,我们表明胰岛素诱导脂肪细胞中窖蛋白-2(Cav-2)的棕榈酰化周转率。酰基蛋白硫酯酶-1(APT1)催化 Cav-2 的去棕榈酰化,锌指 DHHC 结构域含有蛋白棕榈酰转移酶 21(ZDHHC21)对去棕榈酰化的 Cav-2 进行再棕榈酰化以进行周转,从而控制胰岛素受体(IR)-Cav-2-胰岛素受体底物-1(IRS-1)-Akt 驱动的信号转导。胰岛素诱导的 Cav-2 棕榈酰化周转率通过诱导脂肪生成基因促进葡萄糖摄取和脂肪储存。然而,Cav-2、APT1 和 ZDHHC21 缺陷型脂肪细胞中,脂解基因的诱导和甘油释放增加。此外,胰岛素敏感和抵抗肥胖患者的白色脂肪组织中 LYPLA1(APT1)和 ZDHHC20(ZDHHC20)的表达增加。我们的研究确定了调节 Cav-2 棕榈酰化周转率的特定酶,揭示了胰岛素介导的脂肪代谢在脂肪细胞中受到控制的新机制。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索