棕榈酰化
CD36
脂肪酸代谢
化学
游离脂肪酸受体
脂肪酸
生物化学
细胞生物学
脂肪酸结合蛋白
生物
受体
多不饱和脂肪酸
基因
酶
半胱氨酸
作者
Juan Wang,Jian-Wei Hao,Xu Wang,Huiling Guo,Hui-Hui Sun,Xiao-Ying Lai,Li-Ying Liu,Mingxia Zhu,Hao-Yan Wang,Yi-Fan Li,Li-Yang Yu,Changchuan Xie,Hongrui Wang,Wei Mo,Hai‐Meng Zhou,Shuai Chen,Guosheng Liang,Tong‐Jin Zhao
出处
期刊:Cell Reports
[Elsevier]
日期:2019-01-01
卷期号:26 (1): 209-221.e5
被引量:123
标识
DOI:10.1016/j.celrep.2018.12.022
摘要
Fatty acid uptake is the first step in fatty acid utilization, but it remains unclear how the process is regulated. Protein palmitoylation is a fatty acyl modification that plays a key regulatory role in protein targeting and trafficking; however, its function in regulating fatty acid metabolism is unknown. Here, we show that two of the Asp-His-His-Cys (DHHC) motif-containing palmitoyl acyltransferases, DHHC4 and DHHC5, regulate fatty acid uptake. DHHC4 and DHHC5 function at different subcellular localizations to control the palmitoylation, plasma membrane localization, and fatty acid uptake activity of the scavenger receptor CD36. Depletion of either DHHC4 or DHHC5 in cells disrupts CD36-dependent fatty acid uptake. Furthermore, both Dhhc4−/− and adipose-specific Dhhc5 knockout mice show decreased fatty acid uptake activity in adipose tissues and develop severe hypothermia upon acute cold exposure. These findings demonstrate a critical role of DHHC4 and DHHC5 in regulating fatty acid uptake.
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