| Literature DB >> 30605677 |
Juan Wang1, Jian-Wei Hao1, Xu Wang1, Huiling Guo1, Hui-Hui Sun1, Xiao-Ying Lai1, Li-Ying Liu1, Mingxia Zhu1, Hao-Yan Wang1, Yi-Fan Li1, Li-Yang Yu1, Changchuan Xie1, Hong-Rui Wang1, Wei Mo1, Hai-Meng Zhou2, Shuai Chen3, Guosheng Liang4, Tong-Jin Zhao5.
Abstract
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.Entities:
Keywords: CD36; DHHC4; DHHC5; fatty acid uptake; protein palmitoylation
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Year: 2019 PMID: 30605677 DOI: 10.1016/j.celrep.2018.12.022
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423