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长链脂肪酸的细胞摄取、代谢与感知

Cellular Uptake, Metabolism and Sensing of Long-Chain Fatty Acids.

作者信息

He Qiburi, Chen Yuhao, Wang Zhigang, He Hu, Yu Peng

机构信息

China International Science and Technology Cooperation Base of Food Nutrition/Safety and Medicinal Chemistry, College of Bioengineering, Tianjin University of Science & Technology, 300457 Tianjin, China.

Inner Mongolia Academy of Agricultural & Animal Husbandry Science, 010031 Hohhot, Inner Mongolia, China.

出版信息

Front Biosci (Landmark Ed). 2023 Jan 16;28(1):10. doi: 10.31083/j.fbl2801010.

Abstract

Fatty acids (FAs) are critical nutrients that regulate an organism's health and development in mammal. Long-chain fatty acids (LCFAs) can be divided into saturated and unsaturated fatty acids, depending on whether the carbon chain contains at least 1 double bond. The fatty acids that are required for humans and animals are obtained primarily from dietary sources, and LCFAs are absorbed from outside of cells in mammals. LCFAs enter cells through several mechanisms, including passive diffusion and protein-mediated translocation across the plasma membrane, the latter in which FA translocase (FAT/CD36), plasma membrane FA-binding protein (FABPpm), FA transport protein (FATP), and caveolin-1 are believed to have important functions. The LCFAs that are taken up by cells bind to FA-binding proteins (FABPs) and are transported to the specific organelles, where they are activated into acyl-CoA to target specific metabolic pathways. LCFA-CoAs can be esterified to phospholipids, triacylglycerol, cholesteryl ester, and other specialized lipids. Non-esterified free fatty acids are preferentially stored as triacylglycerol molecules. The main pathway by which fatty acids are catabolized is β-oxidation, which occurs in mitochondria and peroxisomes. stearoyl-CoA desaturase (SCD)-dependent and Fatty acid desaturases (FADS)-dependent fatty acid desaturation pathways coexist in cells and provide metabolic plasticity. The process of fatty acid elongation occurs by cycling through condensation, reduction, dehydration, and reduction. Extracellular LCFA can be mediated by membrane protein G protein-coupled receptor 40 (GPR40) or G protein-coupled receptor 120 (GPR120) to activate mammalian target of rapamycin complex 1 (mTORC1) signaling, and intracellular LCFA's sensor remains to be determined. The crystal structures of a phosphatidic acid phosphatase and a membrane-bound fatty acid elongase-condensing enzyme and other LCFA-related proteins provide important insights into the mechanism of utilization, increasing our understanding of the cellular uptake, metabolism and sensing of LCFAs.

摘要

脂肪酸(FAs)是调节哺乳动物机体健康和发育的关键营养素。长链脂肪酸(LCFAs)可根据碳链是否含有至少1个双键分为饱和脂肪酸和不饱和脂肪酸。人类和动物所需的脂肪酸主要从饮食中获取,哺乳动物的长链脂肪酸是从细胞外吸收的。长链脂肪酸通过多种机制进入细胞,包括被动扩散以及蛋白质介导的跨质膜转运,后者中脂肪酸转位酶(FAT/CD36)、质膜脂肪酸结合蛋白(FABPpm)、脂肪酸转运蛋白(FATP)和小窝蛋白-1被认为具有重要作用。细胞摄取的长链脂肪酸与脂肪酸结合蛋白(FABPs)结合并被转运到特定细胞器,在那里它们被激活为酰基辅酶A以靶向特定代谢途径。LCFA-CoAs可被酯化形成磷脂、三酰甘油、胆固醇酯和其他特殊脂质。未酯化的游离脂肪酸优先储存为三酰甘油分子。脂肪酸分解代谢的主要途径是β-氧化,发生在线粒体和过氧化物酶体中。硬脂酰辅酶A去饱和酶(SCD)依赖性和脂肪酸去饱和酶(FADS)依赖性脂肪酸去饱和途径在细胞中共存并提供代谢可塑性。脂肪酸延长过程通过缩合、还原、脱水和还原循环发生。细胞外长链脂肪酸可由膜蛋白G蛋白偶联受体40(GPR40)或G蛋白偶联受体120(GPR120)介导,以激活雷帕霉素复合物1(mTORC1)信号通路,而细胞内长链脂肪酸的传感器仍有待确定。磷脂酸磷酸酶、膜结合脂肪酸延长酶-缩合酶和其他与LCFA相关蛋白的晶体结构为利用机制提供了重要见解,增进了我们对长链脂肪酸细胞摄取、代谢和感知的理解。

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