How lipid droplets "TAG" along: Glycerolipid synthetic enzymes and lipid storage

被引:94
|
作者
Wang, Huan [1 ]
Airola, Michael V. [2 ]
Reue, Karen [1 ,3 ]
机构
[1] Univ Calif Los Angeles, David Geffen Sch Med, Dept Human Genet, Los Angeles, CA 90095 USA
[2] SUNY Stony Brook, Dept Biochem & Cell Biol, Stony Brook, NY 11794 USA
[3] Univ Calif Los Angeles, Inst Mol Biol, Los Angeles, CA 90024 USA
关键词
Triacylglycerol synthesis; Acyltransferase; Mouse model; Human disease mutation; PHOSPHATIDIC-ACID PHOSPHATASE; ACTIVATED RECEPTOR-GAMMA; MITOCHONDRIAL GLYCEROL-3-PHOSPHATE ACYLTRANSFERASE-1; COA-DIACYLGLYCEROL ACYLTRANSFERASE; CONGENITAL GENERALIZED LIPODYSTROPHY; INSULIN-STIMULATED PHOSPHORYLATION; GENE-EXPRESSION; ACYL-COA; HEPATIC STEATOSIS; TRIACYLGLYCEROL SYNTHESIS;
D O I
10.1016/j.bbalip.2017.06.010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Triacylglycerols (TAG) serve as the predominant form of energy storage in mammalian cells, and TAG synthesis influences conditions such as obesity, fatty liver, and insulin resistance. In most tissues, the glycerol 3-phosphate pathway enzymes are responsible for TAG synthesis, and the regulation and function of these enzymes is therefore important for metabolic homeostasis. Here we review the sites and regulation of glycerol-3-phosphate acyltransferase (GPAT), acylglycerol-3-phosphate acyltransferase (AGPAT), lipin phosphatidic acid phosphatase (PAP), and diacylglycerol acyltransferase (DGAT) enzyme action. We highlight the critical roles that these enzymes play in human health by reviewing Mendelian disorders that result from mutation in the corresponding genes. We also summarize the valuable insights that genetically engineered mouse models have provided into the cellular and physiological roles of GPATs, AGPATs, lipins and DGATs. Finally, we comment on the status and feasibility of therapeutic approaches Special Issue entitled: Recent Advances in Lipid Droplet Biology edited by Rosalind Coleman and Matthijs Hesselink.
引用
收藏
页码:1131 / 1145
页数:15
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