The perilipin family of lipid droplet proteins: Gatekeepers of intracellular lipolysis

被引:414
|
作者
Sztalryd, Carole [1 ,2 ]
Brasaemle, Dawn L. [3 ,4 ]
机构
[1] Univ Maryland, Sch Med, Dept Med, Div Endocrinol, Baltimore, MD 21201 USA
[2] Baltimore Vet Affairs Hlth Care Ctr, Ctr Geriatr Res Educ & Clin, Baltimore, MD USA
[3] Rutgers State Univ, Dept Nutr Sci, New Brunswick, NJ 08901 USA
[4] Rutgers State Univ, Ctr Lipid Res, New Brunswick, NJ 08901 USA
基金
美国国家卫生研究院;
关键词
Perilipin; Lipid droplet; Triacylglycerol; Lipolysis; Adipose triglyceride lipase; Hormone-sensitive lipase; Monoacylglycerol lipase; ABHD5; Autophagy; ADIPOSE TRIGLYCERIDE LIPASE; HORMONE-SENSITIVE LIPASE; DIFFERENTIATION-RELATED PROTEIN; CHAPERONE-MEDIATED AUTOPHAGY; BETA HYDROLASE DOMAIN; FATTY-ACID OXIDATION; KINASE-A; ADIPOCYTE LIPOLYSIS; POSTTRANSLATIONAL REGULATION; STIMULATED LIPOLYSIS;
D O I
10.1016/j.bbalip.2017.07.009
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
Lipid droplets in chordates are decorated by two or more members of the perilipin family of lipid droplet surface proteins. The perilipins sequester lipids by protecting lipid droplets from lipase action. Their relative expression and protective nature is adapted to the balance of lipid storage and utilization in specific cells. Most cells of the body have tiny lipid droplets with perilipins 2 and 3 at the surfaces, whereas specialized fat-storing cells with larger lipid droplets also express perilipins 1, 4, and/or 5. Perilipins 1, 2, and 5 modulate lipolysis by controlling the access of lipases and co-factors of lipases to substrate lipids stored within lipid droplets. Although perilipin 2 is relatively permissive to lipolysis, perilipins 1 and 5 have distinct control mechanisms that are altered by phosphorylation. Here we evaluate recent progress toward understanding functions of the perilipins with a focus on their role in regulating lipolysis and autophagy. This article is part of a Special Issue entitled: Recent Advances in Lipid Droplet Biology edited by Rosalind Coleman and Matthijs Hesselink.
引用
收藏
页码:1221 / 1232
页数:12
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