Unraveling the roles of PLIN5: linking cell biology to physiology

脂滴包被蛋白 脂滴 生物 细胞生物学 脂肪组织 脂解 细胞 生物化学
作者
Rachael R. Mason,Matthew J. Watt
出处
期刊:Trends in Endocrinology and Metabolism [Elsevier BV]
卷期号:26 (3): 144-152 被引量:82
标识
DOI:10.1016/j.tem.2015.01.005
摘要

•Examination of PLIN5 functions in cultured cells. •Outline of PLIN5 functions uncovered by murine knockout studies in vivo. •Comprehensive analysis of the literature examining PLIN5 in metabolic disease. The discovery of perilipin (PLIN) 1 provided a major conceptual shift in the understanding of adipose tissue lipolysis and generated intense interest in lipid droplet biology research. The subsequent discovery of other PLIN proteins revealed unique tissue distribution profiles, subcellular locations, and lipid-binding properties and divergent cellular functions. PLIN5 is highly expressed in oxidative tissues such as skeletal muscle, liver, and heart and is central to lipid homeostasis in these tissues. Studies in cell systems have ascribed several metabolic roles to PLIN5 and demonstrated interactions with other proteins that are requisite for these functions. We examine recent in vivo studies and ask whether the evidence from the cell biology approaches is consistent with the physiological roles of PLIN5. The discovery of perilipin (PLIN) 1 provided a major conceptual shift in the understanding of adipose tissue lipolysis and generated intense interest in lipid droplet biology research. The subsequent discovery of other PLIN proteins revealed unique tissue distribution profiles, subcellular locations, and lipid-binding properties and divergent cellular functions. PLIN5 is highly expressed in oxidative tissues such as skeletal muscle, liver, and heart and is central to lipid homeostasis in these tissues. Studies in cell systems have ascribed several metabolic roles to PLIN5 and demonstrated interactions with other proteins that are requisite for these functions. We examine recent in vivo studies and ask whether the evidence from the cell biology approaches is consistent with the physiological roles of PLIN5.
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