Cytosolic lipolysis and lipophagy: two sides of the same coin

被引:383
作者
Zechner, Rudolf [1 ,2 ]
Madeo, Frank [1 ,2 ]
Kratky, Dagmar [1 ,3 ]
机构
[1] BioTechMed Graz, Mozartgasse 12, A-8010 Graz, Austria
[2] Karl Franzens Univ Graz, Inst Mol Biosci, Heinrichstr 31, A-8010 Graz, Austria
[3] Med Univ Graz, Inst Mol Biol & Biochem, Neue Stiftingtalstr 6-6, A-8010 Graz, Austria
基金
欧洲研究理事会; 奥地利科学基金会;
关键词
ADIPOSE TRIGLYCERIDE LIPASE; HORMONE-SENSITIVE LIPASE; LYSOSOMAL ACID LIPASE; SWITCH GENE 2; LIPID-STORAGE DISEASE; EPITHELIUM-DERIVED FACTOR; CHANARIN-DORFMAN-SYNDROME; PROLIFERATOR-ACTIVATED RECEPTORS; CHAPERONE-MEDIATED AUTOPHAGY; CANCER-ASSOCIATED CACHEXIA;
D O I
10.1038/nrm.2017.76
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Fatty acids are the most efficient substrates for energy production in vertebrates and are essential components of the lipids that form biological membranes. Synthesis of triacylglycerols from non-esterified free fatty acids (FFAs) combined with triacylglycerol storage represents a highly efficient strategy to stockpile FFAs in cells and prevent FFA-induced lipotoxicity. Although essentially all vertebrate cells have some capacity to store and utilize triacylglycerols, white adipose tissue is by far the largest triacylglycerol depot and is uniquely able to supply FFAs to other tissues. The release of FFAs from triacylglycerols requires their enzymatic hydrolysis by a process called lipolysis. Recent discoveries thoroughly altered and extended our understanding of lipolysis. This Review discusses how cytosolic 'neutral' lipolysis and lipophagy, which utilizes 'acid' lipolysis in lysosomes, degrade cellular triacylglycerols as well as how these pathways communicate, how they affect lipid metabolism and energy homeostasis and how their dysfunction affects the pathogenesis of metabolic diseases. Answers to these questions will likely uncover novel strategies for the treatment of prevalent metabolic diseases.
引用
收藏
页码:671 / 684
页数:14
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