Regulation of lipid droplets by autophagy

被引:188
作者
Dong, Hanqing
Czaja, Mark J. [1 ]
机构
[1] Albert Einstein Coll Med, Marion Bessin Liver Res Ctr, Dept Med, Bronx, NY 10461 USA
基金
美国国家卫生研究院;
关键词
HEPATITIS-B-VIRUS; CELL BIOLOGY; PROTEINS; PHOSPHORYLATION; REPLICATION; EXPRESSION; STARVATION; MACHINERY; UBIQUITIN; LIPOLYSIS;
D O I
10.1016/j.tem.2011.02.003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Autophagy is a lysosomal pathway by which intracellular organelles and proteins are degraded to supply the cell with energy and to maintain cellular homeostasis. Recently, lipid droplets (LDs) have been identified as a substrate for macroautophagy. In addition to the classic pathway of lipid metabolism by cytosolic lipases, LDs are sequestered in autophagosomes that fuse with lysosomes for the breakdown of LD components by lysosomal enzymes. The ability of autophagy to respond to changes in nutrient supply allows the cell to alter LD metabolism to meet the cell's energy demands. Pathophysiological changes in autophagic function can alter cellular lipid metabolism and promote disease states. Autophagy therefore represents a new cellular target for abnormalities in lipid metabolism and accumulation.
引用
收藏
页码:234 / 240
页数:7
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