To Be or Not to Be? How Selective Autophagy and Cell Death Govern Cell Fate

被引:653
作者
Green, Douglas R. [1 ]
Levine, Beth [2 ,3 ]
机构
[1] St Jude Childrens Res Hosp, Dept Immunol, Memphis, TN 38205 USA
[2] Univ Texas SW Med Ctr Dallas, Ctr Autophagy Res, Dept Internal Med, Dept Microbiol, Dallas, TX 75390 USA
[3] Univ Texas SW Med Ctr Dallas, Howard Hughes Med Inst, Dallas, TX 75390 USA
关键词
PHOSPHATIDYLSERINE EXPOSURE; NONCANONICAL AUTOPHAGY; PATERNAL MITOCHONDRIA; BECLIN; MITOPHAGY; PARKIN; APOPTOSIS; MEMBRANE; ULK1; DEGRADATION;
D O I
10.1016/j.cell.2014.02.049
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
The health of metazoan organisms requires an effective response to organellar and cellular damage either by repair of such damage and/or by elimination of the damaged parts of the cells or the damaged cell in its entirety. Here, we consider the progress that has been made in the last few decades in determining the fates of damaged organelles and damaged cells through discrete, but genetically overlapping, pathways involving the selective autophagy and cell death machinery. We further discuss the ways in which the autophagy machinery may impact the clearance and consequences of dying cells for host physiology. Failure in the proper removal of damaged organelles and/or damaged cells by selective autophagy and cell death processes is likely to contribute to developmental abnormalities, cancer, aging, inflammation, and other diseases.
引用
收藏
页码:65 / 75
页数:11
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