Autophagy and signaling: their role in cell survival and cell death

被引:952
|
作者
Codogno, P
Meijer, AJ
机构
[1] INSERM, U504, Inst Andre Lwoff, F-94807 Villejuif, France
[2] Univ Amsterdam, Acad Med Ctr, Dept Med Biochem, NL-1105 AZ Amsterdam, Netherlands
来源
CELL DEATH AND DIFFERENTIATION | 2005年 / 12卷 / Suppl 2期
关键词
amino acids; macroautophagy; signal transduction; mTOR;
D O I
10.1038/sj.cdd.4401751
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
Macroautophagy is a vacuolar, self-digesting mechanism responsible for the removal of long-lived proteins and damaged organelles by the lysosome. The discovery of the ATG genes has provided key information about the formation of the autophagosome, and about the role of macroautophagy in allowing cells to survive during nutrient depletion and/or in the absence of growth factors. Two connected signaling pathways encompassing class-I phosphatidylinositol 3-kinase and (mammalian) target of rapamycin play a central role in controlling macroautophagy in response to starvation. However, a considerable body of literature reports that macroautophagy is also a cell death mechanism that can occur either in the absence of detectable signs of apoptosis (via autophagic cell death) or concomitantly with apoptosis. Macroautophagy is activated by signaling pathways that also control apoptosis. The aim of this review is to discuss the signaling pathways that control macroautophagy during cell survival and cell death.
引用
收藏
页码:1509 / 1518
页数:10
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