Mammalian autophagy: core molecular machinery and signaling regulation

被引:1601
作者
Yang, Zhifen [1 ,2 ]
Klionsky, Daniel J. [1 ,2 ,3 ]
机构
[1] Univ Michigan, Inst Life Sci, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Mol Cellular & Dev Biol, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Dept Biol Chem, Ann Arbor, MI 48109 USA
关键词
BCL-X-L; BECLIN; PHOSPHATIDYLINOSITOL; 3-KINASE; COMPLEX; PROTEIN; PHOSPHORYLATION; CELLS; UVRAG; P53; MACROAUTOPHAGY;
D O I
10.1016/j.ceb.2009.11.014
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Autophagy, a cellular catabolic pathway, is evolutionarily conserved from yeast to mammals. Central to this process is the formation of autophagosomes, double-membrane vesicles responsible for delivering long-lived proteins and excess or damaged organelle into the lysosome for degradation and reuse of the resulting macromolecules. In addition to the hallmark discovery of core molecular machinery components involved in autophagosome formation, complex signaling cascades controlling autophagy have also begun to emerge, with mTOR as a central but far from exclusive player. Malfunction of autophagy has been linked to a wide range of human pathologies, including cancer, neurodegeneration, and pathogen infection. Here we highlight the recent advances in identifying and understanding the core molecular machinery and signaling pathways that are involved in mammalian autophagy.
引用
收藏
页码:124 / 131
页数:8
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