Vesicular trafficking and autophagosome formation

被引:167
作者
Longatti, A. [1 ]
Tooze, S. A. [1 ]
机构
[1] London Res Inst, Secretory Pathways Lab, London WC2A 3PX, England
关键词
autophagy; autophagosome; isolation membrane; phagophore; membrane trafficking; Atg proteins; PHOSPHATIDYLINOSITOL; 3-PHOSPHATE; ENDOPLASMIC-RETICULUM; TUMOR-SUPPRESSOR; PROTEIN-KINASE; REPEAT PROTEIN; BECLIN; MEMBRANE; COMPLEX; INDUCTION; VACUOLE;
D O I
10.1038/cdd.2009.39
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 source of the autophagosome membrane, and the formation of the autophagosome remain the most important questions for understanding autophagy. Fundamentally, the process of autophagosome formation is similar between yeast and mammalian cells and many of the proteins involved (called the autophagy-related (Atg) proteins) are known, having been first discovered in yeast. However, both in yeast and mammalian cells, the molecular details are missing to explain how the double-membrane autophagosome is formed. Important advances in our understanding of the formation process have recently been obtained, and here, we review and interpret these data in the context of well-known paradigms of membrane trafficking to develop some hypothetical models for how an autophagosome forms in mammalian cells. Cell Death and Differentiation (2009) 16, 956-965; doi: 10.1038/cdd.2009.39; published online 17 April 2009
引用
收藏
页码:956 / 965
页数:10
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