Endocytosis and autophagy: Shared machinery for degradation

被引:157
作者
Lamb, Christopher A. [1 ]
Dooley, Hannah C. [1 ]
Tooze, Sharon A. [1 ]
机构
[1] Canc Res UK, London Res Inst, London, England
关键词
autophagy; endosome; lysosome; mTORC1; plasma membrane; CLATHRIN-COATED VESICLES; MEMBRANE-FUSION; AMINO-ACIDS; ENDOPLASMIC-RETICULUM; MOLECULAR-MECHANISMS; ENDOSOME MATURATION; PLASMA-MEMBRANE; PHOSPHOLIPASE-D; SMALL GTPASES; PROTEIN;
D O I
10.1002/bies.201200130
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
Two key questions in the autophagy field are the mechanisms that underlie the signals for autophagy initiation and the source of membrane for expansion of the nascent membrane, the phagophore. In this review, we discuss recent findings highlighting the role of the classical endosomal pathway, from plasma membrane to lysosome, in the formation and expansion of the phagophore and subsequent degradation of the autophagosome contents. We also highlight the striking conservation of regulatory factors between the two pathways, including those regulating membrane budding and fusion, and the role of the lysosome in sensing the nutrient status of the cell, regulating mTORC1 activity, and ultimately the initiation of autophagy. Editor's suggested further reading in BioEssays The evolution of dynamin to regulate clathrin-mediated endocytosis Abstract
引用
收藏
页码:34 / 45
页数:12
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