Autophagosome biogenesis: From membrane growth to closure

被引:216
作者
Melia, Thomas J. [1 ]
Lystad, Alf H. [2 ,3 ]
Simonsen, Anne [2 ,3 ]
机构
[1] Yale Univ, Sch Med, Dept Cell Biol, New Haven, CT 06510 USA
[2] Univ Oslo, Fac Med, Inst Basic Med Sci, Dept Mol Med,Inst Clin Med, Oslo, Norway
[3] Univ Oslo, Fac Med, Inst Clin Med, Ctr Canc Cell Reprogramming, Oslo, Norway
关键词
ER-EXIT SITES; ENDOPLASMIC-RETICULUM; REGULATES AUTOPHAGY; ULK1; COMPLEX; ATG PROTEINS; EARLY STEPS; PHOSPHATIDYLINOSITOL; 3-PHOSPHATE; DIRECT PHOSPHORYLATION; INHIBITS AUTOPHAGY; PROMOTES AUTOPHAGY;
D O I
10.1083/jcb.202002085
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Autophagosome biogenesis involves de novo formation of a membrane that elongates to sequester cytoplasmic cargo and closes to form a double-membrane vesicle (an autophagosome). This process has remained enigmatic since its initial discovery >50 yr ago, but our understanding of the mechanisms involved in autophagosome biogenesis has increased substantially during the last 20 yr. Several key questions do remain open, however, including, What determines the site of autophagosome nucleation? What is the origin and lipid composition of the autophagosome membrane? How is cargo sequestration regulated under nonselective and selective types of autophagy? This review provides key insight into the core molecular mechanisms underlying autophagosome biogenesis, with a specific emphasis on membrane modeling events, and highlights recent conceptual advances in the field.
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页数:18
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