Getting ready for building: signaling and autophagosome biogenesis

被引:234
作者
Abada, Adi [1 ]
Elazar, Zvulun [1 ]
机构
[1] Weizmann Inst Sci, Dept Biol Chem, IL-76100 Rehovot, Israel
关键词
Atgs; autophagosome biogenesis; autophagy; mTOR; signaling; PHOSPHATIDYLINOSITOL 3-KINASE COMPLEXES; TRANSFER-RNA SYNTHETASE; REGULATES MTOR; RAG GTPASES; AMINO-ACIDS; EARLY STEPS; DIRECT PHOSPHORYLATION; INHIBITS AUTOPHAGY; HOPS COMPLEX; ATG PROTEINS;
D O I
10.15252/embr.201439076
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Autophagy is the main cellular catabolic process responsible for degrading organelles and large protein aggregates. It is initiated by the formation of a unique membrane structure, the phagophore, which engulfs part of the cytoplasm and forms a double-membrane vesicle termed the autophagosome. Fusion of the outer autophagosomal membrane with the lysosome and degradation of the inner membrane contents complete the process. The extent of autophagy must be tightly regulated to avoid destruction of proteins and organelles essential for cell survival. Autophagic activity is thus regulated by external and internal cues, which initiate the formation of well-defined autophagy-related protein complexes that mediate autophagosome formation and selective cargo recruitment into these organelles. Autophagosome formation and the signaling pathways that regulate it have recently attracted substantial attention. In this review, we analyze the different signaling pathways that regulate autophagy and discuss recent progress in our understanding of autophagosome biogenesis.
引用
收藏
页码:839 / 852
页数:14
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