Reggiori Fulvio, Ungermann Christian
Department of Cell Biology, University Medical Center Groningen, University of Groningen, A. Deusinglaan 1, 9713 AV Groningen, The Netherlands.
Department of Biology/Chemistry, University of Osnabrück, Barbarastrasse 13, 49076 Osnabrück, Germany.
J Mol Biol. 2017 Feb 17;429(4):486-496. doi: 10.1016/j.jmb.2017.01.002. Epub 2017 Jan 8.
Macroautophagy, or simply autophagy, is a degradative pathway that delivers cytoplasmic components, including cytosol and organelles, to the lysosome in double-membrane vesicles called autophagosomes. This process is initiated at the pre-autophagosomal structure or phagophore assembly site and involves a number of highly conserved autophagy-related proteins. These support the generation and conversion of an open membranous cistern known as the phagophore or isolation membrane into a closed autophagosome. Within this review, we will focus on recent insights into the molecular events following the sealing/completion of an autophagosome, which lead to its maturation and subsequent fusion with endosomes/lysosomes.
巨自噬,或简称为自噬,是一种降解途径,它将包括细胞质溶胶和细胞器在内的细胞质成分通过称为自噬体的双膜囊泡运送到溶酶体。这个过程在自噬前体结构或吞噬泡组装位点启动,涉及许多高度保守的自噬相关蛋白。这些蛋白支持将称为吞噬泡或隔离膜的开放膜性池生成并转化为封闭的自噬体。在本综述中,我们将重点关注自噬体密封/完成后分子事件的最新见解,这些事件导致其成熟并随后与内体/溶酶体融合。