生物
细胞生物学
生物发生
内体
自噬
膜
脂质双层融合
小泡
高尔基体
细胞内
生物化学
基因
内质网
细胞凋亡
作者
Suresh Kumar,Ruheena Javed,Michal Mudd,Sandeep Pallikkuth,Keith A. Lidke,Ashish Jain,Karthikeyan Tangavelou,Sigurður Guðmundsson,Chunyan Ye,Tor Erik Rusten,Jan Haug Anonsen,Alf Håkon Lystad,Aurore Claude‐Taupin,Anne Simonsen,Michelle Salemi,Brett S. Phinney,Jing Li,Lian‐Wang Guo,Steven B. Bradfute,Graham S. Timmins,Eeva‐Liisa Eskelinen,Vojo Deretić
出处
期刊:Cell
[Elsevier]
日期:2021-11-01
卷期号:184 (24): 5950-5969.e22
被引量:72
标识
DOI:10.1016/j.cell.2021.10.017
摘要
The biogenesis of mammalian autophagosomes remains to be fully defined. Here, we used cellular and in vitro membrane fusion analyses to show that autophagosomes are formed from a hitherto unappreciated hybrid membrane compartment. The autophagic precursors emerge through fusion of FIP200 vesicles, derived from the cis-Golgi, with endosomally derived ATG16L1 membranes to generate a hybrid pre-autophagosomal structure, HyPAS. A previously unrecognized apparatus defined here controls HyPAS biogenesis and mammalian autophagosomal precursor membranes. HyPAS can be modulated by pharmacological agents whereas its formation is inhibited upon severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection or by expression of SARS-CoV-2 nsp6. These findings reveal the origin of mammalian autophagosomal membranes, which emerge via convergence of secretory and endosomal pathways, and show that this process is targeted by microbial factors such as coronaviral membrane-modulating proteins.
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