Secretory Pathways Laboratory, London Research Institute, Cancer Research UK, 44 Lincoln's Inn Fields, London WC2A 3PX, UK.
Curr Opin Cell Biol. 2010 Apr;22(2):150-6. doi: 10.1016/j.ceb.2009.11.013. Epub 2009 Dec 24.
During autophagy, autophagosomes or autophagic vesicles (AVs) are formed and enclose portions of cytosol and/or entire organelles. Distinct from any other cellular vesicle, AVs have a double membrane, between which lies a very limited lumen. To obtain this peculiar topology, the early AV, the phagophore or isolation membrane (IM) must be either synthesised de novo or expanded by vesicle fusion. In support of the latter, recent work has implicated several different organelles as potential membrane sources during the initial stages of IM formation and expansion. Once closed, AVs use the microtubule network to meet and fuse with several different endocytic organelles on their way to becoming degradative AVs. Recent studies have shed light on the machinery required for both these early and late events to occur.
在自噬过程中,自噬体或自噬小泡(AVs)形成并包裹细胞质的部分和/或整个细胞器。与任何其他细胞小泡不同,AVs 具有双层膜,两层膜之间有一个非常有限的腔。为了获得这种特殊的拓扑结构,早期的 AV、吞噬体或隔离膜(IM)必须从头合成或通过囊泡融合来扩展。最近的研究支持了后者,最近的研究表明,在 IM 形成和扩展的初始阶段,几种不同的细胞器可能作为潜在的膜源。一旦封闭,AVs 就会利用微管网络与几个不同的内吞细胞器相遇并融合,最终成为降解性的 AVs。最近的研究揭示了发生这些早期和晚期事件所需的机制。