Department of Physiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Curr Biol. 2017 Apr 24;27(8):R318-R326. doi: 10.1016/j.cub.2017.02.061.
Actin cytoskeleton dynamics play vital roles in most forms of intracellular trafficking by promoting the biogenesis and transport of vesicular cargoes. Mounting evidence indicates that actin dynamics and membrane-cytoskeleton scaffolds also have essential roles in macroautophagy, the process by which cellular waste is isolated inside specialized vesicles called autophagosomes for recycling and degradation. Branched actin polymerization is necessary for the biogenesis of autophagosomes from the endoplasmic reticulum (ER) membrane. Actomyosin-based transport is then used to feed the growing phagophore with pre-selected cargoes and debris derived from different membranous organelles inside the cell. Finally, mature autophagosomes detach from the ER membrane by an as yet unknown mechanism, undergo intracellular transport and then fuse with lysosomes, endosomes and multivesicular bodies through mechanisms that involve actin- and microtubule-mediated motility, cytoskeleton-membrane scaffolds and signaling proteins. In this review, we highlight the considerable progress made recently towards understanding the diverse roles of the cytoskeleton in autophagy.
肌动蛋白细胞骨架动力学在大多数形式的细胞内运输中起着至关重要的作用,促进了囊泡货物的生物发生和运输。越来越多的证据表明,肌动蛋白动力学和膜细胞骨架支架在巨自噬中也具有重要作用,巨自噬是一种将细胞废物隔离在称为自噬体的专门囊泡中进行回收和降解的过程。分支肌动蛋白聚合对于自噬体从内质网(ER)膜的生物发生是必要的。然后,肌球蛋白基运输用于用来自细胞内不同膜细胞器的预先选择的货物和碎片喂养不断生长的吞噬体。最后,成熟的自噬体通过一个尚未确定的机制与 ER 膜分离,通过涉及肌动蛋白和微管介导的运动、细胞骨架-膜支架和信号蛋白的机制进行细胞内运输,然后与溶酶体、内体和多泡体融合。在这篇综述中,我们强调了最近在理解细胞骨架在自噬中的多种作用方面取得的相当大的进展。