UPRES EA4530, Université Paris-Sud, Faculté de Pharmacie, 92296 Châtenay-Malabry, France.
J Cell Sci. 2013 Mar 1;126(Pt 5):1071-80. doi: 10.1242/jcs.115626.
Both at a basal level and after induction (especially in response to nutrient starvation), the function of autophagy is to allow cells to degrade and recycle damaged organelles, proteins and other biological constituents. Here, we focus on the role microtubules have in autophagosome formation, autophagosome transport across the cytoplasm and in the formation of autolysosomes. Recent insights into the exact relationship between autophagy and microtubules now point to the importance of microtubule dynamics, tubulin post-translational modifications and microtubule motors in the autophagy process. Such factors regulate signaling pathways that converge to stimulate autophagosome formation. They also orchestrate the movements of pre-autophagosomal structures and autophagosomes or more globally organize and localize immature and mature autophagosomes and lysosomes. Most of the factors that now appear to link microtubules to autophagosome formation or to autophagosome dynamics and fate were identified initially without the notion that sequestration, recruitment and/or interaction with microtubules contribute to their function. Spatial and temporal coordination of many stages in the life of autophagosomes thus underlines the integrative role of microtubules and progressively reveals hidden parts of the autophagy machinery.
在基础水平和诱导后(特别是在响应营养饥饿时),自噬的功能是允许细胞降解和回收受损的细胞器、蛋白质和其他生物成分。在这里,我们专注于微管在自噬体形成、自噬体穿过细胞质的运输以及自溶体形成中的作用。最近对自噬和微管之间的确切关系的深入了解表明,微管动力学、微管蛋白翻译后修饰和微管马达在自噬过程中非常重要。这些因素调节信号通路,这些信号通路汇聚在一起以刺激自噬体的形成。它们还协调前自噬体结构和自噬体的运动,或者更全面地组织和定位未成熟和成熟的自噬体和溶酶体。现在看来,将微管与自噬体形成或自噬体动力学和命运联系起来的大多数因素最初是在没有认为隔离、募集和/或与微管相互作用有助于其功能的概念的情况下被识别的。自噬体生命的许多阶段的时空协调强调了微管的整合作用,并逐渐揭示了自噬机制的隐藏部分。