Xie Zhiping, Klionsky Daniel J
Life Sciences Institute and Department of Molecular, Cellular and Developmental Biology and Biological Chemistry, University of Michigan, Ann Arbor, MI 48109, USA.
Nat Cell Biol. 2007 Oct;9(10):1102-9. doi: 10.1038/ncb1007-1102.
Eukaryotic cells employ autophagy to degrade damaged or obsolete organelles and proteins. Central to this process is the formation of autophagosomes, double-membrane vesicles responsible for delivering cytoplasmic material to lysosomes. In the past decade many autophagy-related genes, ATG, have been identified that are required for selective and/or nonselective autophagic functions. In all types of autophagy, a core molecular machinery has a critical role in forming sequestering vesicles, the autophagosome, which is the hallmark morphological feature of this dynamic process. Additional components allow autophagy to adapt to the changing needs of the cell.
真核细胞利用自噬来降解受损或过时的细胞器和蛋白质。这一过程的核心是自噬体的形成,自噬体是一种双膜囊泡,负责将细胞质物质输送到溶酶体。在过去十年中,许多与自噬相关的基因(ATG)已被鉴定出来,这些基因是选择性和/或非选择性自噬功能所必需的。在所有类型的自噬中,一个核心分子机制在形成隔离囊泡即自噬体中起着关键作用,自噬体是这一动态过程的标志性形态特征。其他成分使自噬能够适应细胞不断变化的需求。