Department of Medical Genetics, Cambridge Institute for Medical Research, University of Cambridge, Wellcome Trust/MRC Building, Cambridge Biomedical Campus, Cambridge CB2 0XY, United Kingdom; email:
Annu Rev Biochem. 2016 Jun 2;85:685-713. doi: 10.1146/annurev-biochem-060815-014556. Epub 2016 Feb 8.
Autophagy is a conserved intracellular pathway that delivers cytoplasmic contents to lysosomes for degradation via double-membrane autophagosomes. Autophagy substrates include organelles such as mitochondria, aggregate-prone proteins that cause neurodegeneration and various pathogens. Thus, this pathway appears to be relevant to the pathogenesis of diverse diseases, and its modulation may have therapeutic value. Here, we focus on the cell and molecular biology of mammalian autophagy and review the key proteins that regulate the process by discussing their roles and how these may be modulated by posttranslational modifications. We consider the membrane-trafficking events that impact autophagy and the questions relating to the sources of autophagosome membrane(s). Finally, we discuss data from structural studies and some of the insights these have provided.
自噬是一种保守的细胞内途径,通过双层自噬体将细胞质内容物递送至溶酶体进行降解。自噬底物包括线粒体等细胞器、易聚集导致神经退行性变的蛋白质和各种病原体。因此,该途径似乎与多种疾病的发病机制有关,其调节可能具有治疗价值。在这里,我们专注于哺乳动物自噬的细胞和分子生物学,通过讨论其作用以及这些作用如何通过翻译后修饰来调节,来回顾调节该过程的关键蛋白。我们考虑影响自噬的膜转运事件以及与自噬体膜来源相关的问题。最后,我们讨论结构研究的数据以及这些研究提供的一些见解。