Department of Medical Genetics, Cambridge Institute for Medical Research, University of Cambridge, Addenbrookes Hospital, Hills Rd, Cambridge, UK.
Curr Opin Cell Biol. 2010 Apr;22(2):206-11. doi: 10.1016/j.ceb.2009.12.002. Epub 2010 Jan 4.
Macroautophagy (referred to as autophagy in this review) is a genetically regulated bulk degradation program conserved from yeast to humans, in which cytoplasmic substrates, such as damaged organelles and long-lived proteins, are delivered to lysosomes for degradation. In this review, we consider recent data that highlight possible mechanisms whereby autophagy mediates cytoprotective effects. These include the ability of autophagy to buffer against starvation, protect against apoptotic insults and clear mitochondria, aggregate-prone proteins and pathogens. These effects are pertinent to the roles of autophagy in normal human physiology, including the early neonatal period and ageing, as well as a variety of diseases, including cancer, neurodegenerative conditions and infectious diseases.
自噬(在本综述中称为自噬)是一种从酵母到人类中保守的遗传调控的细胞质大规模降解程序,在此过程中,细胞质底物,如受损的细胞器和长寿命蛋白,被递送至溶酶体进行降解。在本综述中,我们考虑了最近的数据,这些数据强调了自噬介导细胞保护作用的可能机制。这些机制包括自噬缓冲饥饿、抵抗凋亡损伤和清除线粒体、易于聚集的蛋白质和病原体的能力。这些效应与自噬在正常人体生理学中的作用有关,包括新生儿早期和衰老期,以及多种疾病,包括癌症、神经退行性疾病和传染病。