Eskelinen Eeva-Liisa, Saftig Paul
Department of Biological and Environmental Sciences, Division of Biochemistry, University of Helsinki, PO Box 56, FIN-00014 Helsinki, Finland.
Biochim Biophys Acta. 2009 Apr;1793(4):664-73. doi: 10.1016/j.bbamcr.2008.07.014. Epub 2008 Jul 28.
Autophagy delivers cytoplasmic material and organelles to lysosomes for degradation. The formation of autophagosomes is controlled by a specific set of autophagy genes called atg genes. The magnitude of autophagosome formation is tightly regulated by intracellular and extracellular amino acid concentrations and ATP levels via signaling pathways that include the nutrient sensing kinase TOR. Autophagy functions as a stress response that is upregulated by starvation, oxidative stress, or other harmful conditions. Remarkably, autophagy has been shown to possess important housekeeping and quality control functions that contribute to health and longevity. Autophagy plays a role in innate and adaptive immunity, programmed cell death, as well as prevention of cancer, neurodegeneration and aging. In addition, impaired autophagic degradation contributes to the pathogenesis of several human diseases including lysosomal storage disorders and muscle diseases.
自噬将细胞质物质和细胞器输送到溶酶体进行降解。自噬体的形成由一组特定的自噬基因(称为atg基因)控制。自噬体形成的程度通过包括营养感应激酶TOR在内的信号通路,受到细胞内和细胞外氨基酸浓度以及ATP水平的严格调控。自噬作为一种应激反应,在饥饿、氧化应激或其他有害条件下会上调。值得注意的是,自噬已被证明具有重要的看家及质量控制功能,对健康和长寿有益。自噬在固有免疫和适应性免疫、程序性细胞死亡以及预防癌症、神经退行性变和衰老中发挥作用。此外,自噬性降解受损会导致包括溶酶体贮积症和肌肉疾病在内的几种人类疾病的发病机制。