Department of Biochemistry and Cell Biology, National Institute of Infectious Diseases, Toyama, Shinjyuku, Tokyo, Japan.
Microbiol Immunol. 2011 Jan;55(1):1-11. doi: 10.1111/j.1348-0421.2010.00271.x.
Autophagy (macroautophagy) is a dynamic process for degradation of cytosolic components. Autophagy has intracellular anti-viral and anti-bacterial functions, and plays a role in the initiation of innate and adaptive immune system responses to viral and bacterial infections. Some viruses encode virulence factors for blocking autophagy, whereas others utilize some autophagy components for their intracellular growth or cellular budding. The "core" autophagy-related (Atg) complexes in mammals are ULK1 protein kinase, Atg9-WIPI-1 and Vps34-beclin1 class III PI3-kinase complexes, and the Atg12 and LC3 conjugation systems. In addition, PI(3)-binding proteins, PI3-phosphatases, and Rab proteins contribute to autophagy. The autophagy process consists of continuous dynamic membrane formation and fusion. In this review, the relationships between these Atg complexes and each process are described. Finally, the critical points for monitoring autophagy, including the use of GFP-LC3 and GFP-Atg5, are discussed.
自噬(巨自噬)是一种降解胞质成分的动态过程。自噬具有细胞内抗病毒和抗细菌功能,并在启动对病毒和细菌感染的先天和适应性免疫系统反应中发挥作用。一些病毒编码了用于阻断自噬的毒力因子,而另一些病毒则利用一些自噬成分进行其细胞内生长或细胞出芽。哺乳动物中的“核心”自噬相关(Atg)复合物是 ULK1 蛋白激酶、Atg9-WIPI-1 和 Vps34-beclin1 类 III PI3-激酶复合物,以及 Atg12 和 LC3 连接系统。此外,PI(3)结合蛋白、PI3-磷酸酶和 Rab 蛋白有助于自噬。自噬过程包括连续的动态膜形成和融合。在这篇综述中,描述了这些 Atg 复合物与各个过程之间的关系。最后,讨论了监测自噬的关键点,包括使用 GFP-LC3 和 GFP-Atg5。