Viral Immunobiology, Institute of Experimental Immunology, University of Zürich, Winterthurerstrasse 190, CH-8057 Zürich, Switzerland.
Viruses. 2011 Jul;3(7):1166-78. doi: 10.3390/v3071166. Epub 2011 Jul 12.
Macroautophagy is a catabolic pathway in eukaryotic cells that has recently been shown to facilitate pathogen detection, pathogen restriction and pathogen-derived antigen presentation to CD4(+) T cells. Due to these protective functions during immune responses, several pathogens, including RNA and DNA viruses, have developed strategies to inhibit autophagosome generation or maturation. Interestingly, most of the respective viral proteins exert these functions via binding to Beclin-1, an essential macroautophagy protein that constitutes part of the phosphatidylinositol-3 kinase complexes that mark membranes for autophagosome generation and facilitate autophagosome fusion with lyososomes. The viruses that inhibit macroautophagy by this pathway include herpesviruses, HIV and influenza A virus. Inhibition either before or after autophagosome formation seems to benefit their viral replication by different mechanisms, which are discussed here.
自噬是真核细胞中的一种分解代谢途径,最近的研究表明,它有助于病原体的检测、限制和向 CD4(+)T 细胞呈递病原体衍生的抗原。由于在免疫反应中具有这些保护功能,几种病原体,包括 RNA 和 DNA 病毒,已经开发出抑制自噬体生成或成熟的策略。有趣的是,大多数相应的病毒蛋白通过与 Beclin-1 结合来发挥这些功能,Beclin-1 是一种必需的自噬蛋白,它构成了参与标记自噬体生成的膜的磷脂酰肌醇-3 激酶复合物的一部分,并促进自噬体与溶酶体融合。通过这种途径抑制自噬的病毒包括疱疹病毒、HIV 和甲型流感病毒。自噬体形成前后的抑制似乎通过不同的机制有利于它们的病毒复制,这在本文中进行了讨论。