病毒感染期间的自噬作用——一把双刃剑。
Autophagy during viral infection - a double-edged sword.
机构信息
Department of Molecular Microbiology and Immunology, Keck School of Medicine, University of Southern California, Zilkha Neurogenetic Institute, Los Angeles, CA, USA.
出版信息
Nat Rev Microbiol. 2018 Jun;16(6):341-354. doi: 10.1038/s41579-018-0003-6.
Autophagy is a powerful tool that host cells use to defend against viral infection. Double-membrane vesicles, termed autophagosomes, deliver trapped viral cargo to the lysosome for degradation. Specifically, autophagy initiates an innate immune response by cooperating with pattern recognition receptor signalling to induce interferon production. It also selectively degrades immune components associated with viral particles. Following degradation, autophagy coordinates adaptive immunity by delivering virus-derived antigens for presentation to T lymphocytes. However, in an ongoing evolutionary arms race, viruses have acquired the potent ability to hijack and subvert autophagy for their benefit. In this Review, we focus on the key regulatory steps during viral infection in which autophagy is involved and discuss the specific molecular mechanisms that diverse viruses use to repurpose autophagy for their life cycle and pathogenesis.
自噬是宿主细胞用来防御病毒感染的一种强大工具。双层膜囊泡,称为自噬体,将捕获的病毒货物递送至溶酶体进行降解。具体来说,自噬通过与模式识别受体信号合作来诱导干扰素产生,从而引发先天免疫反应。它还选择性地降解与病毒颗粒相关的免疫成分。降解后,自噬通过递呈病毒衍生的抗原来协调适应性免疫,以供 T 淋巴细胞呈递。然而,在持续的进化军备竞赛中,病毒已经获得了劫持和颠覆自噬以谋取自身利益的强大能力。在这篇综述中,我们重点关注病毒感染过程中涉及自噬的关键调节步骤,并讨论各种病毒利用自噬来实现其生命周期和发病机制的特定分子机制。