自噬
生物
病毒病机
冠状病毒
病毒复制
病毒
病毒学
病毒生命周期
细胞生物学
机制(生物学)
发病机制
2019年冠状病毒病(COVID-19)
疾病
免疫学
遗传学
传染病(医学专业)
医学
细胞凋亡
病理
哲学
认识论
作者
Katelyn Miller,Marisa E. McGrath,Zhiqiang Hu,Sohha Ariannejad,Stuart Weston,Matthew B. Frieman,William T. Jackson
出处
期刊:Autophagy
[Taylor & Francis]
日期:2020-09-23
卷期号:16 (12): 2131-2139
被引量:139
标识
DOI:10.1080/15548627.2020.1817280
摘要
The COVID-19 pandemic, caused by the SARS-CoV-2 virus, is the most recent example of an emergent coronavirus that poses a significant threat to human health. Virus-host interactions play a major role in the viral life cycle and disease pathogenesis, and cellular pathways such as macroautophagy/autophagy prove to be either detrimental or beneficial to viral replication and maturation. Here, we describe the literature over the past twenty years describing autophagy-coronavirus interactions. There is evidence that many coronaviruses induce autophagy, although some of these viruses halt the progression of the pathway prior to autophagic degradation. In contrast, other coronaviruses usurp components of the autophagy pathway in a non-canonical fashion. Cataloging these virus-host interactions is crucial for understanding disease pathogenesis, especially with the global challenge of SARS-CoV-2 and COVID-19. With the recognition of autophagy inhibitors, including the controversial drug chloroquine, as possible treatments for COVID-19, understanding how autophagy affects the virus will be critical going forward.
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