坏死性下垂
上睑下垂
程序性细胞死亡
细胞凋亡
生物
呼吸上皮
病毒学
免疫学
冠状病毒
上皮
细胞生物学
疾病
医学
2019年冠状病毒病(COVID-19)
病理
传染病(医学专业)
遗传学
生物化学
作者
Kaixin Liang,Katherine C. Barnett,Martin Hsu,Wei-Chun Chou,Sachendra S. Bais,Kristina J. Riebe,Yuying Xie,Tuong T. Nguyen,Thomas H. Oguin,Kevin M. Vannella,Stephen M. Hewitt,Daniel S. Chertow,Maria Blasi,Gregory D. Sempowski,Amelia Karlsson,Beverly H. Koller,Deborah J. Lenschow,Scott H. Randell,Jenny P.‐Y. Ting
出处
期刊:Science immunology
[American Association for the Advancement of Science (AAAS)]
日期:2024-07-12
卷期号:9 (97)
被引量:2
标识
DOI:10.1126/sciimmunol.adn0178
摘要
Virus-induced cell death is a key contributor to COVID-19 pathology. Cell death induced by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is well studied in myeloid cells but less in its primary host cell type, angiotensin-converting enzyme 2 (ACE2)–expressing human airway epithelia (HAE). SARS-CoV-2 induces apoptosis, necroptosis, and pyroptosis in HAE organotypic cultures. Single-cell and limiting-dilution analysis revealed that necroptosis is the primary cell death event in infected cells, whereas uninfected bystanders undergo apoptosis, and pyroptosis occurs later during infection. Mechanistically, necroptosis is induced by viral Z-RNA binding to Z-DNA–binding protein 1 (ZBP1) in HAE and lung tissues from patients with COVID-19. The Delta (B.1.617.2) variant, which causes more severe disease than Omicron (B1.1.529) in humans, is associated with orders of magnitude–greater Z-RNA/ZBP1 interactions, necroptosis, and disease severity in animal models. Thus, Delta induces robust ZBP1-mediated necroptosis and more disease severity.
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