Initiator cell death event induced by SARS-CoV-2 in the human airway epithelium.
Kaixin LiangKatherine C BarnettMartin HsuWei-Chun ChouSachendra S BaisKristina RiebeYuying XieTuong Thien NguyenThomas H OguinKevin M VannellaStephen M HewittDaniel S ChertowMaria BlasiGregory D SempowskiAmelia B KarlssonBeverly H KollerDeborah J LenschowScott H RandellJenny P Y TingPublished in: Science immunology (2024)
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.
Keyphrases
- sars cov
- cell death
- cell cycle arrest
- respiratory syndrome coronavirus
- angiotensin converting enzyme
- single cell
- endothelial cells
- angiotensin ii
- binding protein
- induced apoptosis
- pi k akt
- coronavirus disease
- nlrp inflammasome
- gene expression
- induced pluripotent stem cells
- rna seq
- oxidative stress
- endoplasmic reticulum stress
- hiv infected
- high throughput
- signaling pathway
- nucleic acid
- dendritic cells
- pluripotent stem cells
- bone marrow
- cell proliferation
- immune response
- circulating tumor cells