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10.3390/cells11081347

http://scihub22266oqcxt.onion/10.3390/cells11081347
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35456026!9028056!35456026
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suck abstract from ncbi

pmid35456026      Cells 2022 ; 11 (8): ?
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  • CFTR Modulation Reduces SARS-CoV-2 Infection in Human Bronchial Epithelial Cells #MMPMID35456026
  • Lotti V; Merigo F; Lagni A; Di Clemente A; Ligozzi M; Bernardi P; Rossini G; Concia E; Plebani R; Romano M; Sbarbati A; Sorio C; Gibellini D
  • Cells 2022[Apr]; 11 (8): ? PMID35456026show ga
  • People with cystic fibrosis should be considered at increased risk of developing severe symptoms of COVID-19. Strikingly, a broad array of evidence shows reduced spread of SARS-CoV-2 in these subjects, suggesting a potential role for CFTR in the regulation of SARS-CoV-2 infection/replication. Here, we analyzed SARS-CoV-2 replication in wild-type and CFTR-modified human bronchial epithelial cell lines and primary cells to investigate SARS-CoV-2 infection in people with cystic fibrosis. Both immortalized and primary human bronchial epithelial cells expressing wt or F508del-CFTR along with CRISPR/Cas9 CFTR-ablated clones were infected with SARS-CoV-2 and samples were harvested before and from 24 to 72 h post-infection. CFTR function was also inhibited in wt-CFTR cells with the CFTR-specific inhibitor IOWH-032 and partially restored in F508del-CFTR cells with a combination of CFTR modulators (VX-661+VX-445). Viral load was evaluated by real-time RT-PCR in both supernatant and cell extracts, and ACE-2 expression was analyzed by both western blotting and flow cytometry. SARS-CoV-2 replication was reduced in CFTR-modified bronchial cells compared with wild-type cell lines. No major difference in ACE-2 expression was detected before infection between wild-type and CFTR-modified cells, while a higher expression in wild-type compared to CFTR-modified cells was detectable at 72 h post-infection. Furthermore, inhibition of CFTR channel function elicited significant inhibition of viral replication in cells with wt-CFTR, and correction of CFTR function in F508del-CFTR cells increased the release of SARS-CoV-2 viral particles. Our study provides evidence that CFTR expression/function is involved in the regulation of SARS-CoV-2 replication, thus providing novel insights into the role of CFTR in SARS-CoV-2 infection and the development of therapeutic strategies for COVID-19.
  • |*COVID-19[MESH]
  • |*Cystic Fibrosis Transmembrane Conductance Regulator/genetics/metabolism[MESH]
  • |*Cystic Fibrosis/metabolism[MESH]
  • |Epithelial Cells/metabolism[MESH]
  • |Humans[MESH]


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