Effect of SARS-CoV-2 S protein on the proteolytic cleavage of the epithelial Na+ channel ENaC

PLoS One. 2024 Apr 25;19(4):e0302436. doi: 10.1371/journal.pone.0302436. eCollection 2024.

Abstract

Severe cases of COVID-19 are characterized by development of acute respiratory distress syndrome (ARDS). Water accumulation in the lungs is thought to occur as consequence of an exaggerated inflammatory response. A possible mechanism could involve decreased activity of the epithelial Na+ channel, ENaC, expressed in type II pneumocytes. Reduced transepithelial Na+ reabsorption could contribute to lung edema due to reduced alveolar fluid clearance. This hypothesis is based on the observation of the presence of a novel furin cleavage site in the S protein of SARS-CoV-2 that is identical to the furin cleavage site present in the alpha subunit of ENaC. Proteolytic processing of αENaC by furin-like proteases is essential for channel activity. Thus, competition between S protein and αENaC for furin-mediated cleavage in SARS-CoV-2-infected cells may negatively affect channel activity. Here we present experimental evidence showing that coexpression of the S protein with ENaC in a cellular model reduces channel activity. In addition, we show that bidirectional competition for cleavage by furin-like proteases occurs between 〈ENaC and S protein. In transgenic mice sensitive to lethal SARS-CoV-2, however, a significant decrease in gamma ENaC expression was not observed by immunostaining of lungs infected as shown by SARS-CoV2 nucleoprotein staining.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alveolar Epithelial Cells / metabolism
  • Alveolar Epithelial Cells / virology
  • Animals
  • COVID-19* / metabolism
  • COVID-19* / virology
  • Epithelial Sodium Channels* / metabolism
  • Furin* / metabolism
  • HEK293 Cells
  • Humans
  • Lung / metabolism
  • Lung / pathology
  • Lung / virology
  • Mice
  • Mice, Transgenic*
  • Proteolysis*
  • SARS-CoV-2* / metabolism
  • SARS-CoV-2* / pathogenicity
  • Spike Glycoprotein, Coronavirus* / metabolism

Substances

  • Epithelial Sodium Channels
  • Furin
  • Spike Glycoprotein, Coronavirus
  • spike protein, SARS-CoV-2