SARS-CoV-2 Spike Protein Induces Oxidative Stress and Senescence in Mouse and Human Lung

In Vivo. 2024 Jul-Aug;38(4):1546-1556. doi: 10.21873/invivo.13605.

Abstract

Background/aim: There is concern that people who had COVID-19 will develop pulmonary fibrosis. Using mouse models, we compared pulmonary inflammation following injection of the spike protein of SARS-CoV-2 (COVID-19) to radiation-induced inflammation to demonstrate similarities between the two models. SARS-CoV-2 (COVID-19) induces inflammatory cytokines and stress responses, which are also common to ionizing irradiation-induced acute pulmonary damage. Cellular senescence, which is a late effect following exposure to SARS-CoV-2 as well as radiation, was investigated.

Materials and methods: We evaluated the effect of SARS-CoV-2 spike protein compared to ionizing irradiation in K18-hACE2 mouse lung, human lung cell lines, and in freshly explanted human lung. We measured reactive oxygen species, DNA double-strand breaks, stimulation of transforming growth factor-beta pathways, and cellular senescence following exposure to SARS-CoV-2 spike protein, irradiation or SARS-COV-2 and irradiation. We also measured the effects of the antioxidant radiation mitigator MMS350 following irradiation or exposure to SARS-CoV-2.

Results: SARS-CoV-2 spike protein induced reactive oxygen species, DNA double-strand breaks, transforming growth factor-β signaling pathways, and senescence, which were exacerbated by prior or subsequent ionizing irradiation. The water-soluble radiation countermeasure, MMS350, reduced spike protein-induced changes.

Conclusion: In both the SARS-Co-2 and the irradiation mouse models, similar responses were seen indicating that irradiation or exposure to SARS-CoV-2 virus may lead to similar lung diseases such as pulmonary fibrosis. Combination of irradiation and SARS-CoV-2 may result in a more severe case of pulmonary fibrosis. Cellular senescence may explain some of the late effects of exposure to SARS-CoV-2 spike protein and to ionizing irradiation.

Keywords: COVID-19; Reactive oxygen species; oxidative stress; spike protein.

MeSH terms

  • Animals
  • COVID-19* / virology
  • Cell Line
  • Cellular Senescence* / radiation effects
  • DNA Breaks, Double-Stranded / radiation effects
  • Disease Models, Animal
  • Humans
  • Lung* / metabolism
  • Lung* / pathology
  • Lung* / radiation effects
  • Lung* / virology
  • Mice
  • Oxidative Stress* / radiation effects
  • Reactive Oxygen Species* / metabolism
  • SARS-CoV-2*
  • Spike Glycoprotein, Coronavirus* / metabolism
  • Transforming Growth Factor beta / metabolism

Substances

  • Spike Glycoprotein, Coronavirus
  • spike protein, SARS-CoV-2
  • Reactive Oxygen Species
  • Transforming Growth Factor beta