Experimental Model of Pulmonary Inflammation Induced by SARS-CoV-2 Spike Protein and Endotoxin.

Puthia M, Tanner L, Petruk G, Schmidtchen A

ACS Pharmacol. Transl. Sci. 5 (3) 141-148 [2022-03-11; online 2022-01-25]

COVID-19 is characterized by a dysregulated and excessive inflammatory response and, in severe cases, acute respiratory distress syndrome. We have recently demonstrated a previously unknown high-affinity interaction between the SARS-CoV-2 spike (S) protein and bacterial lipopolysaccharide (LPS), leading to the boosting of inflammation. Here we present a mouse inflammation model employing the coadministration of aerosolized S protein together with LPS to the lungs. Using NF-κB-RE-Luc reporter and C57BL/6 mice followed by combinations of bioimaging, cytokine, chemokine, fluorescence-activated cell sorting, and histochemistry analyses, we show that the model yields severe pulmonary inflammation and a cytokine profile similar to that observed in COVID-19. Therefore, the model offers utility for analyses of the pathophysiological features of COVID-19 and the development of new treatments.

Category: Biochemistry

Category: Health

Funder: VR

Type: Journal article

PubMed 35774232

DOI 10.1021/acsptsci.1c00219

Crossref 10.1021/acsptsci.1c00219

pmc: PMC9239546


Publications 8.1.0