Skip to main content
. 2022 Dec 23;13:7907. doi: 10.1038/s41467-022-35590-x

Fig. 4. MT1-MMP-mediated ACE2 shedding mediates the SARS-CoV-2 cell entry in vitro and in vivo.

Fig. 4

a–c The A549 and HEK293T cells were inoculated with rACE21-706, followed by SARS-CoV-2 infection. Vehicle-treated cells served as a control. The viral antigens of these cells were detected by immunostaining of Nucleocapsid Protein (NP) (green) as shown in a. (One representative data was shown from three independently repeated experiments) (Scale bar: 20 μm) The viral gene copies of these cells were measured by qPCR analyses of the SARS-CoV-2 genes as shown in b and c. (n = 3 biologically independent experiments) d Experimental strategy to study the role of human solACE in mediating SARS-CoV-2 infection in mice. e Immunostaining of human ACE2 (red) and SARS-CoV-2 (green) Nucleocapsid Protein (NP) in lung sections of mice expressing solACE21-706/ solACE21-740/ACE2full length (FL) (n = 8 for AAV-control; n = 8 for AAV-hACE2(1-706); n = 8 for AAV-hACE2 (1-740); n = 8 for AAV-hACE2(full length)). (Scale bar: 20 μm) f The viral loads in the lungs of mice expressing solACE21-706/ solACE21-740/ ACE2full length (FL) were measured by qPCR analyses of the SARS-CoV-2 genes (n = 8 for AAV-control; n = 8 for AAV-hACE2(1-706); n = 8 for AAV-hACE2 (1-740); n = 8 for AAV-hACE2(full length)). g Summary histology scores determined in the lung tissues of mice expressing solACE21-706/ solACE21-740/ACE2full length (FL) (n = 8 for AAV-control; n = 8 for AAV-hACE2(1-706); n = 8 for AAV-hACE2 (1-740); n = 8 for AAV-hACE2(full length)) h Representative Hematoxylin-eosin (HE) staining of lungs of mice expressing solACE21-706/ solACE21-740/ACE2full length (FL) (n = 8 for AAV-control; n = 8 for AAV-hACE2(1-706); n = 8 for AAV-hACE2 (1-740); n = 8 for AAV-hACE2(full length)). (Scale bar: 50 μm) Data are means ± S.E.M. of three independent repeats. Statistical analyses were performed by one way ANOVA for (b, c; f, g) Source data are provided as a Source Data file.