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. 2022 Jan 25;12:1357. doi: 10.1038/s41598-022-04906-8

Figure 2.

Figure 2

Tmprss2 mRNA expression is upregulated in the lungs of ozone -exposed mice. FPKM values obtained from RNAseq data set obtained from airways (A), parenchyma (B), and alveolar macrophages (C) were used to quantify relative expression levels of Tmprss2 mRNA in air- versus ozone-exposed mice (n = 8). The data are expressed as mean (± SEM). Student’s t-Test; *P < 0.05, **P < 0.01, ****P < 0.0001. (D) RNAscope-based in situ hybridization for Tmprss2 transcripts (green dots representing punctate staining for Tmprss2 mRNA in airway epithelial cells (Top) and alveolar epithelial cells (bottom) in air- (left) and ozone-exposed (right) mice. All images were captured at the same magnification. FPKM values obtained from RNAseq data set obtained from airways (E), parenchyma (F), and alveolar macrophages (G) were used to quantify relative expression levels of Ace2 mRNA in air- versus ozone-exposed mice (n = 8). The data are expressed as means (± SEM). Student’s t-Test ** P < 0.01. (H) Duplex RNAscope-based in situ hybridization for Tmprss2 (green puncta, green arrow) and Ace2 (red puncta, red arrow) in the airways of air- (left) and ozone-exposed (right) mice. All images were captured at the same magnification.