Skip to main content
. 2024 Jul 23;14:16895. doi: 10.1038/s41598-024-66473-4

Figure 3.

Figure 3

Wuhan-Hu-1 [S1S2] spike and β-1.351 [S1S2] spike proteins suppress CFTR protein expression in differentiated BCi.NS1.1 (d-BCi) epithelia. (a) ALI differentiated dBCi cells were incubated apically with different concentrations of Wuhan-Hu-1 [S1S2] spike protein for 4 h, washed and then incubated for additional 20 h under ALI conditions. Representative Western blot images (left panel) and densitometric analysis of the expression levels of CFTR (right panel) in treated dBCi cells after Ussing chamber analyses are shown. β-actin was used for equal loading of protein. (b) dBCi cells were incubated with different concentrations of β-1.351 [S1S2] spike protein and analyzed as in part (a). The data are expressed as means ± SD (N = 4). Statistical p values were determined with a one-way ANOVA, followed by both Holm’s and Dunnett’s post-hoc tests comparing each mean to the medium control. For the Holm test, *, p < 0.05; and ¥, p < 0.01. Dunnett’s tests were consistently significant (p < 0.05), except as noted (•).