Figure 6
(A) Representative images of Western blot analysis on Calu-3 sublines treated with 100 ng/ml IFNγ for 30 min. Calu-3P cells without the treatment (0 h) and with the treatment for 48 h were used for monitoring protein phosphorylation as indicated. Both pStat1Tyr701 and pStat1Ser727 were increased upon IFNγ treatment, while phosphorylation of Stat1Ser727 sustained for at least 48 h. (B–D) Bar graphs of phosphorylated proteins in (A), * denotes P<0.05, as compared with the vector control (V).
Prostasin activation of MAPK pathway manifested by ERK1/2 phosphorylation

(A) Representative images of Western blot analysis on Calu-3 sublines treated with 100 ng/ml IFNγ for 30 min. Calu-3P cells without the treatment (0 h) and with the treatment for 48 h were used for monitoring protein phosphorylation as indicated. Both pStat1Tyr701 and pStat1Ser727 were increased upon IFNγ treatment, while phosphorylation of Stat1Ser727 sustained for at least 48 h. (B–D) Bar graphs of phosphorylated proteins in (A), * denotes P<0.05, as compared with the vector control (V).

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