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. 2017 Mar 30;8(3):e2710. doi: 10.1038/cddis.2017.135

Figure 5.

Figure 5

P65 inhibition by siRNA influences cell proliferation, apoptosis, and inflammation in vitro. (a) Fbs proliferation. (b) The apoptosis of Fbs by flow cytometry. The data are shown as the means±S.D. Statistical significance was calculated by one-way ANOVA for five independent samples. NS, no significance compared control group. *P<0.05 compared with NC group, #P<0.05 compared with NC+TGF-β1 group. (c) The RT-PCR analysis of the mRNA levels of p65, Col I, Col III, COX-2 and α-SMA expression in Fbs. The data are shown as the means±S.D. Statistical significance was calculated by one-way ANOVA for five independent samples. *P<0.05 compared with NC+TGF-β1 group. (d) Western blot analysis of the protein levels of p-p65, p65, Col I, Col III, COX-2 and α-SMA expression in Fbs. (e) Tcs cells (Tcs) proliferation. (f) The apoptosis of Fbs by flow cytometry. The data are shown as the means±S.D. Statistical significance was calculated using one-way ANOVA for five independent samples. $P<0.01 compared with NC group, &P<0.05 compared with NC+TGF-β1 group. (g) The RT-PCR analysis of the mRNA levels of p65, Col I, Col III, COX-2 and α-SMA expression in Tcs. The data are shown as the means±S.D. Statistical significance was calculated by one-way ANOVA for five independent samples. #P<0.05 compared with NC+TGF-β1 group. (h) Western blot analysis of the levels of p-p65, p65, Col I, Col III, COX-2 and α-SMA expression in Tcs