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. 2018 May 21;26(3):394–403. doi: 10.1177/1933719118776790

Figure 5.

Figure 5.

The increased cell senescence, p38 mitogen-activated protein kinase (MAPK) phosphorylation, and downregulated sirtuin 3 (SIRT3) expression induced by hydrogen peroxide (H2O2) were enhanced in PGRMC1 knockdown chorion cells. A, Senescence cell histochemical staining of chorion cells treated with 0 and 300 μM H2O2 for 24 hours in scrambled small-interfering RNA (siRNA)-transfected chorion cells (CsiRNA) and in PGRMC1 knockdown cells (PsiRNA). SA-β-Gal-positive chorion cells are blue in representative images. B, The proportion of SA-β-Gal-positive chorion cells is summarized in a bar graph. C, Representative Western blot image to demonstrate the p38 MAPK phosphorylation under 300 μM H2O2 treatment at 30 minutes in CsiRNA and PsiRNA groups. Densitometry analysis was summarized in a bar graph (N = 8). D, Representative Western blot image to demonstrate SIRT3 protein expression in CsiRNA and PsiRNA groups and densitometry analysis was summarized in a bar graph (N = 10). MAPK indicates mitogen-activated protein kinases; H2O2, hydrogen peroxide; PGRMC1, progesterone receptor membrane component 1; siRNA, small-interfering RNA; SIRT3, sirtuin 3.