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. 2018 Apr 25;10(4):747–763. doi: 10.18632/aging.101425

Figure 2.

Figure 2

Senescence was successfully induced in rat mesenchymal cell clone 2G11 cells. (A) Quantification of mRNA levels of senescence markers in 2G11 cells treated with H2O2. Data are expressed as means±SE (n=3); *P<0.05, ***P<0.001. (B) Quantification of mRNA levels of SASP markers in 2G11 cells treated with H2O2. IL-6: interleukin-6; TGFβ1: transforming growth factor β1; CCL2: C-C motif chemokine ligand 2. Data are expressed as means±SE (n=3); *P<0.05, ***P<0.001. (C) SA-βGal staining in 2G11 cells treated with or without H2O2. Arrowhead: SA-βGal+ cell. Scale bar: 50 μm. (D) Quantification of SA-βGal+ cells. Data are expressed as means±SE (n=3). (E) Immunocytochemical analysis of γH2AX in 2G11 cells treated with or without H2O2. Arrowhead: γH2AX+ cell. Scale bar: 50 μm. (F) Quantification of γH2AX+ cells. Data are expressed as means±SE (n=3); ***P<0.001.