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. 2013 Jan 31;1(1):8–16. doi: 10.1016/j.redox.2012.11.004

Fig. 2.

Fig. 2

Differential responses of LPDL (non-senescent) and HPDL (senescent) HDFs to H2O2 induced apoptosis.

A, H2O2 at 100 μM or 200 μM was used to induce apoptosis in LPDL or HPDL. LPDL and HPDL fibroblasts were subjected to Annexin-V FITC assay 24 h after 2 h treatment of H2O2. Percentage (mean±SD) of fibroblasts apoptosis are measured by flow cytometry, results are average of at least three independent experiments. B, Caspase-3 activity assay. LPDL and HPDL HDFs were subjected to caspsae-3 activity assay 24 h after induced apoptosis with or without H2O2 at 100 μM for 2 h. Results are average± SD of caspse-3 activity of at least three independent experiments. p<0.05: 24 h after 2 h treatment of 100 μm or 200 μM H2O2vs. its own group untreated control.