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. 2011 Jan 5;6(1):e15808. doi: 10.1371/journal.pone.0015808

Figure 4. Effects of CMP1 deletion, CRZ1 deletion or expression of CaMCA1 on H2O2-induced apoptosis and caspase activity.

Figure 4

The wild-type (CAI4-EXP), cmp1Δ-EXP, crz1Δ-EXP, cmp1Δ-CMP1, crz1Δ-CRZ1 camca1Δ, CAI4-CaMCA1, cmp1Δ-CaMCA1 and crz1Δ-CaMCA1 cells were exposed to 2 mM H2O2 for 3 hours. In another experiment, the wild-type cells were exposed to 2 mM H2O2 for 3 hours in the presence of cyclosporin A (0.08 µM). (A) Percentage of cells that were classified as apoptotic by TUNEL assay was shown. (B) The caspase activity was determined by staining the cells with D2R. (C) Transcription level of CaMCA1 in response to 2 mM H2O2 for 3 hours was determined by real time RT-PCR. The mRNA levels were normalized on the basis of their ACT1 levels. Gene expression is indicated as the fold increase of the mutant and CaMCA1-introduced cells relative to that of the wild-type cells. The data are mean values ± S.D. from three independent experiments. * indicates P<0.01 compared with values of CAI4-EXP treated with H2O2 only. ** indicates P<0.01 compared with values of parental cells without CaMCA1.