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Fig. 4. Effect of rMIS on cell viability and apoptotic activity in EGPF-YWK-II-overexpressing CHO cells. (A) Effect of rMIS and YWK-II proteins on cell viability. Cells transfected with EPGFP-YWK-II protein or EGFP and non-treated CHO cells were treated with different concentrations of rMIS for 3 days and assayed using the MTT method. The values obtained with the control untreated groups were set at 100% (*P<0.01). (B) Effect of rMIS on p53 levels in CHO cells. The established EGFP-YWK-II-overexpressing (YWK-II) and EGFP-transfected (EGFP) CHO cells and non-transfected CHO controls were cultured to confluence and incubated in serum-free medium for 24 hours prior to stimulation with 0.35 nM rMIS for 5 minutes. (C) Effect of rMIS on caspase-3 levels in YWK-II-overexpressing CHO cells. The cells were treated with 0.35 nM rMIS in the presence of YWK-II antibody (YWK-II Ab, 150 ng) or control IgG (150 ng) followed by western blot analysis of pro-caspase-3, with
-actin as the loading control.