Fig. 4.
Fig. 4. Inhibition of apoptosis, PS externalization, and CPP32 processing by inhibitors of ICE family proteases. U937 cells were treated with 10 μg/mL etoposide in the presence of indicated concentrations of Z-Asp (circles) and Z-VAD (squares) for 4 hours. The development of apoptosis (open symbols) and PS externalization (solid symbols) were analyzed using a flow cytometer (A), and CPP32 processing was examined by Western blot analysis (B). CPP32 processing to the p20 and p17 fragments is presented. Lane 1, no inhibitor; lanes 2 through 4, Z-Asp at 10, 30, and 100 μg/mL, respectively; lanes 5 through 7, Z-VAD at 10, 30, and 100 μg/mL, respectively. The experiments were repeated three times and similar results were obtained.

Inhibition of apoptosis, PS externalization, and CPP32 processing by inhibitors of ICE family proteases. U937 cells were treated with 10 μg/mL etoposide in the presence of indicated concentrations of Z-Asp (circles) and Z-VAD (squares) for 4 hours. The development of apoptosis (open symbols) and PS externalization (solid symbols) were analyzed using a flow cytometer (A), and CPP32 processing was examined by Western blot analysis (B). CPP32 processing to the p20 and p17 fragments is presented. Lane 1, no inhibitor; lanes 2 through 4, Z-Asp at 10, 30, and 100 μg/mL, respectively; lanes 5 through 7, Z-VAD at 10, 30, and 100 μg/mL, respectively. The experiments were repeated three times and similar results were obtained.

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