Fig. 3.
Fig. 3. TPA and S-1P inhibit cyt c and Smac/DIABLO release, caspase-3 activation, and loss of viability in Jurkat cells induced by C6-ceramide. / (A) Cytosolic extracts from Jurkat cells treated for 5 hours with 25 μM C6-ceramide alone or after pretreatment with 50 nM TPA or 5 μM S-1P for 15 minutes were subjected to 15% SDS-PAGE and immunoblotted with anti-cyt c, anti-Smac/DIABLO, and anti-COX II, as described in Figure 1. (B) Proteins from duplicate extracts were analyzed by immunoblotting with anti–caspase-3 antibody. The mobilities of the 32-kd precursor (p32) and proteolytically processed forms (p20 and p17) are indicated. Similar results were obtained in 3 independent experiments. (C) Jurkat cells were treated for 5 hours, as described above. Loss of viability was assessed by the MTT assay. Samples were made in quadruplicate. Mean values with standard deviation are shown.

TPA and S-1P inhibit cyt c and Smac/DIABLO release, caspase-3 activation, and loss of viability in Jurkat cells induced by C6-ceramide.

(A) Cytosolic extracts from Jurkat cells treated for 5 hours with 25 μM C6-ceramide alone or after pretreatment with 50 nM TPA or 5 μM S-1P for 15 minutes were subjected to 15% SDS-PAGE and immunoblotted with anti-cyt c, anti-Smac/DIABLO, and anti-COX II, as described in Figure 1. (B) Proteins from duplicate extracts were analyzed by immunoblotting with anti–caspase-3 antibody. The mobilities of the 32-kd precursor (p32) and proteolytically processed forms (p20 and p17) are indicated. Similar results were obtained in 3 independent experiments. (C) Jurkat cells were treated for 5 hours, as described above. Loss of viability was assessed by the MTT assay. Samples were made in quadruplicate. Mean values with standard deviation are shown.

Close Modal

or Create an Account

Close Modal
Close Modal