Table 1.

Cell-labeling results indicating facilitation by bisindolylmaleimide (Bis) of CD95-mediated apoptosis in human dendritic cells (DC)

Treatment of DC Cell-labeling results (% DC)*PI+Hypodiploid nuclei (%)
Annexin V PIAnnexin V+ PIAnnexin V+ PI+
Medium  87.2 ± 2.5 3.3 ± 0.7  7.8 ± 1.6  1.6 ± 0.2  3.8 ± 0.8 
Anti-CD95  85.8 ± 2.8  3.7 ± 0.8  8.6 ± 1.8 1.9 ± 0.4  8.8 ± 2.4  
Bis  84.7 ± 4.3 6.3 ± 1.3  7.4 ± 2.6  1.6 ± 0.5  9.6 ± 1.9 
Bis + Anti-CD95  52.6 ± 1.4  12.4 ± 2.6 22.4 ± 1.3 12.4 ± 3.0 46.1 ± 6.71-153 
Treatment of DC Cell-labeling results (% DC)*PI+Hypodiploid nuclei (%)
Annexin V PIAnnexin V+ PIAnnexin V+ PI+
Medium  87.2 ± 2.5 3.3 ± 0.7  7.8 ± 1.6  1.6 ± 0.2  3.8 ± 0.8 
Anti-CD95  85.8 ± 2.8  3.7 ± 0.8  8.6 ± 1.8 1.9 ± 0.4  8.8 ± 2.4  
Bis  84.7 ± 4.3 6.3 ± 1.3  7.4 ± 2.6  1.6 ± 0.5  9.6 ± 1.9 
Bis + Anti-CD95  52.6 ± 1.4  12.4 ± 2.6 22.4 ± 1.3 12.4 ± 3.0 46.1 ± 6.71-153 

DC were incubated for 18 hours in medium alone or in the presence of either CH-11 anti-CD95 monoclonal antibody (1 μg/mL) or Bis III (20 μmol/L).

*

DC were stained with fluorescein isothiocyanate-conjugated (FITC) annexin V followed by propidium iodide (PI) and analyzed with use of flow cytometry. Data represent mean (±SEM) percentage of cells in each quadrant of dot-plot analysis from 6 independent experiments on samples from 6 different donors.

P < .05 compared with DC incubated in medium alone (Wilcoxon two-tailed test).

DC were fixed before incubation with PI and RNase. Data represent mean (±SEM) percentage of hypodiploid nuclei measured by flow cytometry in 9 independent experiments on samples from 9 different donors.

F1-153

P < .005 compared with DC incubated in medium alone (Wilcoxon two-tailed test).

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