Fig. 6.
Fig. 6. Effect of Th1 cytokines on monocyte apoptosis induced by Fas crosslinking or by γ-irradiation. Monocytes (4 × 105 cells/mL) were cultured for 24 hours (in the absence of poly–L-lysine) either in the absence of any stimuli (medium), in the presence of an agonistic antibody to Fas (2 μg/mL), or after γ-irradiation (10 Gy). Addition of the Fas MoAb or γ-irradiation was performed either on monocytes incubated with medium alone (None) or on monocytes that had been preincubated for 1 hour with IL-12 (400 ng/mL) or with IFN-γ (100 IU/mL). Percentages of apoptotic cells were assessed by cytofluorimetry analysis using the nuclear dye acridine orange. These results are representative of three independent experiments, except for the effect of IFN-γ on Fas MoAb-induced apoptosis, which was found to vary (either enhancing or reducing apoptosis) in five different experiments (see Results and Discussion section).

Effect of Th1 cytokines on monocyte apoptosis induced by Fas crosslinking or by γ-irradiation. Monocytes (4 × 105 cells/mL) were cultured for 24 hours (in the absence of poly–L-lysine) either in the absence of any stimuli (medium), in the presence of an agonistic antibody to Fas (2 μg/mL), or after γ-irradiation (10 Gy). Addition of the Fas MoAb or γ-irradiation was performed either on monocytes incubated with medium alone (None) or on monocytes that had been preincubated for 1 hour with IL-12 (400 ng/mL) or with IFN-γ (100 IU/mL). Percentages of apoptotic cells were assessed by cytofluorimetry analysis using the nuclear dye acridine orange. These results are representative of three independent experiments, except for the effect of IFN-γ on Fas MoAb-induced apoptosis, which was found to vary (either enhancing or reducing apoptosis) in five different experiments (see Results and Discussion section).

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