Figure 6.
Figure 6. Peroxide accumulation and effects of hydrogen peroxide. (A) Intracellular peroxide accumulation in untreated U-937 cells (Cont), in cells treated for 14 hours with LY294002 alone, and in cells treated for 14 hours with 4 μMAs2O3, alone or in combination with LY294002, as determined by flow cytometry after cell loading with H2DCFDA. The vertical, dotted lines represent the mean fluorescence value in the control, to better discern the displacement caused by the treatments. (B) Frequency of apoptotic cells (mean ± standard deviation of at least 4 determinations) in U-937 cell cultures treated for 24 hours with 20 and 40 μM H2O2 alone, and with 1 to 4 μ As2O3, camptothecin, and cisplatin, either alone (-) or in combination with H2O2. All other conditions were as in Figure 1.

Peroxide accumulation and effects of hydrogen peroxide. (A) Intracellular peroxide accumulation in untreated U-937 cells (Cont), in cells treated for 14 hours with LY294002 alone, and in cells treated for 14 hours with 4 μMAs2O3, alone or in combination with LY294002, as determined by flow cytometry after cell loading with H2DCFDA. The vertical, dotted lines represent the mean fluorescence value in the control, to better discern the displacement caused by the treatments. (B) Frequency of apoptotic cells (mean ± standard deviation of at least 4 determinations) in U-937 cell cultures treated for 24 hours with 20 and 40 μM H2O2 alone, and with 1 to 4 μ As2O3, camptothecin, and cisplatin, either alone (-) or in combination with H2O2. All other conditions were as in Figure 1.

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