Fig. 8.
Fig. 8. Time course of lymphoma cell permeabilization and phagocytosis following H2O2 treatment. / JLP 119 cells (A) or BL-41 cells (B) were treated with 75 or 250 μmol/L H2O2, respectively, and allowed to incubate for the times indicated in the figure. Cells were then harvested and incubated with monocyte-derived macrophages for 1 hour. Percent phagocytosis (open circles) was analyzed as described in “Materials and methods.” Cell death was quantified by Hoechst/PI staining. The total percentage of cells that had become permeable to PI is shown (closed circles). Under these conditions, at least 82% of the PI-permeable cells at each time point were pyknotic/necrotic. The results for JLP 119 are averaged from 2 separate experiments, and those for BL-41 are from a single experiment.

Time course of lymphoma cell permeabilization and phagocytosis following H2O2 treatment.

JLP 119 cells (A) or BL-41 cells (B) were treated with 75 or 250 μmol/L H2O2, respectively, and allowed to incubate for the times indicated in the figure. Cells were then harvested and incubated with monocyte-derived macrophages for 1 hour. Percent phagocytosis (open circles) was analyzed as described in “Materials and methods.” Cell death was quantified by Hoechst/PI staining. The total percentage of cells that had become permeable to PI is shown (closed circles). Under these conditions, at least 82% of the PI-permeable cells at each time point were pyknotic/necrotic. The results for JLP 119 are averaged from 2 separate experiments, and those for BL-41 are from a single experiment.

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