Fig. 1.
Fig. 1. Inhibition of neutrophil apoptosis by hypoxia. / Freshly isolated human peripheral blood neutrophils were incubated at 5 × 106 cells/mL in atmospheres containing 21% (open bars) or 3% oxygen (gray bars). At the time points indicated, cells were recovered and apoptosis was assessed (A) by morphologic examination of cytocentrifuge preparations, (B) by flow cytometry of annexin V binding, or (C) by flow cytometry following propidium iodide staining. Data in panel A represent the mean ± SEM of 3 separate experiments each performed in triplicate (*P < .05, compared with time-matched controls incubated in 21% oxygen). Data in panels B and C are representative flow-cytometry histograms; identical data were obtained in 4 additional independent experiments. (D) Classic neutrophil appearances following in vitro aging under normoxia and hypoxia are shown, and apoptotic cells are highlighted by arrowheads.

Inhibition of neutrophil apoptosis by hypoxia.

Freshly isolated human peripheral blood neutrophils were incubated at 5 × 106 cells/mL in atmospheres containing 21% (open bars) or 3% oxygen (gray bars). At the time points indicated, cells were recovered and apoptosis was assessed (A) by morphologic examination of cytocentrifuge preparations, (B) by flow cytometry of annexin V binding, or (C) by flow cytometry following propidium iodide staining. Data in panel A represent the mean ± SEM of 3 separate experiments each performed in triplicate (*P < .05, compared with time-matched controls incubated in 21% oxygen). Data in panels B and C are representative flow-cytometry histograms; identical data were obtained in 4 additional independent experiments. (D) Classic neutrophil appearances following in vitro aging under normoxia and hypoxia are shown, and apoptotic cells are highlighted by arrowheads.

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