Fig. 3.
Fig. 3. Ability of prolonged hypoxic exposure to impair the subsequent rate of neutrophil apoptosis following reoxygenation. / Neutrophils were incubated for 20 to 30 hours in 21% (▪) or 3% (●) oxygen, and apoptosis was assessed morphologically on cytocentrifuge preparations. In addition, the extent of apoptosis was assessed in cells initially incubated in 3% oxygen for 20 hours before transfer to 21% oxygen (▵). Data are expressed as mean ± SEM of 5 separate experiments, each performed in triplicate.

Ability of prolonged hypoxic exposure to impair the subsequent rate of neutrophil apoptosis following reoxygenation.

Neutrophils were incubated for 20 to 30 hours in 21% (▪) or 3% (●) oxygen, and apoptosis was assessed morphologically on cytocentrifuge preparations. In addition, the extent of apoptosis was assessed in cells initially incubated in 3% oxygen for 20 hours before transfer to 21% oxygen (▵). Data are expressed as mean ± SEM of 5 separate experiments, each performed in triplicate.

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