Figure 5From: Regulation of apoptosis and priming of neutrophil oxidative burst by diisopropyl fluorophosphateEffect of DFP on PMN oxidative burst activity and hydrogen peroxide production. Human neutrophils were incubated alone (Control), with LPS (1 μg/mL) or with DFP (2.5 mM) for 2 hours. Cells were then incubated with 1 μM of DHR followed by incubation with 10-7 M fMLP. Cells were analyzed by flow cytometry to detect the conversion of DHR 123 to rhodamine 123. A. Mean fluorescence values are shown for a minimum of 10 000 cells for each condition and are representative of 9 separate experiments. B. Oxidative burst activity of neutrophils treated with or without LPS or DFP (2.5 mM). Data represent mean ± SD of 9 separate experiments. *P < 0.002. C. Neutrophils were incubated alone (control), with LPS (1 μg/mL) or with DFP (2.5 mM) for 0, 1 and 2 hours. 2 × 104 cells were incubated with Amplex Red reaction mixture and 10-7 M fMLP. Hydrogen peroxide production was measured using fluorimetric reader, and expressed in μM. Data represent mean ± SD of 7 separate experiments. *P = 0.015Back to article page