Figure 2
Figure 2. Superoxide in bone marrow PMNs from BK+/+ and BK−/− mice. Net superoxide production as well as the kinetics over 60 minutes by PMA-stimulated PMNs was the same in normal and BK−/− mice (A). The BK channel inhibitor IbTX had no effect on extracellular superoxide generation by either PMN population (B). Superoxide generation after opsonized zymosan was the same in BK+/+ and BK−/− cells (C). Intracellular NADPH oxidase activity, assessed as the DHR oxidation by stimulated PMNs measured and quantitated as mean fluorescent intensity (MFI), was the same in BK+/+ and BK−/− cells (D) based on the light scatter characteristics (E). PMNs specific GR-1 staining in whole blood indicated that the gated populations used to assess DHR oxidation were indeed PMNs (F).

Superoxide in bone marrow PMNs from BK+/+ and BK−/− mice. Net superoxide production as well as the kinetics over 60 minutes by PMA-stimulated PMNs was the same in normal and BK−/− mice (A). The BK channel inhibitor IbTX had no effect on extracellular superoxide generation by either PMN population (B). Superoxide generation after opsonized zymosan was the same in BK+/+ and BK−/− cells (C). Intracellular NADPH oxidase activity, assessed as the DHR oxidation by stimulated PMNs measured and quantitated as mean fluorescent intensity (MFI), was the same in BK+/+ and BK−/− cells (D) based on the light scatter characteristics (E). PMNs specific GR-1 staining in whole blood indicated that the gated populations used to assess DHR oxidation were indeed PMNs (F).

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