TABLE 2.
Effects of BDM on PMN oxidative burst and fMLP binding after IL-18 activation
BDM concn (mM) | Mean fluorescence intensity of:
|
|||
---|---|---|---|---|
E+ contenta
|
FITC-fMLPb
|
|||
PBS | IL-18 + fMLP | PBS | IL-18 | |
0 | 15.8 ± 1.0 | 43.5 ± 5.6c | 58.3 ± 1.9 | 43.7 ± 1.3c |
0.1 | 13.0 ± 1.0 | 59.0 ± 1.0c,d | 56.0 ± 1.5 | 40.0 ± 3.2c,d |
1 | 15.0 ± 0.6 | 67.3 ± 6.2c,d | 54.7 ± 1.7 | 33.0 ± 3.5c,d |
5 | 15.5 ± 1.3 | 26.8 ± 3.5 | 55.7 ± 5.2 | 44.0 ± 5.7 |
10 | 15.5 ± 0.6 | 20.5 ± 3.1 | 55.0 ± 3.5 | 47.3 ± 4.9 |
Samples were preincubated at 37°C with BDM at various concentrations for 5 min before the addition of hydroethidine for 15 min; the samples were then exposed to IL-18 (500 ng/ml) for 45 min and stimulated with fMLP (10−6 M) for 5 min. The mean fluorescence intensity of E+ was recorded as described in Materials and Methods. Values are expressed as means ± SEMs (n = 3).
Samples were preincubated for 20 min at 37°C with BDM at various concentrations and were then exposed to IL-18 (500 ng/ml) for 45 min. The mean fluorescence intensity of FITC-fMLP was recorded as described in Materials and Methods. Values are expressed as means ± SEMs (n = 3).
Significantly different from the results for the samples incubated with PBS instead of IL-18.
Significantly different from the results for the samples incubated with PBS instead of BDM.