TABLE 2.
iNOS, NO, and GSH levels in J774 cellsa
Infection and treatment | Nitrite production (nmol/mg of protein)b
|
Pc | iNOS level (% fluorescent)d | GSH level (nmol/mg of protein)e
|
Pc | ||
---|---|---|---|---|---|---|---|
Mean | SE | Mean | SE | ||||
No infection | 0.162 | 0.034 | 2.4 | 3.99 | 0.284 | ||
BCG | |||||||
None | 0.128 | 0.020 | 11.06 | 4.127 | 0.068 | ||
IFN-γ + LPS | 1.889 | 0.147 | 0.003 | 26.22 | 0.434 | 0.041 | 0.0127f |
DPP | |||||||
None | 0.136 | 0.018 | 6.82 | 3.93 | 0.585 | ||
IFN-γ + LPS | 2.241 | 0.041 | 0.0001 | 24.15 | 0.748 | 0.100 | 0.033f |
J774.1 cells were maintained in DMEM containing 10% fetal bovine serum. Macrophages were infected with mycobacteria at a 10:1 ratio and incubated for 2 h. Unphagocytosed organisms were removed by washing, and the infected macrophages were maintained in DMEM containing 10% fetal bovine serum or in medium containing IFN-γ (100 U/ml) and LPS (1 μg/ml). Infected macrophage cultures were terminated at 72 h to determine nitrite production and iNOS and GSH levels.
Determined by the Griess reaction.
Calculated with the Statview program.
iNOS levels were studied by immunocytochemical staining and analysed by flow cytometry.
Determined by spectrophotometry.
Compared with the value for untreated cells.