TABLE 3.
Effects of SB203580 and U0126 on intracellular IL-1α, IL-1β, IL-8, IL-1ra, and TNF-α production by SAC-stimulated monocytesa
| Treatment | % of cytokine-positive CD14+-gated monocytesb
|
||||
|---|---|---|---|---|---|
| IL-1α | IL-1β | IL-8 | IL-1ra | TNF-α | |
| RPMI | 2 | 0 | 12 | 2 | 0 |
| SAC | 37 | 77 | 70 | 21 | 78 |
| SAC + SB203580 | 54 | 89 | 39 | 15 | 92 |
| SAC + U0126 | 27 | 74 | 74 | 26 | 81 |
| SAC + SB203580 + U0126 | 18 | 68 | 71 | 22 | 87 |
a Purified human monocytes (106/ml) were cultured for 18 h at 37°C without or with SAC (100 μg/ml) and treated with 5 μM SB203580, with 10 μM U0126, or with a mixture of SB203580 and U0126. Intracellular cytokine production was detected using specific anti-cytokine-PE or anti-cytokine-APC MAbs. An isotypic control was used as a negative control. Monocytes were gated using either anti-CD14-FITC or anti-CD14-PE MAbs. At least 5,000 CD14+ events were acquired for intracellular cytokine analysis.
b Compared to isotypic negative controls. Results are those from one representative experiment out of three performed with cells from different donors.