Fig. 6.
Fig. 6. IL-3 or forskolin stimulated phosphorylation of CREB occurs independently of p38 MAPK and MAPKAP kinase-2. (A) MC/9 cells were treated with SB203580 (1 μmol/L) or vehicle alone for 20 minutes, followed by treatments with either 10 μg/mL synthetic IL-3, 50 μmol/L C2-ceramide, or both, for 5 minutes. Whole-cell lysates were separated on SDS-PAGE and immunoblot analysis was performed to detect phospho-CREB. (B) MC/9 cells were treated with 10 μg/mL synthetic IL-3 for the times indicated following pretreatment with SB203580 or vehicle alone for 20 minutes. Immunoblot analysis was performed to detect phospho-CREB (top) and CREB (bottom). (C) MC/9 cells were treated with 10 μg/mL IL-3 for the times indicated, following treatment with SB203580 (1 μmol/L) or vehicle alone for 20 minutes. Lysates were incubated with 1 μg anti-MAPKAP kinase-2 antibody and protein G-Sepharose beads, and kinase activity was determined from the washed immunoprecipitates by measuring the32P transferred to Hsp25. (D) Cells were treated with the indicated concentrations of forskolin for 10 minutes following a 20-minute treatment with SB203580 (1 μmol/L) or vehicle alone. Immunoblot analysis was performed to detect phospho-CREB (top) and CREB (bottom).

IL-3 or forskolin stimulated phosphorylation of CREB occurs independently of p38 MAPK and MAPKAP kinase-2. (A) MC/9 cells were treated with SB203580 (1 μmol/L) or vehicle alone for 20 minutes, followed by treatments with either 10 μg/mL synthetic IL-3, 50 μmol/L C2-ceramide, or both, for 5 minutes. Whole-cell lysates were separated on SDS-PAGE and immunoblot analysis was performed to detect phospho-CREB. (B) MC/9 cells were treated with 10 μg/mL synthetic IL-3 for the times indicated following pretreatment with SB203580 or vehicle alone for 20 minutes. Immunoblot analysis was performed to detect phospho-CREB (top) and CREB (bottom). (C) MC/9 cells were treated with 10 μg/mL IL-3 for the times indicated, following treatment with SB203580 (1 μmol/L) or vehicle alone for 20 minutes. Lysates were incubated with 1 μg anti-MAPKAP kinase-2 antibody and protein G-Sepharose beads, and kinase activity was determined from the washed immunoprecipitates by measuring the32P transferred to Hsp25. (D) Cells were treated with the indicated concentrations of forskolin for 10 minutes following a 20-minute treatment with SB203580 (1 μmol/L) or vehicle alone. Immunoblot analysis was performed to detect phospho-CREB (top) and CREB (bottom).

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