Figure 7.
Figure 7. Nonpersistent ERK1/2 phosphorylation in CD1c+ PBDCs and migratory MoDCs activated with CD40L3 plus IFN-γ. CD1c+ PBDCs were isolated from PBMCs. Following a 24-hour culture in the presence of GM-CSF plus IL-4, CD1c+ PBDCs (5 × 105 per condition) were stimulated with CD40L3 plus IFN-γ for 30 minutes or 24 hours. Subsequently, CD1c+ PBDCs were harvested, washed, resuspended at concentrations of 5 × 106/mL in Western sample buffer, and snap frozen. ERK1/2 phosphorylation of 1 representative experiment is shown (n = 3 for CD1c+ PBDCs). Immature MoDCs were stimulated with CD40L3 plus IFN-γ directly following the 7-day culture period (n = 5). Migratory MoDCs were initially stimulated with GM-CSF plus TNF-α plus IFN-α plus PGE2 for 24 hours and then washed, and CD40L3 plus IFN-γ was added as indicated (n = 4).

Nonpersistent ERK1/2 phosphorylation in CD1c+PBDCs and migratory MoDCs activated with CD40L3plus IFN-γ. CD1c+ PBDCs were isolated from PBMCs. Following a 24-hour culture in the presence of GM-CSF plus IL-4, CD1c+ PBDCs (5 × 105 per condition) were stimulated with CD40L3 plus IFN-γ for 30 minutes or 24 hours. Subsequently, CD1c+ PBDCs were harvested, washed, resuspended at concentrations of 5 × 106/mL in Western sample buffer, and snap frozen. ERK1/2 phosphorylation of 1 representative experiment is shown (n = 3 for CD1c+ PBDCs). Immature MoDCs were stimulated with CD40L3 plus IFN-γ directly following the 7-day culture period (n = 5). Migratory MoDCs were initially stimulated with GM-CSF plus TNF-α plus IFN-α plus PGE2 for 24 hours and then washed, and CD40L3 plus IFN-γ was added as indicated (n = 4).

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