Figure 1.
Figure 1. PDCs contribute to B-cell activation within PBMCs. Cells were incubated with CpG-C (3 μg/mL), anti-Ig (10 μg/mL), or a combination of CpG-C and anti-Ig. After 72 hours CD86 was analyzed on CD19+ B cells by flow cytometry. Data are presented as mean fluorescence intensity (MFI ±SEM). (A) Total PBMCs (▪) or PBMCs depleted of PDCs (▨) were used (n = 4 independent experiments). (B) Isolated B cells were incubated alone (1 × 105 B cells/200 μL/well) or cocultured with PDCs (1 × 104 PDC/200 μL/well; n = 5 independent experiments; □, B cells alone; ▪, B cells and PDCs).

PDCs contribute to B-cell activation within PBMCs. Cells were incubated with CpG-C (3 μg/mL), anti-Ig (10 μg/mL), or a combination of CpG-C and anti-Ig. After 72 hours CD86 was analyzed on CD19+ B cells by flow cytometry. Data are presented as mean fluorescence intensity (MFI ±SEM). (A) Total PBMCs (▪) or PBMCs depleted of PDCs (▨) were used (n = 4 independent experiments). (B) Isolated B cells were incubated alone (1 × 105 B cells/200 μL/well) or cocultured with PDCs (1 × 104 PDC/200 μL/well; n = 5 independent experiments; □, B cells alone; ▪, B cells and PDCs).

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