Figure 7.
Figure 7. Differential cytokine production in 2 subsets of pDCs. (A-D) After depletion of CD3+, CD19+, CD11b+, and DX5+ cells from BALB/c bone marrow, cells were stained with B220, CD11c, and 2E6 Abs. The 2E6+ (▪) or 2E6– (▦) cells were sorted within the gate of B220+CD11c+ cells and then 4 × 104 cells/well of each group were plated onto 96-well round-bottom plates. These cells were variously stimulated (influenza virus PR8, CpG-ODN, or HSV) at 37°C for 24 hours, then supernatants of IFN-α, TNF-α, IL-6, and IL-12p70 were measured by ELISA. Experiments were performed at least 3 times with similar results. Values represent the mean ± SD from triplicate samples. (E) 2E6– pDCs acquire the expression of Ly49Q. Sorted 2E6– pDCs derived from bone marrow were cultured in the presence of Flt-3L (100 ng/mL) for 0, 2, and 4 days. Cells were then stained with 2E6 mAb and analyzed by FACS.

Differential cytokine production in 2 subsets of pDCs. (A-D) After depletion of CD3+, CD19+, CD11b+, and DX5+ cells from BALB/c bone marrow, cells were stained with B220, CD11c, and 2E6 Abs. The 2E6+ (▪) or 2E6 (▦) cells were sorted within the gate of B220+CD11c+ cells and then 4 × 104 cells/well of each group were plated onto 96-well round-bottom plates. These cells were variously stimulated (influenza virus PR8, CpG-ODN, or HSV) at 37°C for 24 hours, then supernatants of IFN-α, TNF-α, IL-6, and IL-12p70 were measured by ELISA. Experiments were performed at least 3 times with similar results. Values represent the mean ± SD from triplicate samples. (E) 2E6 pDCs acquire the expression of Ly49Q. Sorted 2E6 pDCs derived from bone marrow were cultured in the presence of Flt-3L (100 ng/mL) for 0, 2, and 4 days. Cells were then stained with 2E6 mAb and analyzed by FACS.

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