Fig. 5.
FITC dextran and HRP uptake by the two DC subpopulations is mediated through receptors for mannose polymers. The experiments of FITC dextran uptake were performed on day-6 CD1a precursors by double color fluorescence (A and C) and on day-11 CD14-derived DCs (B and D; see legend to Figs 3 and 4). The uptake of HRP was performed on day-6 and day-11 CD1a+- and CD14-derived cells (E and F ). (A and B) Cells were pulsed for 15 minutes at 37°C with various concentrations of FITC dextran in the absence or in the presence of 1 mg/mL mannan. (C and D) Cells were pulsed for various times at 37°C with 0.1 mg/mL FITC dextran in the absence or in the presence of 1 mg/mL mannan. (E and F ) Cells were pulsed for 15 minutes at 37°C with various concentrations of HRP in the absence or in the presence of 1 mg/mL mannan. Results of each panel are representative of three experiments or more.

FITC dextran and HRP uptake by the two DC subpopulations is mediated through receptors for mannose polymers. The experiments of FITC dextran uptake were performed on day-6 CD1a precursors by double color fluorescence (A and C) and on day-11 CD14-derived DCs (B and D; see legend to Figs 3 and 4). The uptake of HRP was performed on day-6 and day-11 CD1a+- and CD14-derived cells (E and F ). (A and B) Cells were pulsed for 15 minutes at 37°C with various concentrations of FITC dextran in the absence or in the presence of 1 mg/mL mannan. (C and D) Cells were pulsed for various times at 37°C with 0.1 mg/mL FITC dextran in the absence or in the presence of 1 mg/mL mannan. (E and F ) Cells were pulsed for 15 minutes at 37°C with various concentrations of HRP in the absence or in the presence of 1 mg/mL mannan. Results of each panel are representative of three experiments or more.

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