Figure 5.
Figure 5. Increased Ag uptake of BM-DCs from ICSBP–/– mice. BM-DCs of ICSBP–/– and WT mice were cultured for 6 days in the presence of GM-CSF. (A) Cells were then incubated for 40 minutes with 1 mg/mL DX-FITC and then stained for CD11c and CD86 expression. Density plots represent the uptake of the DX and the relative expression of CD86 in a population gated on forward–side scatter properties and on CD11c positivity. Data are representative of 3 separate experiments. (B) qRT-PCR analysis of mannose receptor (Mrc1) transcript levels in BM-DCs at different times of culture. Total RNA was extracted from ICSBP–/– and WT BM-DCs at the indicated time points and used to generate cDNA that was analyzed by qRT-PCR. The cDNA concentrations were normalized to β-actin expression. The fold changes of Mrc1 transcripts of WT (•) and ICSBP–/– BM-DCs (○) are expressed relative to 0 days using the ΔΔCT method (“Materials and methods”). Results are representative of 3 separate experiments.

Increased Ag uptake of BM-DCs from ICSBP–/– mice. BM-DCs of ICSBP–/– and WT mice were cultured for 6 days in the presence of GM-CSF. (A) Cells were then incubated for 40 minutes with 1 mg/mL DX-FITC and then stained for CD11c and CD86 expression. Density plots represent the uptake of the DX and the relative expression of CD86 in a population gated on forward–side scatter properties and on CD11c positivity. Data are representative of 3 separate experiments. (B) qRT-PCR analysis of mannose receptor (Mrc1) transcript levels in BM-DCs at different times of culture. Total RNA was extracted from ICSBP–/– and WT BM-DCs at the indicated time points and used to generate cDNA that was analyzed by qRT-PCR. The cDNA concentrations were normalized to β-actin expression. The fold changes of Mrc1 transcripts of WT (•) and ICSBP–/– BM-DCs (○) are expressed relative to 0 days using the ΔΔCT method (“Materials and methods”). Results are representative of 3 separate experiments.

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