Figure 1
Figure 1. Characterization of CCR9− and CCR9+ PDCs in murine bone marrow. Expression of the indicated markers was analyzed by FACS in primary BM cells. Dot plots show expression of CD11c versus BST2 in propidium iodide-negative cells and expression of BST2 versus CCR9 in BST2+ CD11c+ cells. Expression of the indicated markers in CCR9+ and CCR9− BST2+ CD11c+ cells is shown below (overlay with fluorescence minus one [FMO] control, filled histograms) (A). Relative mRNA expression was quantified in CCR9+/BST2+/CD11c+ and CCR9−/BST2+/CD11c+ PDC populations sorted from primary BM cells by quantitative RT-PCR (B, mean ± SD, n = 3). Immunoglobulin DH-JH rearrangement was detected by PCR in genomic DNA isolated from CCR9+ and CCR9− PDCs (C). CCR9+ and CCR9− PDCs were incubated with medium or CpG 2216 for 24 hours. IFN-α, IL-12p40, and IL-6 were measured in the supernatants by ELISA (D, mean ± SD, n = 3). *P < .05. **P < .01. ***P < .001. n.s. indicates not significant.

Characterization of CCR9 and CCR9+ PDCs in murine bone marrow. Expression of the indicated markers was analyzed by FACS in primary BM cells. Dot plots show expression of CD11c versus BST2 in propidium iodide-negative cells and expression of BST2 versus CCR9 in BST2+ CD11c+ cells. Expression of the indicated markers in CCR9+ and CCR9 BST2+ CD11c+ cells is shown below (overlay with fluorescence minus one [FMO] control, filled histograms) (A). Relative mRNA expression was quantified in CCR9+/BST2+/CD11c+ and CCR9/BST2+/CD11c+ PDC populations sorted from primary BM cells by quantitative RT-PCR (B, mean ± SD, n = 3). Immunoglobulin DH-JH rearrangement was detected by PCR in genomic DNA isolated from CCR9+ and CCR9 PDCs (C). CCR9+ and CCR9 PDCs were incubated with medium or CpG 2216 for 24 hours. IFN-α, IL-12p40, and IL-6 were measured in the supernatants by ELISA (D, mean ± SD, n = 3). *P < .05. **P < .01. ***P < .001. n.s. indicates not significant.

Close Modal

or Create an Account

Close Modal
Close Modal