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. 2019 Mar 14;10:441. doi: 10.3389/fimmu.2019.00441

Figure 4.

Figure 4

PDC in hepatic and inguinal lymph nodes, spleen and liver. (A) Flowcytometric determination of PDC in MNC isolated from hepatic and inguinal lymph nodes, spleen, and liver perfusate using anti-BDCA2 and anti-BDCA4 antibodies. Non-hematopoietic cells and dead cells were excluded from the analysis by exclusion of CD45 cells and 7-AAD+ cells. (B) Percentages of BDCA2+BDCA4+ PDC within MNC in the different tissues. Dots represent data from individual tissues and lines indicate mean values. (C) Histograms showing HLA-DR and CD40 expression on PDC from the different tissues. Light gray histograms are isotype control stains. (D) Summary of the expression levels of HLA-DR and CD40 on PDC in hepatic (H) lymph nodes (n = 6) and inguinal lymph nodes (n = 7), spleen (n = 6), and liver (n = 6). Data are depicted as means with SEM. No significant differences were observed (E) Graded numbers of purified hepatic (n = 6) and inguinal LN PDC (n = 5) were co-cultured with allogeneic T-cells (from one batch) and T-cell proliferation was assessed after 5 days by [3H]-thymidine incorporation. T-cell proliferation in response to PHA is depicted as positive control condition. Data represent means with SEM. No significant differences were observed.