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. 2014 May 15;2014:257930. doi: 10.1155/2014/257930

Figure 2.

Figure 2

HMGB1-stimulated BMDCs induce IL-17A production and Th17 differentiation via IL-23 in vitro. (a) HMGB1-induced IL-23 expression in BMDCs. BMDCs were stimulated with graded concentrations of HMGB1 or culture medium for 2 d or stimulated with 500 ng/mL HMGB1 for the indicated times. The IL-23 levels in the cell culture supernatants were measured using ELISA. The values represent the means ± standard deviations (n = 5). **P < 0.01 compared with the medium control. (b and c) HMGB1-stimulated BMDCs modulate Th17 polarization. Activated, autologous CD4+ T cells (1 × 105) were cultured alone or cocultured with BMDCs (2.5 × 104) that were treated with or without 500 ng/mL HMGB1 in the presence or absence of IL-23p19 Ab or control IgG for 5 d, the culture supernatants were analyzed for IL-17A using ELISA (b), and the expression of intracellular IL-17 by CD4+ T cells was analyzed using FACS (c). The values represent the means ± standard deviations (n = 5). **P < 0.01 compared with the HMGB1-DC group.