Fig. 3.
LPS and THP-1 showed different immune induction patterns in different time spans. A THP-1 was treated with 0, 0.01, 0.1, 1 μg/mL LPS, and total RNA was collected at 3, 6, 12, 24, 48, and 96 h. IL-6 and IL-8 mRNA expressions were determined by RT-qPCR. IL-6 was up-regulated in all LPS-treated THP-1 cells. IL-8 was up-regulated by LPS at 3–12 h, and this induction was decreased after 12 h. The data were expressed as the mean ± SD of triplicates from three independent experiments. ***, p < 0.0005 compared with LPS 0 μg/mL group; ###, p < 0.0005 compared with LPS 0.01 μg/mL group; ΨΨ, p < 0.005 compare with LPS 0.1 μg/mL group. Two-way ANOVA. B DPCs were treated with 0, 0.01, 0.1, 1 μg/mL LPS, and total RNA was collected at 3, 6, 12, 24, 48, and 96 h. IL-6 and IL-8 mRNA expression was determined by RT-qPCR. IL-6 was up-regulated by LPS at 6 h, and this induction was decreased after 6 h. IL-8 was up-regulated by LPS at 6 and 12 h, and this induction was decreased after 12 h. The data were expressed as the mean ± SD of triplicates from three independent experiments. **, p < 0.005; ***, p < 0.0005 compared with LPS 0 μg/mL group; #, p < 0.05; ##, p < 0.005 compare with LPS 0.01 μg/mL group; ns, no significance; Ψ, p < 0.05 compare with LPS 0.1 μg/mL group. Two-way ANOVA. C DPCs were cocultured with different ratios of THP-1 cells, and total RNA was collected at 3, 6, 12, 24, 48, and 96 h. IL-6 and IL-8 mRNA expressions were determined by RT-qPCR. IL-6 and IL-8 were up-regulated after 12 h, and the induction effects were decreased after 48 h. Furthermore, THP-1: DPCs = 1:2 could continuously induce IL-8 expressions after 48 h. The data were expressed as the mean ± SD of triplicates from three independent experiments. ***, p < 0.0005 compared with THP-1:DPCs = 0:1; ###, p < 0.0005 compared with THP-1: DPCs = 1:10. Two-way ANOVA
