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. 2019 Sep 28;8(12):e1665975. doi: 10.1080/2162402X.2019.1665975

Figure 2.

Figure 2.

Post-ETBF myeloid cell subset kinetics and function.

Panel a. CD11b+ myeloid cell subset kinetics in the colon. LP CD11b+CX3CR1+ and CD11b+CX3CR1 myeloid cell numbers were quantified in post-ETBF mice. Error bars = SEM, n = 3-6/time point. Days 2–6 were significantly different than day 0 (p < .05). Panel b. In vitro co-culture assay. Sorted CD11b+ cell subsets were incubated with CD4+ T-cells as described in the Methods. Control T-cells were isolated from naïve APCmin/+ mice whereas experimental T-cells (Bf) were purified from ETBF-inoculated mice. Representative FACS panels are shown for control (T-cells only, top row) and experimental (T-cells + myeloid cells, bottom row). CD4+ T-cells were gated on and analyzed for Foxp3 vs IL-17 production. Quantitative data are shown for percent Foxp3+ and IL-17+ cells for each well. Error bars = SEM, n = 3 mice per group (** and *** denote p < .01 and < 0.001, respectively). Data from one of two repeats with similar results are shown.