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. 2022 Nov 25;15(3):613–632. doi: 10.1016/j.jcmgh.2022.11.005

Figure 3.

Figure 3

Isolated KLPJ induces colitis in pan-antibiotics–treated mice. (A) Schematic of the experiment for KLPJ-induced colitis. (B) Body weights of mice (n = 9). (C) Colon length in mice (n = 6). (D) ELISA of tumor necrosis factor α (TNFα), IL6, and IL18 in the colon tissues of mice (n = 6). (E) CFU of KLPJ or E coli in the colon contents of mice. For CFU in the bacteria-infused mice, 109 bacteria were orally infused and then CFU were counted after 7 days. (F) Flow cytometry of CD11b+Ly6G+ cells in the colon tissues of mice (n = 5). Control indicates Ly6G isotypic control. (G) Flow cytometry of CD4+IFNγ+ cells in the colon tissues of mice (n = 5). Control indicates IFNγ isotypic control. (H) Flow cytometry of NKp46+IFNγ+ cells in the colon tissues of mice (n = 5). Control indicates isotypic control. (I) Flow cytometry of CD11b+MHCII+Ly6C+ inflammatory macrophages in the colon tissues of mice (n = 5). Control indicates isotypic control. Mice with (KLPJ or E coli) or without (PBS) gavage of KLPJ or E coli; PBS indicates control. (B) One-way analysis of variance test; (C–I), Student t test. ∗∗P < .01 and ∗∗∗P < .001. Data are representative of at least 2 experiments. FITC, fluorescein isothiocyanate; SSC,SideScatter.