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. 2018 May 3;9:1779. doi: 10.1038/s41467-018-03670-6

Fig. 5.

Fig. 5

Wild-type M2r macrophage protect Was−/−Rag−/− mice from T-cell-transfer-induced colitis. Was−/−Rag1−/− mice were transfer with PBS (n = 9), WT M2r (2 × 106) (n = 9) or Was−/− M2r (2 × 106) (n = 7) macrophages one-day before WT CD4+ T-cell transfer. As a control Rag1−/− (n = 7) were treated with PBS and transferred with WT CD4+ T cells. a Mean ± SEM % initial body weight after T-cell transfer. Data are cumulative of two independent experiments. **p < 0.01, ***p < 0.001 (two-way ANOVA) (Was−/−Rag1−/− tx PBS Vs Was−/−Rag1−/− tx WT M2r). b Representative photomicrographs of H&E stained colonic section and histological score. Scale bars: 200 μm. c Absolute number and frequency of cytokine producing helper T cells in the LP was determined by flow cytometry. (Rag1−/− tx PBS n = 5; Was−/−Rag1−/− tx PBS n = 5; Was−/−Rag1−/− tx WT M2r n = 5; Was−/−Rag1−/− tx Was−/− M2r n = 5). Data are cumulative of two independent experiments. Data shown in b,c are mean ± SEM and P-value was obtained by Student’s t-test. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001; NS, not significant; tx: treated