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Fig. 8 | Journal of Neuroinflammation

Fig. 8

From: GPR43 stimulation on TCRαβ+ intraepithelial colonic lymphocytes inhibits the recruitment of encephalitogenic T-cells into the central nervous system and attenuates the development of autoimmunity

Fig. 8

Pharmacologic stimulation of GPR43 on IEL induces an anti-inflammatory effect in experimental colitis. Inflammatory colitis was induced in Rag1−/− Cd45.2+/+ mice by the i.v. transference of 5 × 105 naïve CD45.1+CD45.2+ CD4+ T-cells. In addition, some groups of mice received 5 × 105 of IEL treated with 4-CMTB (blue) or untreated (UT black). As a control, another group received only total CD45.1+CD45.2+ CD4+ T-cells (grey). A Schematic illustration of the experimental design. B Body weight was weekly registered throughout the whole time and the percentage of body weight change relative to the initial weight was quantified. Values represent mean ± SEM. C At week 6, mice were sacrificed and the colon length was assessed. Each symbol represents data obtained from an individual mouse. D MNC were isolated from the colonic lamina propria 6 weeks after the transfer and the percentage of infiltration of each population was determined by flow cytometry: therapeutic IEL (CD45.1+), donor CD4+ T-cells (CD45.1+ CD45.2+), Total TCRβ+ T-cells (CD45.1+TCRβ+); Total innate CD45+ cells (CD45+TCRβ) and total leukocytes (CD45+). BD Mean ± SEM from 4 to 7 mice per group. *, p < 0.05; **, p < 0.01; ***, p < 0.001 by one-way ANOVA followed by Dunnett’s post-hoc test (B, comparing different experimental groups in each single day), or by Tukey’s post-hoc test (C and D). B Black asterisks correspond to comparisons between Tn + IEL UT and Total CD4+, whilst red asterisks correspond to comparisons between Tn and Total CD4+ groups

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