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. 2018 Dec 14;9:2954. doi: 10.3389/fimmu.2018.02954

Figure 3.

Figure 3

Deficiency in CD4-intrinsic mPGES-1 impairs Teff CD4+ cell expansion but enhances Treg localization and RORγt expression in the colonic lamina propria. (A,B) Rag1−/− recipient mice received a co-transfer of a 1:1 mix of CD45.1+ WT (blue) and CD45.2+ mPGES-1−/− (red) Teff cells. Flow cytometric analysis of the (A) mLN and (B) cLP CD4+ populations, with representative dot plots indicating intracellular expression of CD45.1 or CD45.2 congenic marker expression together with RORγt. In the cLP plot (B), the shaded box indicates a unique RORγthi population of mPGES-1 deficient cells in the cLP. Graphs on the right indicate the proportions and total numbers for each group. (C) Co-transfer of either CD45.1+ WT Treg with CD45.2+ mPGES-1−/− Teff cells or CD45.2+ mPGES-1−−/− Treg cells with CD45.1+ WT Teff into Rag1−/− recipients. Transfers were always performed with a 2:1 Teff:Treg ratio. In the cLP, mPGES-1−/− CD4+ T cells are able to acquire higher RORγt expression than WT cells (shaded boxes). These CD4+RORγthi cells arise from both mPGES-1−/− Teff cells and mature Treg cells. Graphs on the bottom show the proportions of WT or mPGES-1−/− Treg cells that are either RORγt or RORγt+ in the mLN or the cLP. **P < 0.05 using in a one-way ANOVA with Welch's correction.