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. 2021 Sep 23;218(11):e20210021. doi: 10.1084/jem.20210021

Figure 1.

Figure 1.

Cell-intrinsic role of IL-27 in promoting CD8αα+CD4+ IEL differentiation. (A) Frequencies of small intestinal CD8αα+CD4+ IELs in naive WT mice over time. (B–D) Representative FACS profiles with gating strategy for different IEL subsets (B) and frequencies of CD8α+ in TCRβ+TCRγδCD4+ cells (C) and TCRβ+TCRγδCD8α+CD4+ cells (D) in total IELs from young (∼10–12 wk) T-rKO mice and WT littermates. (E–J) Representative FACS profiles with gating strategy for different IEL subsets (E) and frequencies of CD8α+ in TCRβ+TCRγδCD4+ cells (F) and TCRβ+TCRγδCD8α+CD4+ in total IELs (G), as well as frequencies of TCRαβ+CD8αβ+(H), TCRαβ+CD8αα+ (I), and TCRγδ+CD8αα+ (J) IEL subsets from old (>6 mo) T-rKO mice and WT littermates. Each symbol represents an individual mouse, and the bar represents the mean. Data are pooled from at least three independent experiments. Results of Student’s t test: ***, P < 0.001.