T cell factor 1 (Tcf1) promotes the central memory CD8 T (T) cell differentiation and stemness in lymphoid tissues after systemic infections. It remains unclear whether Tcf1 regulates the CD103 tissue-resident memory CD8 T (T) cell formation in non-lymphoid tissues after mucosal infections. We find that Tcf1 is progressively decreased during lung T cell formation. Abrogation of transforming growth factor β (TGF-β) signaling is associated with a loss of CD103 and reciprocal gain of Tcf1 cells among T precursors in vivo. T-cell-specific ablation of Tcf7 enhances CD103 protein expression in T cells and precursors and increases T cell numbers after primary and secondary infections. Tcf1 directly binds to the Itgae (encoding CD103) locus and partly inhibits TGF-β-induced CD103 expression. Our study suggests that memory T cell tissue residency and homeostatic proliferation are reciprocally regulated by Tcf1. Tcf1 may play either immunosupportive or immunosuppressive roles in CD8 T cells, depending on systemic or mucosal infections.
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http://dx.doi.org/10.1016/j.celrep.2020.03.048 | DOI Listing |
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