Epigenetic initiation of the T _H 17 differentiation program is promoted by Cxxc finger protein 1

Abstract

IL-6/STAT3 signaling is known to initiate the T_H17 differentiation program, but the upstream regulatory mechanisms remain minimally explored. Here, we show that Cxxc finger protein 1 (Cxxc1) promoted the generation of T_H17 cells as an epigenetic regulator and prevented their differentiation into T_reg cells. Mice with a T cell-specific deletion of Cxxc1 were protected from experimental autoimmune encephalomyelitis and were more susceptible to <i>Citrobacter rodentium</i> infection. Cxxc1 deficiency decreased IL-6Rα expression and impeded IL-6/STAT3 signaling, whereas the overexpression of IL-6Rα could partially reverse the defects in <i>Cxxc1</i>-deficient T_H17 cells in vitro and in vivo. Genome-wide occupancy analysis revealed that Cxxc1 bound to <i>Il6r</i>α gene loci by maintaining the appropriate H3K4me3 modification of its promoter. Therefore, these data highlight that Cxxc1 as a key regulator governs the balance between T_H17 and T_reg cells by controlling the expression of IL-6Rα, which affects IL-6/STAT3 signaling and has an impact on T_H17-related autoimmune diseases.