Thymic dendritic cell-derived IL-27p28 promotes the establishment of functional bias against IFN-γ production in newly generated CD4+ T cells through STAT1-related epigenetic mechanisms

The newly generated CD4 single-positive (SP) T lymphocytes are featured by enhanced IL-4 but repressed IFN-γ production. The mechanisms underlying this functional bias remain elusive. Previous studies have reported that CD4+ T cells from mice harboring DC-specific deletion of IL-27p28 display an increased capacity of IFN-γ production upon TCR stimulation. Here we demonstrated that similarly altered functionality occurred in CD4SP thymocytes, recent thymic emigrants (RTEs) as well as naive T cells from either Cd11c-p28f/f mice or mice deficient in the α subunit of IL-27 receptor. Therefore, DC-derived IL-27p28-triggered, IL-27Rα-mediated signal is critically involved in the establishment of functional bias against IFN-γ production during their development in the thymus. Epigenetic analyses indicated reduced DNA methylation of the Ifng locus and increased trimethylation of H3K4 at both Ifng and Tbx21 loci in CD4SP thymcoytes from Cd11c-p28f/f mice. Transcriptome profiling demonstrated that Il27p28 ablation resulted in coordinated up-regulation of STAT1-activated genes. Concurrently, STAT1 was found to be constitutively activated. Moreover, we observed increased accumulation of STAT1 at the Ifng and Tbx21 loci and a strong correlation between STAT1 binding and H3K4me3 modification of these loci. Of note, Il27p28 deficiency exacerbated the autoimmune phenotype of Aire-/- mice. Collectively, this study reveals a novel mechanism underlying the functional bias of newly generated CD4+ T cells and the potential relevance of such a bias in autoimmunity. ![Figure][1] ### Competing Interest Statement The authors have declared no competing interest. * AS : ankylosing spondyliti BD : behcet disease ChIP : chromatin immunoprecipitation cKO : conditional knockout DC : dendritic cell DEGs : differentially expressed genes EAE : experimental autoimmune encephalomyelitis EBI3 : Epstein-Barr virus-induced gene 3 ELISA : Enzyme-Linked Immunosorbent Assay GO : gene ontology GSEA : gene set enrichment analysis H3K4me3 : histone H3 lysine 4 trimethylation H3K27me3 : histone H3 lysine 27 trimethylation H3K9me3 : histone H3 lysine 9 trimethylation IFN-γ : interferon-γ IL-2 : interleukin 2 KEGG : Kyoto Encyclopedia of Genes and Genomes PBS : phosphate-buffered saline RTE : recent thymic emigrants SOCS3 : suppressors of cytokine signaling 3 SP : single-positive thymocyte STAT : signal transducer and activator of transcription T-bet : T-box transcription factor Th : T helper TNF-α : tumor necrosis factor α WT : wild-type. [1]: pending:yes