RORγt expression in mature TH17 cells safeguards their lineage specification by inhibiting conversion to TH2 cells.
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ABSTRACT: RORγt is the lineage-specific transcription factor for T helper 17 (TH17) cells and an attractive drug target for treating TH17-associated diseases. Although the critical role of RORγt in early TH17 cell differentiation has been well recognized, its function in mature TH17 cell maintenance remains largely unknown. Here, we show that genetic deletion of Rorc in mature TH17 cells inhibited their pathogenic functions. Mechanistically, loss of RORγt led to a closed chromatin configuration at key TH17-specific gene loci, particularly at the "super-enhancer" regions. Unexpectedly, RORγt directly bound and inhibited Il4 transcription, whereas pharmaceutically or genetically targeting RORγt caused spontaneous conversio
SUBMITTER: Chi X
PROVIDER: S-EPMC9417185 | biostudies-literature | 2022 Aug
REPOSITORIES: biostudies-literature
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