Bcl11b prevents fatal autoimmunity by promoting Treg cell program and constraining innate lineages in Treg cells.
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ABSTRACT: Regulatory T (Treg) cells are essential for peripheral tolerance and rely on the transcription factor (TF) Foxp3 for their generation and function. Several other TFs are critical for the Treg cell program. We found that mice deficient in Bcl11b TF solely in Treg cells developed fatal autoimmunity, and Bcl11b-deficient Treg cells had severely altered function. Bcl11b KO Treg cells showed decreased functional marker levels in homeostatic conditions, inflammation, and tumors. Bcl11b controlled expression of essential Treg program genes at steady state and in inflammation. Bcl11b bound to genomic regulatory regions of Treg program genes in both human and mouse Treg cells, overlapping with Foxp3 binding; the
SUBMITTER: Drashansky TT
PROVIDER: S-EPMC6685710 | biostudies-literature | 2019 Aug
REPOSITORIES: biostudies-literature
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