Tissue-specific emergence of regulatory and intraepithelial T cells from a clonal T cell precursor.
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ABSTRACT: Peripheral Foxp3+ regulatory T cells (pTregs) maintain immune homeostasis by controlling potentially harmful effector T cell responses toward dietary and microbial antigens. Although the identity of the T cell receptor (TCR) can impose commitment and functional specialization of T cells, less is known about how TCR identity governs pTreg development from conventional CD4+ T cells. To investigate the extent to which TCR identity dictates pTreg fate, we used somatic cell nuclear transfer to generate a transnuclear (TN) mouse carrying a monoclonal TCR from a pTreg (pTreg TN mice). We found that the pTreg TCR did not inevitably predispose T cells to become pTreg but instead allowed for differenti
SUBMITTER: Bilate AM
PROVIDER: S-EPMC6296461 | biostudies-literature | 2016 Aug
REPOSITORIES: biostudies-literature
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