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Regulatory T cells suppress CD4+ T cells through NFAT-dependent transcriptional mechanisms.


ABSTRACT: Regulatory T cells (Tregs) control autoreactive T cells by inhibiting activation-induced proliferation and cytokine expression. The molecular mechanisms responsible for the inactivation of effector T cells by Tregs remain yet to be fully characterized. We report that T-helper cells stimulated in the presence of Tregs quickly activate NFAT1 and have increased NFAT1-dependent expression of the transcription repressor Ikaros. NFAT1 deficiency or dominant-negative Ikaros compromises Treg-mediated inhibition of T-helper cells in vitro and in vivo. Thus, our results place NFAT-dependent mechanisms as general regulators of T-cell tolerance and show that Treg-mediated suppression of T-helper cells results from the activation of NFAT-regulated gene expression.

SUBMITTER: Shin DS 

PROVIDER: S-EPMC4198043 | biostudies-literature | 2014 Sep

REPOSITORIES: biostudies-literature

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Regulatory T cells suppress CD4+ T cells through NFAT-dependent transcriptional mechanisms.

Shin Daniel S DS   Jordan Ayana A   Basu Samik S   Thomas Rajan M RM   Bandyopadhyay Sanmay S   de Zoeten Edwin F EF   Wells Andrew D AD   Macian Fernando F  

EMBO reports 20140729 9


Regulatory T cells (Tregs) control autoreactive T cells by inhibiting activation-induced proliferation and cytokine expression. The molecular mechanisms responsible for the inactivation of effector T cells by Tregs remain yet to be fully characterized. We report that T-helper cells stimulated in the presence of Tregs quickly activate NFAT1 and have increased NFAT1-dependent expression of the transcription repressor Ikaros. NFAT1 deficiency or dominant-negative Ikaros compromises Treg-mediated in  ...[more]

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