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.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 991-999 |
| Number of pages | 9 |
| Journal | EMBO Reports |
| Volume | 15 |
| Issue number | 9 |
| DOIs | |
| State | Published - Sep 2014 |
Keywords
- Ikaros
- NFAT
- regulatory T cell
ASJC Scopus subject areas
- Biochemistry
- Molecular Biology
- Genetics
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