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Immunity. 2010 Dec 14;33(6):890-904. doi: 10.1016/j.immuni.2010.12.002.

Foxo transcription factors control regulatory T cell development and function.

Author information

1
Molecular Biology Section, Division of Biological Sciences and Department of Cellular and Molecular Medicine, University of California, San Diego, La Jolla, CA 92093-0377, USA.

Erratum in

  • Immunity. 2011 Jan 28;34(1):135. Beisner, Daniel L [corrected to Beisner, Daniel R].

Abstract

Foxo transcription factors integrate extrinsic signals to regulate cell division, differentiation and survival, and specific functions of lymphoid and myeloid cells. Here, we showed the absence of Foxo1 severely curtailed the development of Foxp3(+) regulatory T (Treg) cells and those that developed were nonfunctional in vivo. The loss of function included diminished CTLA-4 receptor expression as the Ctla4 gene was a direct target of Foxo1. T cell-specific loss of Foxo1 resulted in exocrine pancreatitis, hind limb paralysis, multiorgan lymphocyte infiltration, anti-nuclear antibodies and expanded germinal centers. Foxo-mediated control over Treg cell specification was further revealed by the inability of TGF-β cytokine to suppress T-bet transcription factor in the absence of Foxo1, resulting in IFN-γ secretion. In addition, the absence of Foxo3 exacerbated the effects of the loss of Foxo1. Thus, Foxo transcription factors guide the contingencies of T cell differentiation and the specific functions of effector cell populations.

Comment in

PMID:
21167754
PMCID:
PMC3034255
DOI:
10.1016/j.immuni.2010.12.002
[Indexed for MEDLINE]
Free PMC Article

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