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Eur J Immunol. 2014 Jul;44(7):2074-84. doi: 10.1002/eji.201344072. Epub 2014 May 19.

NK cells gain higher IFN-γ competence during terminal differentiation.

Author information

1
Innate Immunity, Deutsches Rheuma-Forschungszentrum, A Leibniz Institute, Berlin, Germany.

Abstract

NK cells are the main cells of the innate immune system that produce IFN-γ, and they express this cytokine at early stages of maturation in response to cytokine stimulation. Conversely, acquisition of IFN-γ-competence in CD4(+) T helper cells requires a differentiation process from naïve toward type 1 (Th1) cells, which is associated with epigenetic remodeling at the IFNG locus. In the present study, we show that the ability of NK cells to produce IFN-γ in response to activating receptor (actR) engagement is gradually acquired during terminal differentiation and is accompanied by progressively higher NF-κB activation in response to actR triggering. Moreover, during the differentiation process NK cells gradually display increasing expression of IFNG and TBX21 (encoding T-bet) transcripts and demethylation at the IFNG promoter. This study provides new insights in the molecular mechanisms underlying NK-cell ability to express IFN-γ upon actR engagement. Thus, we propose that in order to efficiently produce IFN-γ in response to infected or transformed cells, NK cells gain Th1-like features, such as higher IFN-γ competence and epigenetic remodeling of the IFNG promoter, during their terminal differentiation.

KEYWORDS:

Cell differentiation; Chromatin remodeling; IFN-γ; NK cells

PMID:
24752800
DOI:
10.1002/eji.201344072
[Indexed for MEDLINE]
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