Epigenetic Control of Interferon-Gamma Expression in CD8 T Cells

Author:

de Araújo-Souza Patrícia S.12,Hanschke Steffi C. H.1,Viola João P. B.1

Affiliation:

1. Program of Cellular Biology, Brazilian National Cancer Institute (INCA), Rua André Cavalcanti 37, Centro, 20231-050 Rio de Janeiro, RJ, Brazil

2. Department of Immunobiology, Biology Institute, Fluminense Federal University (UFF), Outeiro São João Batista s/n, Centro, 24020-141 Niterói, RJ, Brazil

Abstract

Interferon- (IFN-)γis an essential cytokine for immunity against intracellular pathogens and cancer. IFN-γexpression by CD4 T lymphocytes is observed only after T helper (Th) 1 differentiation and there are several studies about the molecular mechanisms that control Ifng expression in these cells. However, naïve CD8 T lymphocytes do not produce large amounts of IFN-γ, but after TCR stimulation there is a progressive acquisition of IFN-γexpression during differentiation into cytotoxic T lymphocytes (CTL) and memory cells, which are capable of producing high levels of this cytokine. Differential gene expression can be regulated from the selective action of transcriptional factors and also from epigenetic mechanisms, such as DNA CpG methylation or posttranslational histone modifications. Recently it has been recognized that epigenetic modification is an integral part of CD8 lymphocyte differentiation. This review will focus on the chromatin status of Ifng promoter in CD8 T cells and possible influences of epigenetic modifications in Ifng gene and conserved noncoding sequences (CNSs) in regulation of IFN-γproduction by CD8 T lymphocytes.

Funder

International Centre for Genetic Engineering and Biotechnology

Publisher

Hindawi Limited

Subject

Immunology,General Medicine,Immunology and Allergy

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