Epigenetic Control of Interferon-Gamma Expression in CD8 T Cells

被引:59
|
作者
de Araujo-Souza, Patricia S. [1 ,2 ]
Hanschke, Steffi C. H. [1 ]
Viola, Joao P. B. [1 ]
机构
[1] Brazilian Natl Canc Inst INCA, Program Cellular Biol, BR-20231050 Rio De Janeiro, RJ, Brazil
[2] Univ Fed Fluminense, Inst Biol, Dept Immunobiol, BR-24020141 Niteroi, RJ, Brazil
关键词
DISTAL REGULATORY ELEMENTS; IFN-GAMMA; TRANSCRIPTION FACTOR; DNA METHYLATION; CUTTING EDGE; EFFECTOR; MEMORY; DIFFERENTIATION; NAIVE; LYMPHOCYTES;
D O I
10.1155/2015/849573
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Interferon-(IFN-) gamma is an essential cytokine for immunity against intracellular pathogens and cancer. IFN-gamma expression 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, naive CD8 T lymphocytes do not produce large amounts of IFN-gamma, but after TCR stimulation there is a progressive acquisition of IFN-gamma expression 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-gamma production by CD8 T lymphocytes.
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页数:7
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