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CD8 T 细胞中干扰素-γ表达的表观遗传控制。

Epigenetic control of interferon-gamma expression in CD8 T cells.

机构信息

Program of Cellular Biology, Brazilian National Cancer Institute (INCA), Rua André Cavalcanti 37, Centro, 20231-050 Rio de Janeiro, RJ, Brazil ; Department of Immunobiology, Biology Institute, Fluminense Federal University (UFF), Outeiro São João Batista s/n, Centro, 24020-141 Niterói, RJ, Brazil.

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

出版信息

J Immunol Res. 2015;2015:849573. doi: 10.1155/2015/849573. Epub 2015 Apr 20.


DOI:10.1155/2015/849573
PMID:25973438
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4418004/
Abstract

Interferon- (IFN-) γ is an essential cytokine for immunity against intracellular pathogens and cancer. IFN-γ 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, naïve CD8 T lymphocytes do not produce large amounts of IFN-γ, but after TCR stimulation there is a progressive acquisition of IFN-γ 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-γ production by CD8 T lymphocytes.

摘要

干扰素- (IFN-) γ 是一种对抗细胞内病原体和癌症的重要细胞因子。CD4 T 淋巴细胞中的 IFN-γ 表达仅在 T 辅助 (Th) 1 分化后观察到,有许多研究涉及控制这些细胞中 Ifng 表达的分子机制。然而,幼稚 CD8 T 淋巴细胞不会产生大量 IFN-γ,但在 TCR 刺激后,在分化为细胞毒性 T 淋巴细胞 (CTL) 和记忆细胞的过程中,IFN-γ 的表达逐渐获得,这些细胞能够产生高水平的这种细胞因子。差异基因表达可以通过转录因子的选择性作用以及表观遗传机制来调节,例如 DNA CpG 甲基化或翻译后组蛋白修饰。最近,人们已经认识到表观遗传修饰是 CD8 淋巴细胞分化的一个组成部分。这篇综述将重点介绍 CD8 T 细胞中 Ifng 启动子的染色质状态,以及表观遗传修饰对 IFN-γ 产生的 CD8 T 淋巴细胞中 Ifng 基因和保守非编码序列 (CNSs) 的调控可能产生的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59d7/4418004/7dcdf1ae5cbf/JIR2015-849573.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59d7/4418004/7dcdf1ae5cbf/JIR2015-849573.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59d7/4418004/7dcdf1ae5cbf/JIR2015-849573.001.jpg

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本文引用的文献

[1]
Transcription factor T-bet regulates intraepithelial lymphocyte functional maturation.

Immunity. 2014-8-21

[2]
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Nat Rev Immunol. 2014-9

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