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Epigenetic Control of Interferon-Gamma Expression in CD8 T Cells

机译:CD8 T细胞中干扰素-γ表达的表观遗传控制。

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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.
机译:干扰素(IFN-)γ是抵抗细胞内病原体和癌症免疫力的重要细胞因子。 CD4 T淋巴细胞仅在T辅助(Th)1分化后才观察到IFN-γ的表达,并且有一些关于控制这些细胞中Ifng表达的分子机制的研究。但是,幼稚的CD8 T淋巴细胞不会产生大量的IFN-γ,但是在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会逐渐获得IFN-γ的表达,能够产生高水平的这种细胞因子。差异基因的表达可以通过转录因子的选择性作用以及表观遗传机制(例如DNA CpG甲基化或翻译后组蛋白修饰)来调节。最近,已经认识到表观遗传修饰是CD8淋巴细胞分化的组成部分。这项审查将侧重于CD8 T细胞中Ifng启动子的染色质状态,以及Ifng基因和保守非编码序列(CNS)的表观遗传修饰对CD8 T淋巴细胞产生的IFN-γ产生的调节的可能影响。

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