Division of Gastroenterology, Infectiology and Rheumatology, Medical Department, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Department of Biology, Chemistry and Pharmacy, Freie Universität Berlin, Berlin, Germany.
Front Immunol. 2019 Nov 26;10:2718. doi: 10.3389/fimmu.2019.02718. eCollection 2019.
Epigenetic programs that control posttranslational modifications of histone proteins and DNA itself tightly regulate transcriptional networks determining the identity and function of CD8 T cells. Chromatin-modifying enzymes such as histone acetyltransferases and deacetylases, represent key molecular determinants of the epigenetic imprinting of CD8 T cells. The functions of these enzymes highly depend on the availability of key products of cellular metabolism pathways such as acetyl-CoA, NAD (Nicotinamide adenine dinucleotide) and SEM (S-adenosylmethionine), suggesting that there is a close crosstalk between the metabolic and the epigenetic regulation of CD8 T cells. In this review, we will discuss the metabolic regulation of CD8 T cell epigenetics during activation and differentiation. We will furthermore summarize how metabolic signals from the tumor microenvironment (TME) shape the epigenetic landscape of CD8 T cells to better understand the mechanism underlying CD8 T cell exhaustion in anti-tumor and anti-viral immunity, which might help to overcome limitations of current CD8 T cell-based therapies.
表观遗传程序控制组蛋白蛋白和 DNA 本身的翻译后修饰,紧密调节决定 CD8 T 细胞身份和功能的转录网络。染色质修饰酶,如组蛋白乙酰转移酶和去乙酰化酶,是 CD8 T 细胞表观遗传印记的关键分子决定因素。这些酶的功能高度依赖于细胞代谢途径的关键产物的可用性,如乙酰辅酶 A、NAD(烟酰胺腺嘌呤二核苷酸)和 SEM(S-腺苷甲硫氨酸),这表明代谢和 CD8 T 细胞的表观遗传调控之间存在密切的相互作用。在这篇综述中,我们将讨论 CD8 T 细胞激活和分化过程中细胞表观遗传的代谢调控。我们还将总结肿瘤微环境(TME)中的代谢信号如何塑造 CD8 T 细胞的表观遗传景观,以更好地理解抗肿瘤和抗病毒免疫中 CD8 T 细胞耗竭的机制,这可能有助于克服当前基于 CD8 T 细胞疗法的局限性。