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调节性T细胞与表观遗传调控。

Treg Cells and Epigenetic Regulation.

作者信息

Bellanti Joseph A, Li Dongmei

机构信息

Department of Pediatrics, Georgetown University Medical Center, Washington, DC, USA.

Department of Microbiology-Immunology, Georgetown University Medical Center, Washington, DC, USA.

出版信息

Adv Exp Med Biol. 2021;1278:95-114. doi: 10.1007/978-981-15-6407-9_6.

Abstract

The discovery of the epigenetic regulation of Treg cells, a cell population with fundamental immunoregulatory properties, has shed considerable insights into an understanding of the role of these cells in health and disease. Research over the past several years has shown that the interaction of Treg cells with the gut microbiota are critical not only for the development of Treg function in health but also for abnormalities of Treg function that play a critical role in the pathogenesis of human diseases such as the allergic diseases, the autoimmune disorders, and cancer. The equilibrium between phenotypic plasticity and stability of Treg cells is defined by the fine-tuned transcriptional and epigenetic events required to ensure stable expression of Foxp3 in Treg cells. In this chapter, we discuss the molecular events that control Foxp3 gene expression and address the importance of DNA methylation as an important molecular switch that regulates the genetic expression of Treg induction and the possible implications of these findings for the treatment of human diseases characterized by abnormalities of Treg cell function.

摘要

调节性T细胞(Treg细胞)具有基本的免疫调节特性,对其表观遗传调控的发现,为理解这些细胞在健康和疾病中的作用提供了相当多的见解。过去几年的研究表明,Treg细胞与肠道微生物群的相互作用不仅对健康状态下Treg细胞功能的发育至关重要,而且对于Treg细胞功能异常也很关键,而这种异常在诸如过敏性疾病、自身免疫性疾病和癌症等人类疾病的发病机制中起着关键作用。Treg细胞表型可塑性和稳定性之间的平衡,由确保Treg细胞中Foxp3稳定表达所需的精细转录和表观遗传事件所定义。在本章中,我们将讨论控制Foxp3基因表达的分子事件,并阐述DNA甲基化作为调节Treg诱导基因表达的重要分子开关的重要性,以及这些发现对治疗以Treg细胞功能异常为特征的人类疾病可能产生的影响。

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