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B细胞疾病的表观遗传学观点。

An epigenetic view of B-cell disorders.

作者信息

Alberghini Federica, Petrocelli Valentina, Rahmat Mahshid, Casola Stefano

机构信息

IFOM, The FIRC Institute of Molecular Oncology Foundation, Milan, Italy.

出版信息

Immunol Cell Biol. 2015 Mar;93(3):253-60. doi: 10.1038/icb.2014.116. Epub 2015 Jan 20.

Abstract

B-cell development is a multistep process sustained by a highly coordinated transcriptional network under the control of a limited set of transcription factors. Epigenetic mechanisms, including DNA methylation, histone posttranslational modifications and microRNAs act in concert with transcription factors to promote lineage commitment, define and sustain cell identity and establish heritable cell-type- and stage-specific gene expression profiles. Epigenetic modifiers have recently emerged as key regulators of B-cell development and activation. Central to B-cell-mediated immunity are germinal centers, transient structures formed in secondary lymphoid organs where antigen-specific B cells undergo intense proliferation, immunoglobulin somatic hypermutation and isotype switching, to generate ultimately long-lived memory B cells and terminally differentiated plasma cells expressing high-affinity antibodies. Deregulation of one or more epigenetic axes represents a common feature of several B-cell disorders arising from germinal center B cells, including autoimmunity and lymphoma. Moreover, the hijacking of epigenetic determinants is central to the ability of the B-lymphotropic Epstein-Barr virus (EBV) to establish, via the germinal center reaction, life-long latency and occasionally contribute to malignant B-cell transformation. In the light of recent findings, this review will discuss the relevance of epigenetic deregulation in the pathogenesis of B-cell diseases. Understanding how specific epigenetic alterations contribute to the development of lymphomas, autoimmunity and EBV-associated disorders is instrumental to develop novel therapeutic interventions for the cure of these often fatal pathologies.

摘要

B细胞发育是一个多步骤过程,由一组有限的转录因子控制下的高度协调的转录网络维持。表观遗传机制,包括DNA甲基化、组蛋白翻译后修饰和微小RNA,与转录因子协同作用,促进谱系定向、定义和维持细胞身份,并建立可遗传的细胞类型和阶段特异性基因表达谱。表观遗传修饰因子最近已成为B细胞发育和激活的关键调节因子。生发中心是B细胞介导免疫的核心,生发中心是在次级淋巴器官中形成的短暂结构,抗原特异性B细胞在其中经历强烈增殖、免疫球蛋白体细胞超突变和同种型转换,最终产生长寿记忆B细胞和表达高亲和力抗体的终末分化浆细胞。一个或多个表观遗传轴的失调是由生发中心B细胞引起的几种B细胞疾病的共同特征,包括自身免疫和淋巴瘤。此外,表观遗传决定因素的劫持对于嗜B淋巴细胞的EB病毒(EBV)通过生发中心反应建立终身潜伏并偶尔促成恶性B细胞转化的能力至关重要。鉴于最近的发现,本综述将讨论表观遗传失调在B细胞疾病发病机制中的相关性。了解特定的表观遗传改变如何导致淋巴瘤、自身免疫和EBV相关疾病的发展,有助于开发治疗这些通常致命疾病的新型治疗干预措施。

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