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表观遗传学修饰:系统性硬化症的新型治疗策略?

Epigenetic modifications: novel therapeutic strategies for systemic sclerosis?

机构信息

Center of Experimental Rheumatology, University Hospital Zurich, Zurich Center of Integrative Human Physiology, Switzerland.

出版信息

Expert Rev Clin Immunol. 2011 Jul;7(4):475-80. doi: 10.1586/eci.11.37.

Abstract

Epigenetic modifications of gene expression comprise modifications of DNA by DNA methylation and modifications of the histone proteins by acetylation, methylation, SUMOylation or phosphorylation. DNA methylation in the promoter region of genes represses gene transcription. Histone modifications influence the structure of DNA and regulate gene expression by changing the availability of DNA for the transcriptional machinery or DNA-binding proteins. Histone modifications are mediated by enzymes and induce or repress gene expression. Aberrant expression of single enzymes disturb the normal balance of these modifiers leading to cancer or autoimmune diseases. We show in this article that epigenetic modifications contribute to the massive production of extracellular matrix proteins in systemic sclerosis skin fibroblasts. Both DNA methylation and histone modifications contribute to the activated phenotype of systemic sclerosis fibroblasts. In vitro and in vivo experiments demonstrate that the use of epigenetic-based drugs on these cells is able to reverse their activated phenotype.

摘要

基因表达的表观遗传修饰包括 DNA 的 DNA 甲基化修饰和组蛋白的乙酰化、甲基化、SUMO 化或磷酸化修饰。基因启动子区域的 DNA 甲基化抑制基因转录。组蛋白修饰通过改变转录机器或 DNA 结合蛋白对 DNA 的可及性来影响 DNA 结构并调节基因表达。组蛋白修饰由酶介导,并诱导或抑制基因表达。单个酶的异常表达会破坏这些修饰物的正常平衡,导致癌症或自身免疫性疾病。我们在本文中表明,表观遗传修饰有助于系统性硬化症皮肤成纤维细胞中细胞外基质蛋白的大量产生。DNA 甲基化和组蛋白修饰均有助于系统性硬化症成纤维细胞的激活表型。体外和体内实验表明,在这些细胞上使用基于表观遗传的药物能够逆转其激活表型。

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