DNA Methylation Profiles of Selected Pro-Inflammatory Cytokines in Alzheimer Disease

Vincenzina Nicolia, R. Cavallaro, Irene López‐González, M. Maccarrone, S. Scarpa, I. Ferrer, A. Fuso
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引用次数: 58

Abstract

By means of functional genomics analysis, we recently described the mRNA expression profiles of various genes involved in the neuroinflammatory response in the brains of subjects with late-onset Alzheimer Disease (LOAD). Some of these genes, namely interleukin (IL)-1&bgr; and IL-6, showed distinct expression profiles with peak expression during the first stages of the disease and control-like levels at later stages. IL-1&bgr; and IL-6 genes are modulated by DNA methylation in different chronic and degenerative diseases; it is also well known that LOAD may have an epigenetic basis. Indeed, we and others have previously reported gene-specific DNA methylation alterations in LOAD and in related animal models. Based on these data, we studied the DNA methylation profiles, at single cytosine resolution, of IL-1&bgr; and IL-6 5’-flanking region by bisulphite modification in the cortex of healthy controls and LOAD patients at 2 different disease stages: Braak I-II/A and Braak V-VI/C. Our analysis provides evidence that neuroinflammation in LOAD is associated with (and possibly mediated by) epigenetic modifications.
阿尔茨海默病中选定的促炎细胞因子的DNA甲基化谱
通过功能基因组学分析,我们最近描述了迟发性阿尔茨海默病(LOAD)受试者大脑中参与神经炎症反应的各种基因的mRNA表达谱。其中一些基因,即白细胞介素(IL)-1;和IL-6,表现出不同的表达谱,在疾病的早期达到峰值,在后期达到控制水平。IL-1&bgr;IL-6基因在不同慢性和退行性疾病中受DNA甲基化调控;众所周知,LOAD可能具有表观遗传基础。事实上,我们和其他人之前已经报道了LOAD和相关动物模型中基因特异性DNA甲基化改变。基于这些数据,我们在单胞嘧啶分辨率下研究了il -1和bgr的DNA甲基化谱;在两个不同疾病阶段(Braak I-II/A和Braak V-VI/C)的健康对照和LOAD患者的皮质中,通过亚硫酸盐修饰IL-6 5 '侧区。我们的分析提供了证据,表明LOAD中的神经炎症与表观遗传修饰有关(并可能由表观遗传修饰介导)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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