阿尔茨海默病中选定的促炎细胞因子的DNA甲基化谱

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

摘要

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