Nicolia Vincenzina, Cavallaro Rosaria A, López-González Irene, Maccarrone Mauro, Scarpa Sigfrido, Ferrer Isidre, Fuso Andrea
Department of Surgery "P. Valdoni", Sapienza University of Rome, Italy.
Neuropathology, Service of Pathology, Bellvitge University Hospital; and University of Barcelona, Hospitalet de LLobregat, Spain.
J Neuropathol Exp Neurol. 2017 Jan 1;76(1):27-31. doi: 10.1093/jnen/nlw099.
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)-1β 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-1β 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-1β 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.
通过功能基因组学分析,我们最近描述了晚发性阿尔茨海默病(LOAD)患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)-1β和IL-6,表现出独特的表达谱,在疾病的第一阶段表达达到峰值,在后期阶段则接近对照水平。在不同的慢性和退行性疾病中,IL-1β和IL-6基因受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及相关动物模型中基因特异性的DNA甲基化改变。基于这些数据,我们通过亚硫酸氢盐修饰,在单胞嘧啶分辨率下研究了健康对照和处于两个不同疾病阶段(Braak I-II/A和Braak V-VI/C)的LOAD患者大脑皮质中IL-1β和IL-6 5'侧翼区域的DNA甲基化谱。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相关(并且可能由表观遗传修饰介导)。