| Literature DB >> 28053004 |
Vincenzina Nicolia1, Rosaria A Cavallaro1, Irene López-González2, Mauro Maccarrone3,4, Sigfrido Scarpa1, Isidre Ferrer1,2, Andrea Fuso3.
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)-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.Entities:
Keywords: Alzheimer disease; Cytokines; DNA methylation; Epigenetics; Neuroinflammation; Non-CpG methylation
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Year: 2017 PMID: 28053004 DOI: 10.1093/jnen/nlw099
Source DB: PubMed Journal: J Neuropathol Exp Neurol ISSN: 0022-3069 Impact factor: 3.685