Cell-specific epigenome-wide DNA methylation profile in long-term cultured minor salivary gland epithelial cells from patients with Sjögren's syndrome

DNA甲基化 表观基因组 表观遗传学 甲基化 基因 发病机制 医学 自身抗体 CpG站点 免疫学 唾液腺 生物 计算生物学 遗传学 分子生物学 内科学 基因表达 抗体
作者
Amandine Charras,Orsia D Konsta,Christelle Le Dantec,Cristina Bagacean,Efstathia K. Kapsogeorgou,Athanasios G. Tzioufas,Jacques‐Olivier Pers,Anne Bordron,Yves Renaudineau
出处
期刊:Annals of the Rheumatic Diseases [BMJ]
卷期号:76 (3): 625-628 被引量:47
标识
DOI:10.1136/annrheumdis-2016-210167
摘要

The aetiology of primary Sjögren's syndrome (pSS), also referred to as autoimmune epithelitis, is incompletely understood but includes an epigenetic contribution. Accordingly, the aim of this study was to investigate DNA methylation in salivary gland epithelial cells (SGEC), and to compare results with those publicly available from pSS B and T cells.Long-term cultured SGEC were selected to conduct an epigenome-wide association study (EWAS) in patients with pSS with comparison to controls using the HumanMethylation 450 K array from Illumina.The analysis of differentially methylated CpG (DMC) uncovered 4662 positions corresponding to 2560 genes, and 575 genes with two or more DMC sites (DMCs), in SGEC as compared with controls. Further analysis highlighted an important proportion of interferon-regulated genes (61%), the calcium pathway (hypomethylated) and the Wnt pathway (hypermethylated). When comparing SGEC with pSS T and/or B cell results, an important overlap was observed with respect to differentially methylated genes (38.8%) and pSS risk factors (71.4%), although such assertion was not true when comparing DMCs.This study conducted in SGEC emphasises the role of DNA methylation in pSS pathogenesis and supports the necessity to conduct pure cell analysis for future EWAS studies when analysing salivary glands from patients with pSS.
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