DNA methylation profiling in different phases of temporomandibular joint osteoarthritis in rats. (August 2016)

• Record Type: Journal Article
• Authors: Xiao, Jia-Ling; Meng, Juan-Hong; Gan, Ye-Hua; Li, Ya-Li; Zhou, Chun-Yan; Ma, Xu-Chen
• Is Part Of: Archives of oral biology. Volume 68(2016)
• Page Start: 105
• Page End: 115
• Publication Date: 2016-08
• Subjects: Temporomandibular joint -- Osteoarthritis -- DNA methylation -- Claudin11; Mouth -- Periodicals; Mouth -- Diseases -- Periodicals; Dentistry -- Periodicals; Electronic journals; 617.6005
• DOI: 10.1016/j.archoralbio.2016.04.006
• Languages: English
• ISSNs: 0003-9969

Abstract

Highlights: DNA methylation was evaluated in the mandibular head cartilage in the early, intermediate and late phases of rat TMJOA;. Different DNA methylation changes have been detected during the different stages of TMJOA;. A host of novel differentially methylated pathways and genes, including the CLDN11 and CHAD, were observed in the progression of TMJOA. Abstract: Objective: Temporomandibular joint osteoarthritis (TMJOA) is a complex disease with strong genetic and epigenetic components in its pathogenesis. The aim of this study was to evaluate DNA methylation in mandibular head cartilage in different phases of experimentally-induced TMJOA in rats. Design: DNA methylation was evaluated using microarrays in the mandibular head cartilage of early, intermediate and late stage experimentally-induced TMJOA, and of the normal age-matched control groups. Genes with differentially methylated CpG sites were analyzed to reveal the over-represented gene ontologies and pathways at different stages, and were compared with published expression profiles to assess their overlappings. The DNA methylation patterns of the target genes were validated by methylated DNA immunoprecipitation qPCR in additional independent cartilage samples and mRNA levels were analyzed by real-time PCR. Results: We observed 9489 differentially methylated regions between the TMJOA and controls. A total of 440 consistently altered genes were revealed in all three stages; most (80%) were hypomethylated and many were associated with cell cycle regulation. We also detected different DNA methylation changes in early and late stage TMJOA (Rearly = 0.68, Rlate = 0.47), while the differences between age-matched healthy cartilage were subtle. Strong inverse changes between methylation status and mRNA levels were confirmed in Adamts5, Chad, Cldn11 and Tnf . Conclusions: Our data reveals dynamic DNA methylation patterns during the progression of TMJOA, with a different host of genes and pathways. The changes of cartilage DNA methylation patterns might contribute to understand the etiologic mechanisms of TMJOA epigenetically.