Electroacupuncture stimulating Neixiyan (EX-LE5) and Dubi (ST35) alleviates osteoarthritis in rats induced by anterior cruciate ligament transaction affecting DNA methylation regulated transcription of miR-146a and miR-140-5p.

Ding Luobin, Wang Huajun, L I Yao, L I Jia, L I Ling, Gao Yangping, Guan Jian, Geng Weiqiang
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Abstract

Objective: To explore whether electroacupuncture (EA) could alleviate osteoarthritis (OA) through affecting the DNA methylation regulated transcription of miR-146a and miR-140-5p.

Methods: Sixty male eight-week-old Sprague-Dawley rats were divided into three groups: normal group (normal healthy rats; no treatment), model group (OA rats; no treatment) and EA group (OA rats treated with EA). Safranin O staining and modified Mankin's score were performed to evaluate the histopathological alterations and degeneration of cartilage 8 weeks after 8 consecutive weeks of treatment. Quantitative real time polymerase chain reaction (qRT-PCR) assay was employed to evaluate the expression of miR-146a in the cartilage tissue and miR-140-5p in the synovium tissue, respectively. The bisulfite sequencing analysis and quantitative methylation specific PCR (qMSP) were used to analyze the status of methylation in the regulatory regions of miR-146a and miR-140-5p. Chromatin immunoprecipitation (ChIP) assay were performed to assess the binding of nuclear factor-kappa B (NF-κB) and signal transducer and activator of transcription 3 (SMAD-3) in the regulatory regions of miR-146a and miR-140-5p. Western blot analysis was performed to detect the expressions of DNA Methyltransferase 1 (DMNT1), DNA Methyltransferase 3A (DMNT3A), and DNA Methyltransferase 3A (DMNT3b), NF-κB, SMAD3 levels.

Results: Our results showed that EA treatment significantly upregulated miR-146a and miR-140-5p expressions. qMSP analysis showed that EA significantly decreased methylation levels of miR-140-5p regulated region and miR-146a promoter in OA cartilage and synovium. Bisulfite DNA sequencing (BDS) and ChIP analysis showed that EA significantly increased binding affinity of SMAD3 and NF-kB on the hypermethylated miR-140 regulatory region and miR-146a promoter, respectively. Western Blot analysis demonstrated that EA also significantly decreased expressions of methylation related proteins- DMNT1, DMNT3a, and DMNT3b as well as NF-κB and SMAD3.

Conclusions: Electroacupuncture stimulating Neixiyan (EX-LE5) and Dubi (ST35) may alleviate OA affecting the DNA methylation regulated transcription of miR-146a and miR-140-5p.

电针刺激内西炎(EX-LE5)和杜比(ST35)减轻前交叉韧带交易诱导的大鼠骨关节炎,影响miR-146a和miR-140-5p的DNA甲基化调节转录。
目的:探讨电针(EA)是否通过影响miR-146a和miR-140-5p的DNA甲基化调控转录来减轻骨关节炎(OA)。进行番红O染色和改良曼金评分,以评估连续8周治疗后8周软骨的组织病理学改变和变性。采用定量实时聚合酶链式反应(qRT-PCR)测定分别评估miR-146a在软骨组织中和miR-140-5p在滑膜组织中的表达。亚硫酸氢盐测序分析和定量甲基化特异性PCR(qMSP)用于分析miR-146a和miR-140-5p调控区的甲基化状态。进行染色质免疫沉淀(ChIP)测定以评估核因子κB(NF-κB)和信号转导子和转录激活子3(SMAD-3)在miR-146a和miR-140-5p的调节区中的结合。Western印迹分析检测DNA甲基转移酶1(DMNT1)、DNA甲基转移蛋白酶3A(DMNT3A)和DNA甲基转移酶类3A(DMNT3b)的表达、NF-κB和SMAD3水平。结果:我们的研究结果表明,电针治疗显著上调了miR-146a和miR-140-5p的表达。qMSP分析显示,EA显著降低OA软骨和滑膜中miR-140-5p调节区和miR-146a启动子的甲基化水平。双硫化物DNA测序(BDS)和ChIP分析显示,EA分别显著增加了SMAD3和NF-kB对超甲基化miR-140调控区和miR-146a启动子的结合亲和力。Western Blot分析表明,电针还显著降低了甲基化相关蛋白DMNT1、DMNT3a和DMNT3b以及NF-κB和SMAD3的表达。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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