Suppr超能文献

沉默长链非编码 RNA NEAT1 通过下调 microRNA-129 和 microRNA-204 抑制 MAPK/ERK 信号通路来减轻类风湿关节炎。

Silencing long non-coding RNA NEAT1 attenuates rheumatoid arthritis via the MAPK/ERK signalling pathway by downregulating microRNA-129 and microRNA-204.

机构信息

Department of Rheumatology and Immunology, The Affiliated Hospital of Southwest Medical University, Luzhou, P.R. China.

Department of Ophthalmology, The Affiliated Hospital of Southwest Medical University, Luzhou, P.R. China.

出版信息

RNA Biol. 2021 May;18(5):657-668. doi: 10.1080/15476286.2020.1857941. Epub 2021 Jan 20.

Abstract

The participation of long noncoding RNAs (lncRNAs) and microRNAs (miRs) in the progression of rheumatoid arthritis (RA) is a key area of investigation. The current study aimed to investigate the action of lncRNA nuclear paraspeckle assembly transcript 1 (NEAT1) in fibroblast-like synoviocyte (FLS) proliferation and synovitis in RA. A rat model of RA was established. LncRNA NEAT1 expression in the synovial tissues of patients with RA and FLSs from the RA rat model was determined using RT-qPCR. Next, dual luciferase reporter gene assay was applied to investigate the relationship between miR-129/204 and mitogen-activated protein kinase (MAPK)/extracellular regulated protein kinase (ERK). A putative binding relationship between miR-204 and lncRNA NEAT1 was evaluated by RIP assay, and miR-129 promoter methylation was determined using MSP. After the expression of lncRNA NEAT1, miR-129 or miR-204 was altered in FLSs, the extent of ERK1/2 phosphorylation was assessed. In addition, FLS synovitis and proliferation were determined by ELISA and EdU assay, respectively. In RA rats, lncRNA NEAT1 was silenced and miR-129/miR-204 was overexpressed to explore their roles . LncRNA NEAT1 was upregulated, while miR-129 and miR-204 were downregulated in RA synovial tissues and FLSs. MAPK1 was target gene of both miR-129 and miR-204. LncRNA NEAT1 bound to miR-204 and promoted miR-129 promoter methylation. Silencing lncRNA NEAT1 or overexpressing miR-129/miR-204 enhanced miR-129/miR-204 expression, but reduced the extent of ERK1/2 phosphorylation, proliferation of FLSs, and synovitis in RA. Collectively, silencing lncRNA NEAT1 promoted miR-129 and miR-204 to inhibit the MAPK/ERK signalling pathway, reducing FLS synovitis in RA. ACR: American College of Rheumatology; ELISA: Enzyme-linked immunosorbent assay; ERK: extracellular signal-regulated kinase; FLS: fibroblast-like synoviocyte; GADPH: glyceraldehyde-3-phosphate dehydrogenase; HRP: horseradish peroxidase; IFA: Incomplete Freund's Adjuvant; lncRNAs: long noncoding RNAs; MSP: Methylation-specific PCR; NC: negative control; NEAT1: nuclear paraspeckle assembly transcript 1; OD: optical density; RA: rheumatoid arthritis; RIPA: Radio Immunoprecipitation Assay; RLU: relative light units; RT-qPCR: reverse transcription quantitative polymerase chain reaction; UTR: untranslated region.

摘要

长链非编码 RNA(lncRNAs)和 microRNAs(miRs)在类风湿关节炎(RA)进展中的参与是一个关键的研究领域。本研究旨在探讨核斑蛋白组装转录物 1(NEAT1)lncRNA 在 RA 成纤维样滑膜细胞(FLS)增殖和滑膜炎中的作用。建立了 RA 大鼠模型。采用 RT-qPCR 检测 RA 患者滑膜组织和 RA 大鼠模型中 FLS 中 lncRNA NEAT1 的表达。接下来,应用双荧光素酶报告基因检测 miR-129/204 与丝裂原活化蛋白激酶(MAPK)/细胞外调节蛋白激酶(ERK)之间的关系。通过 RIP 测定评估 miR-204 与 lncRNA NEAT1 之间的假定结合关系,并通过 MSP 测定评估 miR-129 启动子甲基化。改变 FLS 中 lncRNA NEAT1、miR-129 或 miR-204 的表达后,评估 ERK1/2 磷酸化程度。此外,通过 ELISA 和 EdU 测定分别检测 FLS 滑膜炎和增殖。在 RA 大鼠中,沉默 lncRNA NEAT1 并过表达 miR-129/miR-204 以探讨其作用。结果显示,在 RA 滑膜组织和 FLS 中,lncRNA NEAT1 上调,而 miR-129 和 miR-204 下调。MAPK1 是 miR-129 和 miR-204 的共同靶基因。lncRNA NEAT1 与 miR-204 结合,并促进 miR-129 启动子甲基化。沉默 lncRNA NEAT1 或过表达 miR-129/miR-204 增强了 miR-129/miR-204 的表达,但降低了 ERK1/2 磷酸化、FLS 增殖和 RA 滑膜炎的程度。综上所述,沉默 lncRNA NEAT1 可促进 miR-129 和 miR-204 抑制 MAPK/ERK 信号通路,减少 RA 中 FLS 的滑膜炎。ACR:美国风湿病学会;ELISA:酶联免疫吸附测定;ERK:细胞外信号调节激酶;FLS:成纤维样滑膜细胞;GAPDH:甘油醛-3-磷酸脱氢酶;HRP:辣根过氧化物酶;IFA:不完全弗氏佐剂;lncRNAs:长链非编码 RNA;MSP:甲基化特异性 PCR;NC:阴性对照;NEAT1:核斑蛋白组装转录物 1;OD:光密度;RA:类风湿关节炎;RIPA:放射性免疫沉淀测定;RLU:相对光单位;RT-qPCR:逆转录定量聚合酶链反应;UTR:非翻译区。

相似文献

引用本文的文献

5
Resolution of inflammation during rheumatoid arthritis.类风湿关节炎炎症的消退
Front Cell Dev Biol. 2025 Mar 26;13:1556359. doi: 10.3389/fcell.2025.1556359. eCollection 2025.

本文引用的文献

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验