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微小RNA-26a-5p通过激活人骨关节炎软骨细胞中的核因子κB途径调控诱导型一氧化氮合酶的表达。

MicroRNA-26a-5p regulates the expression of inducible nitric oxide synthase via activation of NF-κB pathway in human osteoarthritis chondrocytes.

作者信息

Rasheed Zafar, Al-Shobaili Hani A, Rasheed Naila, Mahmood Amer, Khan Mohammed Imran

机构信息

Department of Medical Biochemistry, College of Medicine, Qassim University, Buraidah, Saudi Arabia.

Department of Dermatology, College of Medicine, Qassim University, Saudi Arabia.

出版信息

Arch Biochem Biophys. 2016 Mar 15;594:61-7. doi: 10.1016/j.abb.2016.02.003. Epub 2016 Feb 27.

Abstract

Inducible nitric oxide synthase (iNOS) expression is associated with the pathogenesis of osteoarthritis (OA). This study was undertaken to investigate whether interleukin-1β (IL-1β)-mediated induction of iNOS can be regulated by microRNA-26a-5p (hsa-miR-26a-5p) in OA. Bioinformatics approaches show that 3'UTR of iNOS mRNA contained the 'seed-matched-sequence' for hsa-miR-26a-5p. IL-1β-induced expression of iNOS correlated with the down-regulation of miR-26a-5p in human OA chondrocytes. hsa-miR-26a-5p directly suppressed the luciferase activity of 3'UTR-iNOS reporter clone. Transfection with pre-miR-26a-5p induced marked silencing of iNOS expression. Activation of NF-κB pathway down-regulated the expression of hsa-miR-26a-5p and induced iNOS expression. In short, this is the first report that shows hsa-miR-26a-5p is a direct regulator of iNOS expression in human chondrocytes. hsa-miR-26a-5p may be an important regulator of human cartilage homeostasis and a new target for OA therapy.

摘要

诱导型一氧化氮合酶(iNOS)的表达与骨关节炎(OA)的发病机制相关。本研究旨在探讨在OA中,白细胞介素-1β(IL-1β)介导的iNOS诱导是否受微小RNA-26a-5p(hsa-miR-26a-5p)调控。生物信息学方法显示,iNOS mRNA的3'非翻译区(3'UTR)含有与hsa-miR-26a-5p的“种子匹配序列”。在人OA软骨细胞中,IL-1β诱导的iNOS表达与miR-26a-5p的下调相关。hsa-miR-26a-5p直接抑制3'UTR-iNOS报告基因克隆的荧光素酶活性。转染pre-miR-26a-5p可显著沉默iNOS表达。NF-κB信号通路的激活下调了hsa-miR-26a-5p的表达并诱导了iNOS表达。简而言之,这是首次报道hsa-miR-26a-5p是人类软骨细胞中iNOS表达的直接调节因子。hsa-miR-26a-5p可能是人类软骨稳态的重要调节因子及OA治疗的新靶点。

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