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MicroRNAs associated with osteoarthritis differently expressed in bone matrix gelatin (BMG) rat model

机译:与骨关节炎相关的MicroRNA在骨基质明胶(BMG)大鼠模型中表达不同

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摘要

Osteoarthritis (OA) is characterized by degeneration of articular cartilage, limited intraarticular inflammation with synovitis, and changes in peri-articular and subchondral bone. In recent years, more and more evidence demonstrated that microRNAs (miRNAs) play important roles in the molecular mechanisms in OA by suppressing gene expression at the post-transcriptional level. In current study, histological staining of toluidine blue and cartilage-specific gene express revealed that the bone matrix gelatin (BMG) rat model could demonstrate the different development of cartilage. In current study, we tested whether some miRNAs associated with OA differently expressed in BMG rat model. We verified that miR-140 and miR-455 were associated with cartilage development, and further revealed that miR-140-5p and miR-455-3p might play more important function than miR-140-3p and miR-455-5p in the BMG rat model. Moreover, we found that miR-9 and miR-98 were involved in the endochondral ossification, suggesting they may be also the key regulators in the process of endochondral ossification. In fact, many miRNAs worked as a miRNA-mediated regulatory network in the process of cartilage development and OA. Further functional discovery will clarify the roles of individual miRNAs and their targets, and serve as a strong foundation for translating these findings to the clinic therapy for OA.
机译:骨关节炎(OA)的特征是关节软骨退变,关节内炎症伴滑膜炎受限以及关节周围和软骨下骨的变化。近年来,越来越多的证据表明,microRNA(miRNA)通过在转录后水平上抑制基因表达在OA的分子机制中发挥重要作用。在当前的研究中,甲苯胺蓝和软骨特异性基因表达的组织学染色显示,骨基质明胶(BMG)大鼠模型可以证明软骨的不同发展。在当前的研究中,我们测试了一些与OA相关的miRNA在BMG大鼠模型中是否表达不同。我们验证了miR-140和miR-455与软骨发育有关,并进一步揭示了miR-140-5p和miR-455-3p可能比miR-140-3p和miR-455-5p更重要。 BMG大鼠模型。此外,我们发现miR-9和miR-98参与了软骨内骨化,这表明它们可能也是软骨内骨化过程中的关键调控因子。实际上,许多miRNA在软骨发育和OA的过程中起着miRNA介导的调控网络的作用。进一步的功能发现将阐明单个miRNA及其靶标的作用,并为将这些发现转化为OA的临床疗法奠定坚实的基础。

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