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首页> 外文期刊>RNA biology >Gastrodin promotes CNS myelination via a lncRNA Gm7237/miR-142a/MRF pathway
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Gastrodin promotes CNS myelination via a lncRNA Gm7237/miR-142a/MRF pathway

机译:天麻素通过 lncRNA Gm7237/miR-142a/MRF 通路促进中枢神经系统髓鞘形成

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Treatment of central nervous system (CNS) demyelination is greatly hindered by lack of the knowledge regarding to underlying molecular mechanisms as well as therapeutic agents. Here, we report a novel small molecule agent, gastrodin (GAS), which can significantly promote CNS myelination in in vivo mice models. By using high-throughput sequencing analysis, we discover a key long non-coding RNA Gm7237 that can enhance CNS myelination and is up-regulated by GAS. Through using bioinformatic analysis and experimental validations, we further unravel that microRNA-142a (miR-142a) and its target myelin gene regulatory factor (MRF) is under the direct regulation by Gm7237. Finally, we demonstrate that Gm7237/miR-142a/MRF axis is the key pathway involved in CNS myelination mediated by GAS. Overall, our results provide not only a novel agent for therapeutic treatment of CNS demyelination but also a molecular basis responsible for GAS-promoted CNS myelination.
机译:由于缺乏对潜在分子机制和治疗剂的了解,中枢神经系统 (CNS) 脱髓鞘的治疗受到极大阻碍。在这里,我们报道了一种新型小分子药物天麻素(GAS),它可以在体内小鼠模型中显着促进中枢神经系统髓鞘形成。通过使用高通量测序分析,我们发现了一种关键的长链非编码RNA Gm7237,它可以增强CNS髓鞘形成,并被GAS上调。通过生物信息学分析和实验验证,我们进一步揭示了microRNA-142a(miR-142a)及其靶髓鞘基因调控因子(MRF)受Gm7237的直接调控。最后,我们证明了 Gm7237/miR-142a/MRF 轴是 GAS 介导的 CNS 髓鞘形成的关键途径。总体而言,我们的研究结果不仅为中枢神经系统脱髓鞘的治疗提供了一种新药,而且还为GAS促进的中枢神经系统髓鞘形成提供了分子基础。

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