| Literature DB >> 33151124 |
Yue Shu1,2, Tianyuan Luo2,3, Mingda Wang1,4, Yu Zhang2,3, Lin Zhang2,3, Zhi Xiao1, Qianxing Wang4, Qiang Zhang1,5, Jia Zou1, Changyin Yu1,6, Shangfu Xu7, Tian Yu1,2, Liang Zhou1, Shouyang Yu1,2.
Abstract
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.Entities:
Keywords: Gastrodin; lncRNA; microRNA; myelination
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Year: 2020 PMID: 33151124 PMCID: PMC8354603 DOI: 10.1080/15476286.2020.1841976
Source DB: PubMed Journal: RNA Biol ISSN: 1547-6286 Impact factor: 4.652