Irisin-regulated lncRNAs and their potential regulatory functions in chondrogenic differentiation of human mesenchymal stem cells.

IF 1.7 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL Open Medicine Pub Date : 2024-11-15 eCollection Date: 2024-01-01 DOI:10.1515/med-2024-1073
Yijie Chen, Wenqi Sha, Yifan Zhang, Wanyi Kou, Liu Yang, Ruixin Guo, Chenyang Li, Junjie Zhao, Zhenghui Wang
{"title":"Irisin-regulated lncRNAs and their potential regulatory functions in chondrogenic differentiation of human mesenchymal stem cells.","authors":"Yijie Chen, Wenqi Sha, Yifan Zhang, Wanyi Kou, Liu Yang, Ruixin Guo, Chenyang Li, Junjie Zhao, Zhenghui Wang","doi":"10.1515/med-2024-1073","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>Dysregulation of chondrogenic differentiation is associated with osteoarthritis (OA). The myokine irisin is beneficial in OA treatment; yet, the underlying mechanism is not fully understood. Long noncoding RNAs (lncRNAs) act as important regulators of chondrocyte differentiation. This study was conducted to address the role of lncRNAs in mediating irisin-induced chondrocyte differentiation.</p><p><strong>Methods: </strong>We investigated the irisin-regulated lncRNA profile change in human mesenchymal stem cells (MSCs) using published whole transcriptome sequencing data. We predicted their potential targets and competitive endogenous RNA (ceRNA) prediction and analyzed their molecular functions using functional enrichment analysis.</p><p><strong>Results: </strong>More differentially expressed lncRNAs (DElncRNAs) were observed in irisin-treated samples. The top irisin-induced lncRNAs were associated with OA or chondrogenic differentiation, including <i>XIST</i>, <i>PAX8-AS1</i>, <i>CASC15</i>, <i>LINC01618</i>, and <i>DLX6-AS1</i>. The DEGs co-expressed with DElncRNAs were enriched in skeletal system development, extracellular matrix (ECM) organization, cell adhesion, and inflammation associated pathways. Several lncRNAs likely acted as ceRNAs to regulate downstream mRNAs including <i>ROR2</i> and <i>SORBS1</i> in in OA or chondrogenic differentiation.</p><p><strong>Conclusions: </strong>We demonstrate the global regulation of lncRNAs by irisin during chondrogenic differentiation of human MSCs. Further study is required to characterize the key irisin-regulated lncRNAs in chondrogenic differentiation.</p>","PeriodicalId":19715,"journal":{"name":"Open Medicine","volume":"19 1","pages":"20241073"},"PeriodicalIF":1.7000,"publicationDate":"2024-11-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11587921/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Open Medicine","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1515/med-2024-1073","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
引用次数: 0

Abstract

Objective: Dysregulation of chondrogenic differentiation is associated with osteoarthritis (OA). The myokine irisin is beneficial in OA treatment; yet, the underlying mechanism is not fully understood. Long noncoding RNAs (lncRNAs) act as important regulators of chondrocyte differentiation. This study was conducted to address the role of lncRNAs in mediating irisin-induced chondrocyte differentiation.

Methods: We investigated the irisin-regulated lncRNA profile change in human mesenchymal stem cells (MSCs) using published whole transcriptome sequencing data. We predicted their potential targets and competitive endogenous RNA (ceRNA) prediction and analyzed their molecular functions using functional enrichment analysis.

Results: More differentially expressed lncRNAs (DElncRNAs) were observed in irisin-treated samples. The top irisin-induced lncRNAs were associated with OA or chondrogenic differentiation, including XIST, PAX8-AS1, CASC15, LINC01618, and DLX6-AS1. The DEGs co-expressed with DElncRNAs were enriched in skeletal system development, extracellular matrix (ECM) organization, cell adhesion, and inflammation associated pathways. Several lncRNAs likely acted as ceRNAs to regulate downstream mRNAs including ROR2 and SORBS1 in in OA or chondrogenic differentiation.

Conclusions: We demonstrate the global regulation of lncRNAs by irisin during chondrogenic differentiation of human MSCs. Further study is required to characterize the key irisin-regulated lncRNAs in chondrogenic differentiation.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
鸢尾素调控的lncRNA及其在人间质干细胞软骨分化中的潜在调控功能
目的:软骨分化失调与骨关节炎(OA)有关。肌动蛋白鸢尾素有益于 OA 的治疗,但其潜在机制尚未完全明了。长非编码 RNA(lncRNA)是软骨细胞分化的重要调节因子。本研究旨在探讨lncRNAs在介导鸢尾素诱导的软骨细胞分化中的作用:方法:我们利用已发表的全转录组测序数据研究了人间质干细胞(MSCs)中鸢尾素调控的lncRNA谱系变化。我们预测了它们的潜在靶标和竞争性内源性 RNA(ceRNA),并利用功能富集分析法分析了它们的分子功能:结果:在鸢尾素处理的样本中观察到了更多的差异表达lncRNAs(DElncRNAs)。鸢尾素诱导的最主要lncRNA与OA或软骨分化有关,包括XIST、PAX8-AS1、CASC15、LINC01618和DLX6-AS1。与DElncRNAs共表达的DEGs富集在骨骼系统发育、细胞外基质(ECM)组织、细胞粘附和炎症相关通路中。一些lncRNA可能作为ceRNA调控下游mRNA,包括OA或软骨分化过程中的ROR2和SORBS1:我们证明了鸢尾素在人类间充质干细胞软骨源分化过程中对lncRNAs的全局调控。我们还需要进一步的研究来确定在软骨源分化过程中鸢尾素调控的关键lncRNA。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Open Medicine
Open Medicine Medicine-General Medicine
CiteScore
3.00
自引率
0.00%
发文量
153
审稿时长
20 weeks
期刊介绍: Open Medicine is an open access journal that provides users with free, instant, and continued access to all content worldwide. The primary goal of the journal has always been a focus on maintaining the high quality of its published content. Its mission is to facilitate the exchange of ideas between medical science researchers from different countries. Papers connected to all fields of medicine and public health are welcomed. Open Medicine accepts submissions of research articles, reviews, case reports, letters to editor and book reviews.
期刊最新文献
Carboplatin combined with arsenic trioxide versus carboplatin combined with docetaxel treatment for LACC: A randomized, open-label, phase II clinical study. Iron in ventricular remodeling and aneurysms post-myocardial infarction. Predictive role of neuron-specific enolase and S100-β in early neurological deterioration and unfavorable prognosis in patients with ischemic stroke. Elevated serum miR-142-5p correlates with ischemic lesions and both NSE and S100β in ischemic stroke patients. Risk factors for progressive kyphosis after percutaneous kyphoplasty in osteoporotic vertebral compression fracture.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1