Synovial Dysregulation in Ankle Osteoarthritis: Molecular Insights and Pathogenetic Pathways.

IF 2.1 3区 医学 Q2 ORTHOPEDICS
Julia Matthias, Sara Buckley, Michael David, Cheryl L Ackert-Bicknell, Joshua A Metzl, Daniel K Moon, Courtney Miller, Michael J Zuscik, Kenneth J Hunt
{"title":"Synovial Dysregulation in Ankle Osteoarthritis: Molecular Insights and Pathogenetic Pathways.","authors":"Julia Matthias, Sara Buckley, Michael David, Cheryl L Ackert-Bicknell, Joshua A Metzl, Daniel K Moon, Courtney Miller, Michael J Zuscik, Kenneth J Hunt","doi":"10.1002/jor.70016","DOIUrl":null,"url":null,"abstract":"<p><p>Osteoarthritis of the ankle is a debilitating condition affecting nearly 20% of adults in the United States. The tissue, cellular, and molecular basis of this disease remains poorly understood, particularly the role of the synovial membrane. This prospective case-control study examined the gene expression profile of synovial tissue in ankle osteoarthritis to uncover biological pathways altered in the disease. Synovial biopsies were obtained from twenty-six patients with ankle osteoarthritis undergoing joint replacement and eight patients with minimal or no evidence of osteoarthritis. Bulk RNA-sequencing and differential gene expression analysis were performed, followed by biological pathway enrichment, unsupervised cluster, and network-based analysis. Synovium from ankle osteoarthritis patients showed distinct gene expression patterns compared to controls, with enrichment in pathways related to extracellular matrix remodeling and tissue morphogenesis. Age and a prior history of ankle fracture were identified as significant factors influencing the transcriptomic profile of osteoarthritic synovium. After accounting for these variables, transcriptomic clustering perfectly distinguished osteoarthritic from non-osteoarthritic synovium and revealed upregulation of pathways involved in muscle development, neural signaling, immune response, and carbohydrate metabolism. Conversely, pathways related to ribosome production, protein synthesis, and cellular signaling were downregulated. Multiple WNT signaling pathways remained significantly enriched in osteoarthritic ankle synovium. This study identifies a distinct gene expression profile in the synovium of ankle osteoarthritis patients, highlighting key molecular pathways possibly involved in disease progression. These findings provide valuable insights into the molecular mechanisms driving ankle osteoarthritis and have the potential to inform the development of novel targeted therapeutic strategies.</p>","PeriodicalId":16650,"journal":{"name":"Journal of Orthopaedic Research®","volume":" ","pages":""},"PeriodicalIF":2.1000,"publicationDate":"2025-07-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Orthopaedic Research®","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1002/jor.70016","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ORTHOPEDICS","Score":null,"Total":0}
引用次数: 0

Abstract

Osteoarthritis of the ankle is a debilitating condition affecting nearly 20% of adults in the United States. The tissue, cellular, and molecular basis of this disease remains poorly understood, particularly the role of the synovial membrane. This prospective case-control study examined the gene expression profile of synovial tissue in ankle osteoarthritis to uncover biological pathways altered in the disease. Synovial biopsies were obtained from twenty-six patients with ankle osteoarthritis undergoing joint replacement and eight patients with minimal or no evidence of osteoarthritis. Bulk RNA-sequencing and differential gene expression analysis were performed, followed by biological pathway enrichment, unsupervised cluster, and network-based analysis. Synovium from ankle osteoarthritis patients showed distinct gene expression patterns compared to controls, with enrichment in pathways related to extracellular matrix remodeling and tissue morphogenesis. Age and a prior history of ankle fracture were identified as significant factors influencing the transcriptomic profile of osteoarthritic synovium. After accounting for these variables, transcriptomic clustering perfectly distinguished osteoarthritic from non-osteoarthritic synovium and revealed upregulation of pathways involved in muscle development, neural signaling, immune response, and carbohydrate metabolism. Conversely, pathways related to ribosome production, protein synthesis, and cellular signaling were downregulated. Multiple WNT signaling pathways remained significantly enriched in osteoarthritic ankle synovium. This study identifies a distinct gene expression profile in the synovium of ankle osteoarthritis patients, highlighting key molecular pathways possibly involved in disease progression. These findings provide valuable insights into the molecular mechanisms driving ankle osteoarthritis and have the potential to inform the development of novel targeted therapeutic strategies.

踝关节骨关节炎的滑膜失调:分子观察和发病途径。
踝关节骨关节炎是一种使人衰弱的疾病,影响着美国近20%的成年人。这种疾病的组织、细胞和分子基础仍然知之甚少,特别是滑膜的作用。这项前瞻性病例对照研究检查了踝关节骨关节炎滑膜组织的基因表达谱,以揭示该疾病改变的生物学途径。对26例接受关节置换术的踝关节骨关节炎患者和8例轻度或无骨关节炎证据的患者进行了滑膜活检。进行了大量rna测序和差异基因表达分析,随后进行了生物途径富集,无监督聚类和基于网络的分析。与对照组相比,踝关节骨关节炎患者的滑膜显示出不同的基因表达模式,与细胞外基质重塑和组织形态发生相关的通路富集。年龄和踝关节骨折史被确定为影响骨关节炎滑膜转录组谱的重要因素。在考虑了这些变量后,转录组聚类完全区分了骨关节炎和非骨关节炎滑膜,并揭示了涉及肌肉发育、神经信号、免疫反应和碳水化合物代谢的途径上调。相反,与核糖体产生、蛋白质合成和细胞信号传导相关的途径被下调。骨性关节炎踝关节滑膜中多种WNT信号通路仍显著富集。本研究确定了踝关节骨关节炎患者滑膜中独特的基因表达谱,突出了可能参与疾病进展的关键分子途径。这些发现为踝关节骨关节炎的分子机制提供了有价值的见解,并有可能为开发新的靶向治疗策略提供信息。
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 求助全文
来源期刊
Journal of Orthopaedic Research®
Journal of Orthopaedic Research® 医学-整形外科
CiteScore
6.10
自引率
3.60%
发文量
261
审稿时长
3-6 weeks
期刊介绍: The Journal of Orthopaedic Research is the forum for the rapid publication of high quality reports of new information on the full spectrum of orthopaedic research, including life sciences, engineering, translational, and clinical studies.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信