{"title":"Synovial fluid transcriptome dynamics in osteoarthritis progression: Implications in pathogenesis","authors":"Rinkle Sharma, Diksha Rana, Rahul Kumar, Sakshi Narula, Alpa Chaudhary, Bhavneet Kaur, Khushpreet Kaur, Mandeep Singh Dhillon, Devendra Chouhan, Uttam Chand Saini, Sadhna Sharma, Jyotdeep Kaur, Indu Verma","doi":"10.1101/2024.06.24.600143","DOIUrl":null,"url":null,"abstract":"Background: Osteoarthritis, a degenerative joint disease associated with various pathological manifestations in the joint including cartilage loss, alterations in subchondral bone and synovial inflammation. Objective: This study aimed to elucidate the transcriptional and molecular changes in synovial fluid associated with OA progression, focusing on differential gene expression and pathway enrichment across OA grades. Methodology: Patients with different OA grades were recruited from PGIMER, Chandigarh, following the KL classification. Microarray analysis was conducted to study the transcriptional profiles in different OA grades using a fold-change (FC) cutoff of 2 and a p-value cutoff of 0.05, followed by pathway analysis performed using GSEA and STRING database. Selected genes from microarray and pathway analysis were validated using qRT-PCR. Results: Microarray analysis reveals distinct gene expression patterns corresponding to different OA stages (KL grade 2 to KL grade 4). Notably, the upregulation of AMTN and DKK2, alongside the downregulation of MSLN, highlighted their roles in pathological mineralization and disrupted bone remodeling in OA. Pathway enrichment analysis revealed significant changes in immune response, inflammation related pathways and cellular processes such as autophagy and programmed cell death, indicating their involvement in disease progression. Furthermore, mitochondrial dysfunction and impaired autophagy were linked to increased inflammation in advanced OA. Conclusion: These findings suggest that targeting mineralization and inflammatory pathways could offer novel therapeutic avenues for OA management.","PeriodicalId":501471,"journal":{"name":"bioRxiv - Pathology","volume":"190 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"bioRxiv - Pathology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/2024.06.24.600143","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Osteoarthritis, a degenerative joint disease associated with various pathological manifestations in the joint including cartilage loss, alterations in subchondral bone and synovial inflammation. Objective: This study aimed to elucidate the transcriptional and molecular changes in synovial fluid associated with OA progression, focusing on differential gene expression and pathway enrichment across OA grades. Methodology: Patients with different OA grades were recruited from PGIMER, Chandigarh, following the KL classification. Microarray analysis was conducted to study the transcriptional profiles in different OA grades using a fold-change (FC) cutoff of 2 and a p-value cutoff of 0.05, followed by pathway analysis performed using GSEA and STRING database. Selected genes from microarray and pathway analysis were validated using qRT-PCR. Results: Microarray analysis reveals distinct gene expression patterns corresponding to different OA stages (KL grade 2 to KL grade 4). Notably, the upregulation of AMTN and DKK2, alongside the downregulation of MSLN, highlighted their roles in pathological mineralization and disrupted bone remodeling in OA. Pathway enrichment analysis revealed significant changes in immune response, inflammation related pathways and cellular processes such as autophagy and programmed cell death, indicating their involvement in disease progression. Furthermore, mitochondrial dysfunction and impaired autophagy were linked to increased inflammation in advanced OA. Conclusion: These findings suggest that targeting mineralization and inflammatory pathways could offer novel therapeutic avenues for OA management.
背景:骨关节炎是一种退行性关节疾病,与关节内的各种病理表现有关,包括软骨损失、软骨下骨改变和滑膜炎症。研究目的本研究旨在阐明滑液中与 OA 进展相关的转录和分子变化,重点关注不同 OA 等级的差异基因表达和通路富集。研究方法:根据 KL 分级,从昌迪加尔的 PGIMER 招募了不同 OA 等级的患者。使用折叠变化(FC)截止值 2 和 p 值截止值 0.05 进行微阵列分析,研究不同 OA 等级的转录概况,然后使用 GSEA 和 STRING 数据库进行通路分析。利用 qRT-PCR 对微阵列和通路分析中的部分基因进行了验证。结果微阵列分析显示了与不同 OA 阶段(KL 2 级到 KL 4 级)相对应的不同基因表达模式。值得注意的是,AMTN和DKK2的上调以及MSLN的下调突显了它们在OA病理矿化和骨重塑过程中的作用。通路富集分析显示,免疫反应、炎症相关通路以及自噬和程序性细胞死亡等细胞过程发生了显著变化,表明它们参与了疾病的进展。此外,线粒体功能障碍和自噬功能受损与晚期 OA 中炎症的增加有关。结论这些研究结果表明,针对矿化和炎症途径可为治疗 OA 提供新的治疗途径。