Ditchfield Caitlin, Price Joshua, Davis Edward T, Jones Simon W
Department of Inflammation and Ageing, College of Medicine and Health, University of Birmingham, Birmingham B15 2TT, UK.
NIHR Biomedical Research Centre, Birmingham B15 2TT, UK.
Biomolecules. 2025 Jun 6;15(6):829. doi: 10.3390/biom15060829.
Synovial inflammation is recognised as a pathological driver of osteoarthritis (OA), a degenerative joint disease involving cartilage degradation and joint pain. Since extracellular vesicles (EVs) have emerged as key mediators of cellular cross-talk, this study characterised synovial fluid EVs (SFEVs) in OA patients with varying disease severity and determined their functional effects on OA articular chondrocytes. Synovial fluid and articular cartilage were collected from patients undergoing knee surgery. SFEVs were isolated via ultracentrifugation and characterised by nanoparticle tracking analysis, ExoView, and Luminex analysis of protein cargo. Patients were stratified into mild/moderate- and severe-OA groups based on Oxford Knee Score and EQ5D. Chondrocytes were treated with SFEVs, and transcriptomic and secretome responses were analysed using RNA sequencing, Luminex, and ELISA. SFEVs from patients with severe OA were more abundant, smaller and exhibited increased tetraspanin expression. Synovial fluid and SFEVs induced distinct transcriptomic changes in chondrocytes. SFEVs from patients with severe OA promoted a pro-inflammatory and catabolic chondrocyte phenotype, with upregulation of , , , and , greater secretion of IL-6, MMP1, MMP3 and MMP13, and pro-nociceptive mediators (NGF and Substance P). These findings suggest that SFEVs may contribute to OA progression by exacerbating cartilage damage and promoting pain sensitisation.
滑膜炎症被认为是骨关节炎(OA)的病理驱动因素,骨关节炎是一种涉及软骨降解和关节疼痛的退行性关节疾病。由于细胞外囊泡(EVs)已成为细胞间通讯的关键介质,本研究对不同疾病严重程度的OA患者的滑液EVs(SFEVs)进行了表征,并确定了它们对OA关节软骨细胞的功能影响。从接受膝关节手术的患者中收集滑液和关节软骨。通过超速离心分离SFEVs,并通过纳米颗粒跟踪分析、ExoView和蛋白质载量的Luminex分析对其进行表征。根据牛津膝关节评分和EQ5D将患者分为轻度/中度OA组和重度OA组。用SFEVs处理软骨细胞,并使用RNA测序、Luminex和ELISA分析转录组和分泌组反应。重度OA患者的SFEVs数量更多、体积更小,且四跨膜蛋白表达增加。滑液和SFEVs在软骨细胞中诱导了不同的转录组变化。重度OA患者的SFEVs促进了软骨细胞的促炎和分解代谢表型,伴随着 、 、 和 的上调,IL-6、MMP1、MMP3和MMP13的分泌增加,以及促痛介质(NGF和P物质)的分泌增加。这些发现表明,SFEVs可能通过加剧软骨损伤和促进疼痛敏化而导致OA进展。