Departments of Pathology, Augusta University, Augusta, GA, 30912, USA.
Departments of Orthopaedic Surgery, Augusta University, Augusta, GA, 30912, USA.
Sci Rep. 2017 May 17;7(1):2029. doi: 10.1038/s41598-017-01905-y.
The pathogenesis of osteoarthritis (OA) is poorly understood, and therapeutic approaches are limited to preventing progression of the disease. Recent studies have shown that exosomes play a vital role in cell-to-cell communication, and pathogenesis of many age-related diseases. Molecular profiling of synovial fluid derived exosomal miRNAs may increase our understanding of OA progression and may lead to the discovery of novel biomarkers and therapeutic targets. In this article we report the first characterization of exosomes miRNAs from human synovial fluid. The synovial fluid exosomes share similar characteristics (size, surface marker, miRNA content) with previously described exosomes in other body fluids. MiRNA microarray analysis showed OA specific exosomal miRNA of male and female OA. Gene Ontology (GO) analysis and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis identified gender-specific target genes/signaling pathways. These pathway analyses showed that female OA specific miRNAs are estrogen responsive and target TLR (toll-like receptor) signaling pathways. Furthermore, articular chondrocytes treated with OA derived extracellular vesicles had decreased expression of anabolic genes and elevated expression of catabolic and inflammatory genes. In conclusion, synovial fluid exosomal miRNA content is altered in patients with OA and these changes are gender specific.
骨关节炎(OA)的发病机制尚不清楚,治疗方法仅限于预防疾病进展。最近的研究表明,外泌体在细胞间通讯和许多与年龄相关的疾病的发病机制中起着至关重要的作用。滑液来源的外泌体 miRNA 的分子谱分析可能会增加我们对 OA 进展的理解,并可能导致新的生物标志物和治疗靶点的发现。在本文中,我们报告了人类滑液中外泌体 miRNA 的首次特征描述。滑液外泌体具有与其他体液中先前描述的外泌体相似的特征(大小、表面标志物、miRNA 含量)。miRNA 微阵列分析显示男性和女性 OA 的 OA 特异性外泌体 miRNA。基因本体论(GO)分析和京都基因与基因组百科全书(KEGG)途径分析确定了性别特异性靶基因/信号通路。这些通路分析表明,女性 OA 特异性 miRNA 是雌激素反应性的,靶向 TLR( toll 样受体)信号通路。此外,用 OA 衍生的细胞外囊泡处理关节软骨细胞,可降低合成代谢基因的表达,升高分解代谢和炎症基因的表达。总之,OA 患者的滑液外泌体 miRNA 含量发生改变,且这些改变具有性别特异性。