Department of Orthopedics, Affiliated Hospital of Zunyi Medical University, Zunyi, China.
Key Laboratory of Cell Engineering of Guizhou Province, Affiliated Hospital of Zunyi Medical University, Zunyi, China.
Artif Cells Nanomed Biotechnol. 2023 Dec;51(1):242-254. doi: 10.1080/21691401.2023.2185627.
Osteoarthritis (OA) is a multi-factorial chronic joint disease mainly identified by synovial inflammation, cartilage damage, and degeneration. Our study applied bioinformatics analysis to uncover the immunity in OA and tried to explore the underlying immune-related molecular mechanism. First, OA-related gene-expression profiling data were retrieved from GEO database. Then, we analysed a series of datadata with using the xCell algorithm, GEO2R, enrichment analysis of SangerBox website, CytoHubba, ROC logistic regression and correlation analysis. Finally, Nine infiltrating immune cells with differential abundance between OA and normal samples were obtained. There were 42 IODEGs in OA, and their functions were associated with immune cells and corresponding biological processes. Moreover, 5 hub genes, including GREM1, NRP1, VEGFA, FYN and IL6R, were identified. Correlation analysis demonstrated that NRP1 was negatively associated with NKT cells, NRP1 and GREM1 were positively associated with aDC, VEGFA was positively associated with CD8+ naïve T cells, while VEGFA, FYN and IL6R were negatively associated with Macrophages M1. The 5 hub genes could be employed as effective diagnostic biomarkers for OA. In addition, they may participate in OA pathogenesis interactions with infiltrating immune cells.
骨关节炎(OA)是一种多因素的慢性关节疾病,主要表现为滑膜炎症、软骨损伤和退变。我们的研究应用生物信息学分析来揭示 OA 中的免疫,并试图探索潜在的免疫相关分子机制。首先,从 GEO 数据库中检索到与 OA 相关的基因表达谱数据。然后,我们使用 xCell 算法、GEO2R、SangerBox 网站的富集分析、CytoHubba、ROC 逻辑回归和相关性分析对一系列数据进行了分析。最后,获得了在 OA 和正常样本之间存在差异丰度的 9 种浸润性免疫细胞。在 OA 中有 42 个 IODEGs,其功能与免疫细胞和相应的生物过程有关。此外,还鉴定出 5 个枢纽基因,包括 GREM1、NRP1、VEGFA、FYN 和 IL6R。相关性分析表明,NRP1 与 NKT 细胞呈负相关,NRP1 和 GREM1 与 aDC 呈正相关,VEGFA 与 CD8+naive T 细胞呈正相关,而 VEGFA、FYN 和 IL6R 与巨噬细胞 M1 呈负相关。这 5 个枢纽基因可以作为 OA 的有效诊断生物标志物。此外,它们可能与浸润性免疫细胞相互作用参与 OA 发病机制。