Department of Rheumatology of the First Affiliated Hospital & the First Clinical College, Weifang Medical University, Weifang 261000, China.
Central Laboratory of the First Affiliated Hospital & the First Clinical College, Weifang Medical University, Weifang 261000, China.
Mediators Inflamm. 2023 Mar 31;2023:6818524. doi: 10.1155/2023/6818524. eCollection 2023.
Accumulating studies have implicated that circular RNAs (circRNAs) play vital roles in the pathogenesis of rheumatoid arthritis (RA). Dysregulation of macrophage polarization leads to immune homeostatic imbalance in RA. However, the altering effects and mechanisms of circRNAs on macrophages polarization and immune homeostatic balance remain largely unclear. We aimed to investigate the potential role of circRNA_17725 in RA. The high-throughput sequence was performed to identify the dysregulated circRNAs in RA. We confirmed the data by CCK-8, EdU, and Annexin V/PI staining to elucidate the proliferation and apoptosis. The expressions of M1/M2-associated markers were confirmed using real-time PCR and flow cytometry analysis. Luciferase reporter assay and RNA Binding Protein Immunoprecipitation (RIP) were used to demonstrate the underlying mechanism of circRNA_17725. The altering effect of circRNA_17725 on macrophages in vivo was evaluated using collagen-induced arthritis (CIA) mouse model. circRNA_17725 was demonstrated to be downregulated in peripheral blood mononuclear cells and CD14 monocytes from RA cases in contrast to healthy controls. The negative association between circRNA_17725 and the disease activity indexes (CRP, ESR, and DAS28) was observed, suggesting a vital role of circRNA_17725 in RA disease activity. Besides, after a coexpression analysis based on high-input sequencing and the bioinformatics analysis in MiRanda and TargetScan databases, a circRNA_17725-miR-4668-5p-FAM46C competing endogenous RNA (ceRNA) network was hypothesized. A series of cytology experiments have implicated that circRNA_17725 could inhibit the proliferation but enhance the apoptosis of macrophages. Decreased expression of TNF-, IL-1, and MMP-9 were observed in the supernatant of circRNA_17725-overexpressed Raw264.7 macrophages, implicating the inhibitory effect of circRNA_17725 on macrophage inflammatory mediators. Furthermore, circRNA_17725 could promote macrophage polarization towards M2 by targeting miR-4668-5p/FAM46C as a miRNA sponge. Additionally, circRNA_17725-overexpressed macrophages alleviated arthritis and protected against joint injuries and bone destruction by inducing macrophage polarization towards M2 in collagen-induced arthritis (CIA) mice. This study has suggested that circRNA_17725 regulated macrophage proliferation, apoptosis, inflammation, and polarization by sponging miR-4668-5p and upregulating FAM46C in RA.
越来越多的研究表明,环状 RNA(circRNAs)在类风湿关节炎(RA)的发病机制中发挥着重要作用。巨噬细胞极化的失调导致 RA 中免疫内稳态失衡。然而,circRNAs 对巨噬细胞极化和免疫内稳态平衡的改变作用及其机制在很大程度上仍不清楚。我们旨在研究 circRNA_17725 在 RA 中的潜在作用。通过高通量测序鉴定 RA 中失调的 circRNAs。我们通过 CCK-8、EdU 和 Annexin V/PI 染色来验证数据,以阐明增殖和凋亡情况。使用实时 PCR 和流式细胞术分析来确认 M1/M2 相关标记物的表达。使用荧光素酶报告基因测定和 RNA 结合蛋白免疫沉淀(RIP)来证明 circRNA_17725 的潜在机制。使用胶原诱导性关节炎(CIA)小鼠模型评估 circRNA_17725 对体内巨噬细胞的改变作用。与健康对照组相比,RA 患者外周血单核细胞和 CD14 单核细胞中发现 circRNA_17725 下调。circRNA_17725 与疾病活动指标(CRP、ESR 和 DAS28)呈负相关,表明 circRNA_17725 在 RA 疾病活动中具有重要作用。此外,基于高通量测序的共表达分析和 MiRanda 和 TargetScan 数据库中的生物信息学分析,提出了 circRNA_17725-miR-4668-5p-FAM46C 竞争性内源 RNA(ceRNA)网络。一系列细胞学实验表明,circRNA_17725 可抑制巨噬细胞的增殖,但可促进其凋亡。在过表达 circRNA_17725 的 Raw264.7 巨噬细胞的上清液中观察到 TNF-α、IL-1 和 MMP-9 表达降低,表明 circRNA_17725 对巨噬细胞炎性介质具有抑制作用。此外,circRNA_17725 可通过作为 miRNA 海绵靶向 miR-4668-5p/FAM46C 来促进巨噬细胞向 M2 极化。此外,在胶原诱导性关节炎(CIA)小鼠中,过表达 circRNA_17725 可通过诱导巨噬细胞向 M2 极化来减轻关节炎并保护关节损伤和骨破坏。这项研究表明,circRNA_17725 通过在 RA 中海绵吸附 miR-4668-5p 和上调 FAM46C 来调节巨噬细胞增殖、凋亡、炎症和极化。