首页|METTL3通过mRNA m6A甲基化促进类风湿关节炎滑膜成纤维细胞增殖、迁移及分泌炎症因子

METTL3通过mRNA m6A甲基化促进类风湿关节炎滑膜成纤维细胞增殖、迁移及分泌炎症因子

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目的 探讨甲基转移酶样3(METTL3)对类风湿关节炎(RA)滑膜成纤维细胞增殖、迁移及分泌炎症因子的作用及机制.方法 本研究纳入类风湿关节炎及骨关节炎患者各25 例,留取滑膜组织,分别用RT-qPCR及免疫组化法检测METTL3 表达水平,ELISA检测RNA m6A浓度;分离培养RA滑膜成纤维细胞,分为NC组、hi-METTL3(过表达MET-TL3)组、si-METTL3(敲低METTL3)组、STM2457(METTL3 抑制剂)干预组,用CCK-8 法检测细胞增殖,流式细胞仪检测细胞凋亡、ELISA检测细胞培养上清液白介素-6(IL-6)、白介素-17A(IL-17A)、肿瘤坏死因子-κB 活化受体配体(RANKL)、骨保护素(OPG)的浓度.结果 与骨关节炎滑膜组织相比,RA 滑膜组织 RNA m6A 表达显著增高(P<0.05),METTL3 的表达显著增高(P<0.05).过表达MET-TL3 后,滑膜成纤维细胞m6A表达增加,细胞增殖、迁移能力显著提高,凋亡无明显变化,分泌细胞因子 IL-6、RANKL显著增加,OPG 显著减少(P<0.05).干扰 METTL3 表达后,滑膜成纤维细胞m6A表达减少,细胞增殖、迁移显著减低,分泌细胞因子IL-6、RANKL显著降低,OPG显著增高(P<0.05);使用 METTL3 抑制剂 STM2457 干预后,滑膜成纤维细胞增殖、迁移显著减低,分泌细胞因子IL-6、RANKL显著降低,OPG显著增高(P<0.05);各组表达IL-17A无显著差异.结论 METTL3 可能通过RNA m6A甲基化修饰促进RA滑膜成纤维细胞增殖、迁移及促进IL-6、RANKL的表达,抑制OPG的表达.
METTL3 promotes proliferation,migration,and secretion of inflammatory factors by mRNA m6A methylation in rheumatoid arthritis synovial fibroblasts
Objective To investigate the effect and mechanism of methyltransferase-like 3(METTL3)on the pro-liferation,migration,and secretion of inflammatory factors by synovial fibroblasts from rheumatoid arthritis(RA).Methods The expression of METTL3 in synovial tissue(SF)from 25 patients with rheumatoid arthritis and 25 pa-tients with osteoarthritis was detected by RT-qPCR and immunohistochemistry,respectively.The concentration of RNA m6A was detected by ELISA.RA synovial fibroblasts were isolated and cultured,and divided into NC(nor-mal control)group,hi-METTL3(overexpression of METTL3)group,si-METTL3(knock-down METTL3)group,and STM2457(METTL3 specific inhibitor)intervention group.Cell proliferation was detected by CCK-8 method.Apoptosis was detected by flow cytometry.And the concentrations of interleukin-6(IL-6),interleukin-17A(IL-17A),receptor activator of nuclear factor-kappa B ligand(RANKL),and osteoprotegerin(OPG)in the superna-tant of cell culture were detected by ELISA.Results Compared with synovial tissue of osteoarthritis,the expres-sion of mRNA m6A and METTL3 in synovial tissue of RA significantly increased(P<0.05).After overexpression of METTL3,the expression of m6A in synovial fibroblasts increased.The proliferation and migration abilities of SF in hi-METTL3 group were significantly improved,and their apoptosis did not change significantly.The secretion of cytokines IL-6 and RANKL of SF in hi-METTL3 group significantly increased,while the OPG significantly de-creased(P<0.05).After interfering with METTL3 expression,the expression of m6A in synovial fibroblasts de-creased.Cell proliferation and migration of SF in siMETTL3 group significantly decreased.The secretion of cyto-kines IL-6 and RANKL significantly decreased,and OPG significantly increased(P<0.05).After intervention with METTL3 inhibitor STM2457,the proliferation and migration of synovial fibroblasts were significantly reduced,and the secretion of cytokines IL-6 and RANKL significantly reduced,and OPG significantly increased(P<0.05).There was no significant difference in the expression of IL-17A among each group.Conclusion METTL3 may promote the proliferation and migration of RA synovial fibroblasts,enhance the expression of IL-6 and RANKL,and inhibit the expression of OPG through RNA m6A methylation modification.

methyltransferase like 3methylationrheumatoid arthritisproliferationmigrationinflammatory factors

李娟、蒋扬青、沈瑞明、李国铨、王敏、徐逢皇

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海南医学院第一附属医院风湿免疫科,海口 570102

甲基转移酶样3 甲基化 类风湿关节炎 增殖 迁移 炎症因子

海南省自然科学基金青年基金

820QN400

2024

安徽医科大学学报
安徽医科大学

安徽医科大学学报

CSTPCD北大核心
影响因子:1.095
ISSN:1000-1492
年,卷(期):2024.59(4)
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