乌头汤调控lncRNA MALAT1改善骨关节炎软骨细胞铁代谢紊乱机制研究OA
Mechanism Study on Wutou Decoction Regulating lncRNA MALAT1 to Improve Iron Metabolism Disorder in Chondrocytes of Osteoarthritis
目的:探讨乌头汤是否通过lncRNA MALAT1调控作用调节白细胞介素-1β(IL-1β)诱导的软骨细胞炎症铁代谢紊乱.方法:提取20只雄性SPF级C57BL/6小鼠的双侧膝关节软骨细胞用于体外培养;用10 ng/mL的IL-1β作用24h诱导体外软骨细胞炎症模型,构建lncRNA MALAT1过表达细胞;将软骨细胞分为空白组、模型组、乌头汤组、lncRNA MALAT1过表达组、lncRNA MALAT1过表达+乌头汤组.使用Real-time PCR技术分别检测lncRNA MALAT1在各组软骨细胞中的相对表达水平,Western blot方法检测MMP 13、GPX4、ACSL4和COX2在各组软骨细胞中的蛋白表达含量.结果:Real-time PCR结果显示,经IL-1β诱导的软骨细胞炎症模型lncRNAMALAT1的表达量显著升高(P<0.05),Western blot结果显示,与空白组相比,模型组中MMP 13、ACSL4 和COX2 的表达量均呈现出上升的趋势(P<0.05),GPX4表达量下降(P<0.05);与lncRNA MALAT1过表达组相比,lncRNA MALAT1过表达+乌头汤组,MMP13、ACSL4和COX2表达量降低(P<0.05),GPX4表达量升高(P<0.05);与模型组相比,乌头汤组表现出MMP13、ACSL4和COX2表达量降低(P<0.05),GPX4表达量升高的趋势(P<0.05).结论:乌头汤能够通过调控lncRNA MALAT1减少MMP13、ACSL4和COX2的表达及增强GPX4的蛋白表达量,调控OA软骨细胞铁代谢紊乱的过程,延缓软骨细胞退变的进程.
Objective:To investigate whether Wutou Decoction regulates interleukin-1β(IL-1β)-induced inflammatory iron metabolism disorder in chondrocytes through the regulatory role of lncRNA MALAT1.Methods:Chondrocytes were extracted from the bilateral knee joints of 20 male SPF-grade C57BL/6 mice for in vitro culture.An in vitro chondrocyte inflammation model was induced by treatment with 10 ng/mL IL-1β for 24 hours,and lncRNA MALAT1 overexpressing cells were constructed.The chondrocytes were divided into five groups:blank group,model group,Wutou Decoction group,lncRNA MALAT1 overexpression group and lncRNA MALAT1 overexpression+Wutou Decoction group.Real-time PCR was used to detect the relative expression level of lncRNA MALAT1 in chondrocytes of each group.Western blot was used to determine the protein expression levels of MMP13,GPX4,ACSL4,and COX2 in chondrocytes of each group.Results:Real-time PCR results showed that the expression of lncRNA MALAT1 was significantly increased in the IL-1β-induced chondrocyte inflammation model(P<0.05).Western blot results showed that,compared with the blank group,the model group showed an upward trend in the expression levels of MMP13,ACSL4 and COX2,while the expression level of GPX4 decreased(P<0.05).Compared with the lncRNA MALAT1 overexpression group,the lncRNA MALAT1 overexpression+Wutou Decoction group had decreased expression levels of MMP13,ACSL4,and COX2,and increased expression level of GPX4(P<0.05).Compared with the model group,the Wutou Decoction group showed decreased expression levels of MMP13,ACSL4,and COX2(P<0.05),and an increasing trend in GPX4 expression(P<0.05).Conclusion:Wutou Decoction can reduce the expressions of MMP13,ACSL4,and COX2,and enhance the protein expression level of GPX4 by regulating lncRNA MALAT1,thereby regulating the process of iron metabolism disorder in OA chondrocytes and delaying the progression of chondrocyte degeneration.
兰书洁;游伟明;王宇尧;仲卫红
福建中医药大学康复医学院,福建 福州 350122福建中医药大学中西医结合学院/中西医结合研究院,福建 福州 350122||福建省中西医结合老年性疾病重点实验室,福建 福州 350122福建中医药大学中西医结合学院/中西医结合研究院,福建 福州 350122||福建省中西医结合老年性疾病重点实验室,福建 福州 350122福建中医药大学附属康复医院,福建 福州 350003||福建省康复技术重点实验室,福建 福州 350003
医药卫生
骨关节炎乌头汤铁代谢紊乱软骨细胞lncRNA MALAT1
osteoarthritisWutou Decoctioniron metabolism disorderchondrocytelncRNA MALAT1
《中医康复》 2026 (6)
38-44,7
福建室开放课题省康复技术重点试验(XKF2023001)福建中医药大学中医骨伤科学学科开放课题(XGS2023007)
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