首页> 美国卫生研究院文献>American Journal of Translational Research >LncRNA H19 secreted by umbilical cord blood mesenchymal stem cells through microRNA-29a-3p/FOS axis for central sensitization of pain in advanced osteoarthritis
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LncRNA H19 secreted by umbilical cord blood mesenchymal stem cells through microRNA-29a-3p/FOS axis for central sensitization of pain in advanced osteoarthritis

机译:LNCRNA H19通过MicroRNA-29A-3P / FOS轴分泌的脐带血性间充质干细胞用于中央致敏性骨关节炎的中央致敏

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摘要

Objective: To explore the molecular mechanism of umbilical cord blood mesenchymal stem cells (UCBMSCs) in the treatment of advanced osteoarthritis pain. Methods: Normal healthy rats were selected to establish advanced osteoarthritis (OA) model, and the rats were randomly divided into control group, intravenous group, intracavitary group and intrathecal group. The intravenous group received intravenous injection of UCBMSCs, intracavitary group received intra-articular injection of UCBMSCs, and intrathecal group received subarachnoid injection of UCBMSCs. The pain behavior and serum pro-inflammatory factor levels were evaluated before and after treatment. microRNA-29a-3p and FOS mRNA in spinal dorsal horn was detected using qPCR, the phosphorylation of c-fos protein and NR1, NR2B, ERK and PKCg was detected using Western blot, and the level of LncRNA H19 was detected using qPCR. Results: LncRNA H19 was enriched in the exosomes of UCBMSCs. microRNA-29a-3p was the target gene of LncRNA H19, while FOS was the downstream target of microRNA-29a-3p. Pain and inflammation of rats in the intrathecal group improved best, and the phosphorylation levels of c-fos and NR1, NR2B, ERK and PKCg in the spinal dorsal horn of the intrathecal group decreased. LncRNA H19 regulated the central sensitization of astrocytes through microRNA-29a-3p/FOS axis. Conclusion: Intrathecal injection of umbilical cord blood mesenchymal stem cells can improve the pain and central sensitization of advanced osteoarthritis through LncRNA H19/microRNA-29a-3p/FOS axis.
机译:目的:研究的脐带血的分子机制间充质干晚期骨关节炎疼痛的治疗的细胞(UCBMSCs)。方法:选择正常健康大鼠建立先进骨关节炎(OA)模型,以及大鼠随机分为对照组,静脉内组,腔内组和鞘内基。静脉内组接受UCBMSCs的静脉注射,腔内组接受UCBMSCs的关节内注射和鞘内组接受UCBMSCs的蛛网膜下腔注射。疼痛行为,血清促炎症因子水平在治疗前后进行了评价。使用qPCR,c-fos蛋白,并使用Western blot检测NR1,NR2B,ERK和PKCg的磷酸化微小RNA-29A-3P和FOS mRNA的脊髓背角中检测到,并使用qPCR检测LncRNA H19的水平。结果:LncRNA H19在UCBMSCs的外来体富集。微小RNA-29A-3P是LncRNA H19的靶基因,同时FOS是微小RNA-29A-3P的下游靶标。疼痛和鞘内组大鼠炎症改善的最好的,和c-fos和NR1,NR2B,ERK和PKCg在鞘内组的脊髓背角的磷酸化水平降低。 LncRNA H19调节星形胶质细胞的通过微小RNA-29A-3P的中枢致敏/ FOS轴。结论:脐带血鞘内注射间充质干细胞可以通过提高H19 LncRNA /微小RNA-29A-3P / FOS轴的疼痛和骨关节炎先进中枢敏化。

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