首页> 美国卫生研究院文献>International Journal of Molecular Sciences >CXCL13 Promotes the Effect of Bone Marrow Mesenchymal Stem Cells (MSCs) on Tendon-Bone Healing in Rats and in C3HIOT1/2 Cells
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CXCL13 Promotes the Effect of Bone Marrow Mesenchymal Stem Cells (MSCs) on Tendon-Bone Healing in Rats and in C3HIOT1/2 Cells

机译:CXCL13促进骨髓间充质干细胞(MSC)对大鼠和C3HIOT1 / 2细胞的腱-骨愈合的影响。

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摘要

Objectives: Mesenchymal stem cells (MSCs) are potential effective therapy for tissue repair and bone regeneration. In present study, the effects of CXC chemokine ligand-13 (CXCL13) were evaluated on tendon-bone healing of rats. Methods: Tendon bone healing of the rat model was established and biomechanical testing was performed at 2, 4, 8 weeks after surgery. Murine mesenchymal cell line (C3HIOT1/2 cells) was cultured. The expression of miRNA-23a was detected by real-time PCR. The protein expression of ERK1/2, JNK and p38 was detected by western blotting. MiR-23a mimic and inhibitor were used to overexpress or silence the expression of miR-23a. Results: MSCs significantly elevated the levels of ultimate load to failure, stiffness and stress in specimens of rats, the effects of which were enhanced by CXCL13. The expression of miR-23a was down-regulated and the protein of ERK1/2 level was up-regulated by CXCL13 treatment in both in vivo and in vitro experiments. ERK1/2 expression was elevated by overexpression of miR-23a and reduced by miR-23a inhibitor. Conclusions: These findings revealed that CXCL13 promoted the tendon-bone healing in rats with MSCs treatment, and implied that the activation of ERK1/2 via miR-23a was involved in the process of MSCs treated bone regeneration.
机译:目的:间充质干细胞(MSCs)是用于组织修复和骨骼再生的潜在有效疗法。在本研究中,评估了CXC趋化因子配体13(CXCL13)对大鼠腱-骨愈合的影响。方法:建立大鼠模型的肌腱骨愈合,并在术后2、4、8周进行生物力学测试。培养小鼠间充质细胞系(C3HIOT1 / 2细胞)。通过实时PCR检测miRNA-23a的表达。 Western blotting检测ERK1 / 2,JNK和p38蛋白的表达。使用MiR-23a模拟物和抑制剂来过表达或沉默miR-23a的表达。结果:MSC显着提高了大鼠标本的破坏,僵硬和应力极限负荷水平,而CXCL13增强了这种效应。在体内和体外实验中,CXCL13处理均能下调miR-23a的表达,并上调ERK1 / 2的表达。 ERK1 / 2表达由于miR-23a的过表达而升高,而因miR-23a抑制剂而降低。结论:这些发现表明,CXCL13促进了MSCs治疗大鼠的腱骨愈合,并暗示通过miR-23a激活ERK1 / 2参与了MSCs治疗的骨再生过程。

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