首页> 美国卫生研究院文献>Analytical Cellular Pathology : the Journal of the European Society for Analytical Cellular Pathology >MicroRNA-378 Promotes Osteogenesis-Angiogenesis Coupling in BMMSCs for Potential Bone Regeneration
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MicroRNA-378 Promotes Osteogenesis-Angiogenesis Coupling in BMMSCs for Potential Bone Regeneration

机译:MicroRNA-378促进骨髓间充质干细胞中成骨-血管生成的耦合用于潜在的骨再生。

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摘要

Bone tissue regeneration was closely associated with osteogenesis and angiogenesis. The harmonious regulation of osteogenetic and angiogenic growth factors would enhance bone regeneration, while the imbalance of that would lead to local excessive bone formation or vascular mass due to exogenous delivery. Therefore, microRNA is believed to regulate multiple metabolism progress through endogenous signaling pathways on the gene level. In this work, we identified microRNA 378 as a positive regulator of osteogenesis and angiogenesis simultaneously and also observed an increase of microRNA 378 than control in human bone marrow mesenchymal stem cells (hBMMSCs) after osteoblast induction. Besides, osteogenetic and angiogenic gene expression increased simultaneously after overexpression of microRNA 378. Moreover, alizarin red staining and alkaline phosphatase (ALP) staining enhanced, and secretion of vascular endothelial growth factor (VEGF) increased. In this way, we believed miR378 was an ideal target to osteogenesis-angiogenesis coupling for bone regeneration, which provides a potential tool for the gene therapy of bone regeneration.
机译:骨组织再生与成骨和血管生成密切相关。成骨和血管生成生长因子的协调调节将增强骨再生,而其失衡将由于外源性递送而导致局部过量的骨形成或血管质量。因此,相信微小RNA通过基因水平上的内源性信号传导途径调节多种代谢进程。在这项工作中,我们将microRNA 378同时鉴定为成骨和血管生成的正向调节剂,并且还观察到成骨细胞诱导后人骨髓间充质干细胞(hBMMSCs)中microRNA 378的表达比对照增加。此外,microRNA 378过表达后,成骨和血管生成基因的表达同时增加。此外,茜素红染色和碱性磷酸酶(ALP)染色增强,血管内皮生长因子(VEGF)的分泌增加。通过这种方式,我们认为miR378是骨再生的成骨-血管生成偶联的理想靶标,这为骨再生的基因治疗提供了潜在的工具。

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