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Notch pathway is active during osteogenic differentiation of human bone marrow mesenchymal stem cells induced by pulsed electromagnetic fields

机译:在脉冲电磁场诱导的人骨髓间充质干细胞的骨骨髓间充质干细胞的成骨分化期间,凹口途径是活性的

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Pulsed electromagnetic fields (PEMFs) have been used to treat bone diseases, particularly nonunion healing. Although it is known that PEMFs promote the osteogenic differentiation of human mesenchymal stem cells (hMSCs), to date PEMF molecular mechanisms remain not clearly elucidated. The Notch signalling is a highly conserved pathway that regulates cell fate decisions and skeletal development. The aim of this study was to investigate if the known PEMF-induced osteogenic effects may involve the modulation of the Notch pathway. To this purpose, during in vitro osteogenic differentiation of bone marrow hMSCs in the absence and in the presence of PEMFs, osteogenic markers (alkaline phosphatase activity, osteocalcin and matrix mineralization), the messenger ribonucleic acid expression of osteogenic transcription factors (Runx2, Dlx5, Osterix) as well as of Notch receptors (Notch1-4), their ligands (Jagged1, Dll1 and Dll4) and nuclear target genes (Hes1, Hes5, Hey1, Hey2) were investigated. PEMFs stimulated all osteogenic markers and increased the expression of Notch4, Dll4, Hey1, Hes1 and Hes5 in osteogenic medium compared to control. In the presence of DAPT and SAHM1, used as Notch pathway inhibitors, the expression of the osteogenic markers, including Runx2, Dlx5, Osterix, as well as Hes1 and Hes5 were significantly inhibited, both in unexposed and PEMF-exposed hMSCs. These results suggest that activation of Notch pathway is required for PEMFs-stimulated osteogenic differentiation. These new findings may be useful to improve autologous cell-based regeneration of bone defects in orthopaedics.
机译:脉冲电磁场​​(PEMFS)已被用于治疗骨病,特别是非愈合。虽然已知PEMFS促进人间充质干细胞(HMSCs)的骨质发生分化,但迄今为止,PEMF分子机制仍未明确阐明。陷波信令是一种高度保守的途径,可调节细胞命运决策和骨骼发育。本研究的目的是研究已知的PEMF诱导的骨代原效应是否可能涉及凹口途径的调节。为此目的,在骨髓HMSC的体外成骨分化期间在没有和存在PEMF的存在下,骨质发生标记物(碱性磷酸酶活性,骨钙酶和基质矿化),骨代核核酸表达的表达核糖转录因子(RUNX2,DLX5, Ostorix)以及缺口受体(Notch1-4),它们的配体(Jagged1,DLL1和DLL4)和核靶基因(HES1,HES5,HEY1,HEY2)进行了研究。与对照相比,PEMFS刺激了所有成骨标志物,并增加了Notch4,DLL4,Hey1,HES1和HES5的表达。在存在DAPT和SAHM1的情况下,用作陷波途径抑制剂,在未曝光和PEMF暴露的HMSCs中显着抑制了骨质发生标记物的表达,包括RUNX2,DLX5,OSTERIX,以及HES5。这些结果表明,PEMFS刺激的骨质发生分化需要激活槽口途径。这些新发现可能有助于改善整形外科骨缺损的基于自体细胞的再生。

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