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Treating Mesenchymal Stem Cells with Hepatocyte Growth Factor Enhances Cardiac Markers

机译:用肝细胞生长因子治疗间充质干细胞增强心脏标志物

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Human mesenchymal stem cells (hMSCs) derived from adult bone marrow are multipotent cells shown to have increased differentiation potential when cultured in reduced-oxygen (2% O_2) environments. Hepatocyte growth factor (HGF) is a mesodermal cytokine critical for organ formation during embryogenesis, including cardiogenesis. In this work, we tested the hypothesis that culturing hMSCs in reduced O_2 conditions with media supplemented with HGF increases the expression of cardiac myocyte markers. RT-PCR demonstrated expression of myocyte specific α-Actinin (ACTN2) and myocyte enhancement factor 2C (MEF2C) in reduced-O_2/HGF+ treated cells. Real time PCR showed an 11-fold increase in ACTN2 and 2-fold increase in MEF2C in reduced-O_2/HGF+ treated cells compared to hMSCs cultured in atmospheric-O_2/HGF- conditions. These results suggest that the combination of low oxygen and HGF may increase the cardiac differentiation capabilities of hMSCs.
机译:衍生自成人骨髓的人间充质干细胞(HMSCs)是当在减少氧(2%O_2)环境中培养时具有增加的分化电位的多能细胞。肝细胞生长因子(HGF)是胚胎发生期间的器官形成至关重要的中胚层细胞因子,包括心肌发生。在这项工作中,我们测试了培养HMSC在补充HGF的培养基中培养HMSC的假设增加了心肌细胞标记的表达。 RT-PCR在减少O_2 / HGF +处理细胞中显示了肌细胞特异性α-挥发蛋白(ACTN2)和肌细胞增强因子2C(MEF2C)的表达。与在大气 - O_2 / HGF条件下培养的HMSCs相比,实时PCR在减少的O_2 / HGF +处理细胞中,MEF2C的MEF2C中的actN2和2倍的增加11倍。这些结果表明,低氧和HGF的组合可以增加HMSC的心脏分化能力。

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