首页> 美国卫生研究院文献>Oncotarget >Platelet-derived growth factor receptor-alpha positive cardiac progenitor cells derived from multipotent germline stem cells are capable of cardiomyogenesis in vitro and in vivo
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Platelet-derived growth factor receptor-alpha positive cardiac progenitor cells derived from multipotent germline stem cells are capable of cardiomyogenesis in vitro and in vivo

机译:来自多能干系干细胞的血小板衍生生长因子受体-α阳性心脏祖细胞能够在体外和体内进行心肌发生

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摘要

Cardiac cell therapy has the potential to revolutionize treatment of heart diseases, but its success hinders on the development of a stem cell therapy capable of efficiently producing functionally differentiated cardiomyocytes. A key to unlocking the therapeutic application of stem cells lies in understanding the molecular mechanisms that govern the differentiation process. Here we report that a population of platelet-derived growth factor receptor alpha (PDGFRA) cells derived from mouse multipotent germline stem cells (mGSCs) were capable of undergoing cardiomyogenesis in vitro. Cells derived in vitro from PDGFRA positive mGSCs express significantly higher levels of cardiac marker proteins compared to PDGFRA negative mGSCs. Using Pdgfra shRNAs to investigate the dependence of Pdgfra on cardiomyocyte differentiation, we observed that Pdgfra silencing inhibited cardiac differentiation. In a rat myocardial infarction (MI) model, transplantation of a PDGFRAenriched cell population into the rat heart readily underwent functional differentiation into cardiomyocytes and reduced areas of fibrosis associated with MI injury. Together, these results suggest that mGSCs may provide a unique source of cardiac stem/progenitor cells for future regenerative therapy of damaged heart tissue.
机译:心脏细胞疗法具有彻底改变心脏病治疗的潜力,但其成功阻碍了能够有效产生功能分化型心肌细胞的干细胞疗法的发展。开启干细胞治疗应用的关键在于了解控制分化过程的分子机制。在这里我们报告从小鼠专能生殖系干细胞(mGSCs)衍生的血小板衍生生长因子受体α(PDGFRA)细胞群体能够在体外进行心肌发生。与PDGFRA阴性mGSC相比,PDGFRA阳性mGSC的体外细胞表达的心脏标志物蛋白水平高得多。使用Pdgfra shRNA来研究Pdgfra对心肌细胞分化的依赖性,我们观察到Pdgfra沉默抑制了心脏分化。在大鼠心肌梗塞(MI)模型中,将富含PDGFRA的细胞群移植到大鼠心脏中,很容易将其功能分化为心肌细胞,并减少与MI损伤相关的纤维化区域。总之,这些结果表明,mGSC可能为心脏受损的未来组织的再生治疗提供心脏干/祖细胞的独特来源。

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