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Generation of murine induced pluripotent stem cells by using high-density distributed electrodes network

机译:利用高密度分布电极网络生成鼠诱导性多能干细胞

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摘要

This study reports a robust method of gene transfection in a murine primary cell model by using a high-density electrodes network (HDEN). By demonstrating high cell viability after gene transfection and successful expression of transgenes including fluorescent proteins, the HDEN device shows great promise as a solution in which reprogramming efficiency using non-viral induction for generation of murine induced pluripotent stem cells (iPSCs) is optimized. High and steady transgene expression levels in host cells of iPSCs can be demonstrated using this method. Moreover, the HDEN device achieved successful gene transfection with a low voltage of less than 180 V while requiring relatively low cell numbers (less than 1.5 × 104 cells). The results are comparable to current conventional methods, demonstrating a reasonable fluorescent-plasmid transfection rate (42.4% in single transfection and 24.5% in triple transfection) and high cell viability of over 95%. The gene expression levels of each iPSC factor was measured to be over 10-fold higher than that reported in previous studies using a single mouse embryonic fibroblast cell. Our results demonstrate that the generation of iPSCs using HDEN transfection of plasmid DNA may be a feasible and safe alternative to using viral transfection methods in the near future.
机译:这项研究报告了通过使用高密度电极网络(HDEN)在鼠原代细胞模型中进行基因转染的可靠方法。通过证明基因转染后细胞的高存活力以及包括荧光蛋白在内的转基因的成功表达,HDEN装置作为一种解决方案具有广阔的前景,在该解决方案中,利用非病毒诱导产生鼠诱导性多能干细胞(iPSC)的重编程效率得到了优化。使用这种方法可以证明iPSC宿主细胞中高水平和稳定的转基因表达水平。此外,HDEN设备在小于180 V的低电压下成功实现了基因转染,同时需要相对较少的细胞数量(小于1.5×××10 4 细胞)。结果与目前的常规方法相当,证明了合理的荧光质粒转染率(单次转染为42.4%,三次转染为24.5%),细胞存活率超过95%。测量的每个iPSC因子的基因表达水平比以前使用单个小鼠胚胎成纤维细胞的研究报告的表达水平高10倍以上。我们的结果表明,使用HDEN转染质粒DNA生成iPSC可能是在不久的将来使用病毒转染方法的一种可行且安全的替代方法。

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