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Efficient Generation of Integration-Free Human Induced Pluripotent Stem Cells From Keratinocytes by Simple Transfection of Episomal Vectors

机译:通过游离载体的简单转染从角质形成细胞有效生成无整合的人类诱导多能干细胞。

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Keratinocytes represent an easily accessible cell source for derivation of human induced pluripotent stem (hiPS) cells, reportedly achieving higher reprogramming efficiency than fibroblasts. However, most studies utilized a retroviral or lentiviral method for reprogramming of keratinocytes, which introduces undesirable transgene integrations into the host genome. Moreover, current protocols of generating integration-free hiPS cells from keratinocytes are mostly inefficient. In this paper, we describe a more efficient, simple-to-use, and cost-effective method for generating integration-free hiPS cells from keratinocytes. Our improved method using lipid-mediated transfection achieved a reprogramming efficiency of [~]0.14% on average. Keratinocyte-derived hiPS cells showed no integration of episomal vectors, expressed stem cell-specific markers and possessed potentials to differentiate into all three germ layers by in vitro embryoid body formation as well as in vivo teratoma formation. To our knowledge, this represents the most efficient method to generate integration-free hiPS cells from keratinocytes.
机译:角质形成细胞代表了人类诱导的多能干(hiPS)细胞衍生的容易获得的细胞来源,据报道它比成纤维细胞具有更高的重编程效率。然而,大多数研究利用逆转录病毒或慢病毒方法对角质形成细胞进行重编程,这将不良的转基因整合引入宿主基因组。此外,目前从角质形成细胞生成无整合性hiPS细胞的协议大多效率低下。在本文中,我们描述了一种从角质形成细胞生成无整合性hiPS细胞的更有效,易用且经济高效的方法。我们使用脂质介导的转染方法的改良方法平均达到[〜] 0.14%的重编程效率。角质形成细胞衍生的hiPS细胞未整合游离型载体,表达干细胞特异性标记,并具有通过体外胚状体形成和体内畸胎瘤形成而分化为所有三个胚层的潜力。据我们所知,这是从角质形成细胞生成无整合性hiPS细胞的最有效方法。

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