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Monitoring cell line identity in collections of human induced pluripotent stem cells - ScienceDirect

机译:监测人类诱导的多能干细胞集合中的细胞系同一性-ScienceDirect

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The ability to reprogram somatic cells into induced pluripotent stem cells (hiPSCs) has led to the generation of large collections of cell lines from thousands of individuals with specific phenotypes, many of which will be shared among different research groups as invaluable tools for biomedical research. As hiPSC-based research involves extensive culture of many cell lines, the issue periodic cell line identification is particularly important to ensure that cell line identity remains accurate. Here we analyzed the different commercially available genotyping methods considering ease of in-house genotyping, cost and informativeness, and applied one of them in our workflow for hiPSC generation. We show that the chosen STR method was able to establish a unique DNA profile for each of the 35 individuals/hiPSC lines at the examined sites, as well as identify two discrepancies resulting from inadvertently exchanged samples. Our results highlight the importance of hiPSC line genotyping by an in-house method that allows periodic cell line identification and demonstrate that STR is a useful approach to supplement less frequent karyotyping and epigenetic evaluations.
机译:将体细胞重编程为诱导性多能干细胞(hiPSC)的能力已导致从成千上万具特定表型的个体中产生大量细胞系,其中许多将在不同研究组之间共享,作为生物医学研究的宝贵工具。由于基于hiPSC的研究涉及许多细胞系的广泛培养,因此定期进行细胞系鉴定对于确保细胞系同一性保持准确至关重要。在这里,我们考虑了内部基因分型的简便性,成本和信息性,分析了各种可商购的基因分型方法,并将其中一种应用于我们的hiPSC生成工作流程。我们表明,所选的STR方法能够为所检查的站点上的35个个体/ hiPSC系中的每一个建立独特的DNA谱,以及识别由于无意间交换样品而导致的两个差异。我们的研究结果突出了通过内部方法进行hiPSC细胞系基因分型的重要性,该方法可以定期鉴定细胞系,并证明STR是补充频率较低的核型分析和表观遗传学评估的有用方法。

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