A comparison of non-integrating reprogramming methods

Human induced pluripotent stem cells (hiPSCs) are useful in disease modeling and drug discovery, and they promise to provide a new generation of cell-based therapeutics. To date there has been no systematic evaluation of the most widely used techniques for generating integration-free hiPSCs. Here we...

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Published inNature biotechnology Vol. 33; no. 1; pp. 58 - 63
Main Authors Schlaeger, Thorsten M, Daheron, Laurence, Brickler, Thomas R, Entwisle, Samuel, Chan, Karrie, Cianci, Amelia, DeVine, Alexander, Ettenger, Andrew, Fitzgerald, Kelly, Godfrey, Michelle, Gupta, Dipti, McPherson, Jade, Malwadkar, Prerana, Gupta, Manav, Bell, Blair, Doi, Akiko, Jung, Namyoung, Li, Xin, Lynes, Maureen S, Brookes, Emily, Cherry, Anne B C, Demirbas, Didem, Tsankov, Alexander M, Zon, Leonard I, Rubin, Lee L, Feinberg, Andrew P, Meissner, Alexander, Cowan, Chad A, Daley, George Q
Format Journal Article
LanguageEnglish
Published United States Nature Publishing Group 01.01.2015
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Summary:Human induced pluripotent stem cells (hiPSCs) are useful in disease modeling and drug discovery, and they promise to provide a new generation of cell-based therapeutics. To date there has been no systematic evaluation of the most widely used techniques for generating integration-free hiPSCs. Here we compare Sendai-viral (SeV), episomal (Epi) and mRNA transfection mRNA methods using a number of criteria. All methods generated high-quality hiPSCs, but significant differences existed in aneuploidy rates, reprogramming efficiency, reliability and workload. We discuss the advantages and shortcomings of each approach, and present and review the results of a survey of a large number of human reprogramming laboratories on their independent experiences and preferences. Our analysis provides a valuable resource to inform the use of specific reprogramming methods for different laboratories and different applications, including clinical translation.
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ISSN:1087-0156
1546-1696
1546-1696
DOI:10.1038/nbt.3070