| Literature DB >> 25437882 |
Thorsten M Schlaeger1, Laurence Daheron2, Thomas R Brickler2, Samuel Entwisle2, Karrie Chan3, Amelia Cianci3, Alexander DeVine3, Andrew Ettenger3, Kelly Fitzgerald3, Michelle Godfrey3, Dipti Gupta3, Jade McPherson3, Prerana Malwadkar3, Manav Gupta3, Blair Bell3, Akiko Doi4, Namyoung Jung5, Xin Li5, Maureen S Lynes2, Emily Brookes3, Anne B C Cherry6, Didem Demirbas7, Alexander M Tsankov8, Leonard I Zon1, Lee L Rubin9, Andrew P Feinberg5, Alexander Meissner8, Chad A Cowan10, George Q Daley11.
Abstract
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.Entities:
Mesh:
Year: 2014 PMID: 25437882 PMCID: PMC4329913 DOI: 10.1038/nbt.3070
Source DB: PubMed Journal: Nat Biotechnol ISSN: 1087-0156 Impact factor: 54.908