| Literature DB >> 26237226 |
Daniel Paull1, Ana Sevilla1, Hongyan Zhou1, Aana Kim Hahn1, Hesed Kim1, Christopher Napolitano1, Alexander Tsankov2,3,4, Linshan Shang1, Katie Krumholz1, Premlatha Jagadeesan1, Chris M Woodard1, Bruce Sun1, Thierry Vilboux5,6, Matthew Zimmer1, Eliana Forero1, Dorota N Moroziewicz1, Hector Martinez1, May Christine V Malicdan5, Keren A Weiss1, Lauren B Vensand1, Carmen R Dusenberry1, Hannah Polus1, Karla Therese L Sy1, David J Kahler1, William A Gahl5,7, Susan L Solomon1, Stephen Chang1, Alexander Meissner2,3,4, Kevin Eggan2,3,4,8, Scott A Noggle1.
Abstract
Induced pluripotent stem cells (iPSCs) are an essential tool for modeling how causal genetic variants impact cellular function in disease, as well as an emerging source of tissue for regenerative medicine. The preparation of somatic cells, their reprogramming and the subsequent verification of iPSC pluripotency are laborious, manual processes limiting the scale and reproducibility of this technology. Here we describe a modular, robotic platform for iPSC reprogramming enabling automated, high-throughput conversion of skin biopsies into iPSCs and differentiated cells with minimal manual intervention. We demonstrate that automated reprogramming and the pooled selection of polyclonal pluripotent cells results in high-quality, stable iPSCs. These lines display less line-to-line variation than either manually produced lines or lines produced through automation followed by single-colony subcloning. The robotic platform we describe will enable the application of iPSCs to population-scale biomedical problems including the study of complex genetic diseases and the development of personalized medicines.Entities:
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Year: 2015 PMID: 26237226 DOI: 10.1038/nmeth.3507
Source DB: PubMed Journal: Nat Methods ISSN: 1548-7091 Impact factor: 28.547