| Literature DB >> 21285354 |
Núria Montserrat1, Elena Garreta, Federico González, Jordán Gutiérrez, Cristina Eguizábal, Víctor Ramos, Salvador Borrós, Juan Carlos Izpisua Belmonte.
Abstract
Reprogramming of somatic cells to induced pluripotent stem (iPS) cells can be achieved by the delivery of a combination of transcription factors, including Oct4, Sox2, Klf4, and c-Myc. Retroviral and lentiviral vectors are commonly used to express these four reprogramming factors separately and obtain reprogrammed iPS cells. Although efficient and reproducible, these approaches involve the time-consuming and labor-intensive production of retroviral or lentiviral particles together with a high risk of working with potentially harmful viruses overexpressing potent oncogenes, such as c-Myc. Here, we describe a simple method to produce bona fide iPS cells from human fibroblasts using poly-β-amino esters as the transfection reagent for the delivery of a single CAG-driven polycistronic plasmid expressing Oct4, Sox2, Klf4, c-Myc, and a GFP reporter gene (OSKMG). We demonstrate for the first time that poly-β-amino esters can be used to deliver a single polycistronic reprogramming vector into human fibroblasts, achieving significantly higher transfection efficiency than with conventional transfection reagents. After a protocol of serial transfections using poly-β-amino esters, we report a simple methodology to generate human iPS cells from human fibroblasts avoiding the use of viral vectors.Entities:
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Year: 2011 PMID: 21285354 PMCID: PMC3069445 DOI: 10.1074/jbc.M110.168013
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157