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-beta-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-beta-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-beta-amino esters, we report a simple methodology to generate human iPS cells from human fibroblasts avoiding the use of viral vectors.
| Original language | English |
|---|---|
| Pages (from-to) | 12417-12428 |
| Number of pages | 12 |
| Journal | Journal of Biological Chemistry |
| Volume | 286 |
| Issue number | 14 |
| DOIs | |
| Publication status | Published - 8 Apr 2011 |
Keywords
- Somatic-cells
- Fibroblasts
- Mouse
- Library
- Adult
- Expression
- Induction
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