TY - JOUR
T1 - Simple generation of human induced pluripotent stem cells using poly-β-amino esters as the non-viral gene delivery system
AU - Montserrat, Núria
AU - Garreta, Elena
AU - González, Federico
AU - Gutiérrez, Jordán
AU - Eguizábal, Cristina
AU - Ramos, Víctor
AU - Borrós, Salvador
AU - Belmonte, Juan Carlos Izpisua
N1 - ©2011 by The American Society for Biochemistry and Molecular Biology, Inc.
PY - 2011/4/8
Y1 - 2011/4/8
N2 - 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.
AB - 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.
KW - Somatic-cells
KW - Fibroblasts
KW - Mouse
KW - Library
KW - Adult
KW - Expression
KW - Induction
UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=pure_univeritat_ramon_llull&SrcAuth=WosAPI&KeyUT=WOS:000289077500056&DestLinkType=FullRecord&DestApp=WOS
UR - https://www.scopus.com/record/display.uri?eid=2-s2.0-79953316849&origin=inward
U2 - 10.1074/jbc.M110.168013
DO - 10.1074/jbc.M110.168013
M3 - Article
C2 - 21285354
AN - SCOPUS:79953316849
SN - 0021-9258
VL - 286
SP - 12417
EP - 12428
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 14
ER -