scholarly journals Efficient and Stable Transgene Expression in Human Embryonic Stem Cells Using Transposon-Mediated Gene Transfer

Stem Cells ◽  
2007 ◽  
Vol 25 (11) ◽  
pp. 2919-2927 ◽  
Author(s):  
Andrew Wilber ◽  
Jonathan L. Linehan ◽  
Xinghui Tian ◽  
Petter S. Woll ◽  
Julie K. Morris ◽  
...  
Stem Cells ◽  
2008 ◽  
Vol 26 (6) ◽  
pp. 1436-1443 ◽  
Author(s):  
Kristi A. Hohenstein ◽  
April D. Pyle ◽  
Jing Yi Chern ◽  
Leslie F. Lock ◽  
Peter J. Donovan

2010 ◽  
Vol 19 (4) ◽  
pp. 569-578 ◽  
Author(s):  
Cornelia M. Bertram ◽  
Susan M. Hawes ◽  
Simone Egli ◽  
Swee Lim Peh ◽  
Mirella Dottori ◽  
...  

Stem Cells ◽  
2007 ◽  
Vol 25 (4) ◽  
pp. 1055-1061 ◽  
Author(s):  
Jieming Zeng ◽  
Juan Du ◽  
Ying Zhao ◽  
Nallasivam Palanisamy ◽  
Shu Wang

2009 ◽  
Vol 12 (1) ◽  
pp. 15-24 ◽  
Author(s):  
Feng Cao ◽  
Xiaoyan Xie ◽  
Timothy Gollan ◽  
Li Zhao ◽  
Kazim Narsinh ◽  
...  

2010 ◽  
Vol 19 (6) ◽  
pp. 763-771 ◽  
Author(s):  
You-Tzung Chen ◽  
Kenryo Furushima ◽  
Pei-Shan Hou ◽  
Amy T. Ku ◽  
Jian Min Deng ◽  
...  

Stem Cells ◽  
2008 ◽  
Vol 26 (2) ◽  
pp. 525-533 ◽  
Author(s):  
Xiaofeng Xia ◽  
Melvin Ayala ◽  
Benjamin R. Thiede ◽  
Su-Chun Zhang

2011 ◽  
Vol 392 (10) ◽  
pp. 887-895 ◽  
Author(s):  
Melanie Wurm ◽  
Benjamin Groß ◽  
Malte Sgodda ◽  
Ludger Ständker ◽  
Thomas Müller ◽  
...  

AbstractGenetic modification of human embryonic stem cells (hESCs) using biophysical DNA transfection methods are hampered by the very low single cell survival rate and cloning efficiency of hESCs. Lentiviral gene transfer strategies are widely used to genetically modify hESCs but limited transduction efficiencies in the presence of feeder or stroma cells present problems, particularly if vesicular stomatitis virus glycoprotein (VSV-G) pseudotyped viral particles are applied. Here, we investigated whether the recently described semen derived enhancer of virus infection (SEVI) and alternative viral envelope proteins derived from either Gibbon ape leukaemia virus (GALV) or feline leukaemia virus (RD114) are applicable for transducing hESCs during co-culture with feeder or stroma cells. Our first set of experiments demonstrates that SEVI has no toxic effect on murine or hESCs and that exposure to SEVI does not interfere with the pluripotency-associated phenotype. Focusing on hESCs, we were able to further demonstrate that SEVI increases the transduction efficiencies of GALV and RD114 pseudotyped lentiviral vectors. More importantly, aiming at targeted differentiation of hESCs into functional somatic cell types, GALV pseudotyped lentiviral particles could efficiently and exclusively transduce hESCs grown in co-culture with OP9-GFP stroma cells (which were often used to induce differentiation into haematopoietic derivatives).


Stem Cells ◽  
2008 ◽  
Vol 26 (4) ◽  
pp. 1094-1094
Author(s):  
Chee-Gee Liew ◽  
Jonathan S. Draper ◽  
James Walsh ◽  
Harry Moore ◽  
Peter W. Andrews

Sign in / Sign up

Export Citation Format

Share Document