Open AccessNucleofection Mediates High‐Efficiency Stable Gene Knockdown and Transgene Expression in Human Embryonic Stem Cells
Author(s) -
Hohenstein Kristi A.,
Pyle April D.,
Chern Jing Yi,
Lock Leslie F.,
Donovan Peter J.
Publication year - 2008
Publication title -
stem cells
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.159
H-Index - 229
eISSN - 1549-4918
pISSN - 1066-5099
DOI - 10.1634/stemcells.2007-0857
Subject(s) - nucleofection , biology , transfection , embryonic stem cell , stem cell , homeobox protein nanog , transgene , microbiology and biotechnology , induced pluripotent stem cell , electroporation , gene knockdown , gene delivery , transduction (biophysics) , cell culture , gene , genetics , biochemistry
High‐efficiency genetic modification of human embryonic stem (hES) cells would enable manipulation of gene activity, routine gene targeting, and development of new human disease models and treatments. Chemical transfection, nucleofection, and electroporation of hES cells result in low transfection efficiencies. Viral transduction is efficient but has significant drawbacks. Here we describe techniques to transiently and stably express transgenes in hES cells with high efficiency using a widely available vector system. The technique combines nucleofection of single hES cells with improved methods to select hES cells at clonal density. As validation, we reduced Oct4 and Nanog expression using siRNAs and shRNA vectors in hES cells. Furthermore, we derived many hES cell clones with either stably reduced alkaline phosphatase activity or stably overexpressed green fluorescent protein. These clones retained stem cell characteristics (normal karyotype, stem cell marker expression, self‐renewal, and pluripotency). These studies will accelerate efforts to interrogate gene function and define the parameters that control growth and differentiation of hES cells. Disclosure of potential conflicts of interest is found at the end of this article.