Comparison of ectopic gene expression methods in rat neural stem cells.

Authors:
Kim W, Kim JH, Kong SY, Park MH, Sohn UD, Kim HJ.
In:
Source: J Physiol
Publication Date: (2013)
Issue: 17(1): 23-30
Research Area:
Neurobiology
Cells used in publication:
Neural stem cell (NSC), rat
Species: rat
Tissue Origin: brain
Platform:
4D-Nucleofector® X-Unit
Experiment
Summary (by Lonza): The authors compared lipofection, electroporation, Nucleofection™ and retroviral transduction in order to identify the most efficient method to transfect rat neural stem cells (NSC). With about 35% transfection efficiency, the 4D-Nucleofector™ System outperformed lipofection (only 3-4%), standard electroporation using the Nepagene Nepa21 system (about 25%) and retroviral transduction (about 30%).
Abstract
Neural stem cells (NSCs) have the ability to proliferate and differentiate into various types of cells that compose the nervous system. To study functions of genes in stem cell biology, genes or siRNAs need to be transfected. However, it is difficult to transfect ectopic genes into NSCs. Thus to identify the suitable method to achieve high transfection efficiency, we compared lipid transfection, electroporation, nucleofection and retroviral transduction. Among the methods that we tested, we found that nucleofection and retroviral transduction showed significantly increased transfection efficiency. In addition, with retroviral transduction of Ngn2 that is known to induce neurogenesis in various types of cells, we observed facilitated final cell division in rat NSCs. These data suggest that nucleofection and retroviral transduction provide high efficiency of gene delivery system to study functions of genes in rat NSCs.