Transfection is a gene delivery tool that is a popular means of manipulating cellular properties, such as induced pluripotent stem cell (iPSC) generation by reprogramming factors (Yamanaka factors). However, the efficiency of transfection needs to be improved. In the present study, three transfection protocols - non-liposomal transfection (NLT), magnetofection and electroporation - were compared by analysis of their transfection efficiencies and cell viabilities using human dental pulp cells (hDPC) and bovine fetal fibroblasts (bFF) as cell sources. Enhanced green fluorescent protein gene was used as the delivery indicator. For magnetofection, Polymag reagent was administrated. NLT, FuGENE-HD and X-treme GENE 9 DNA transfection reagents were used for NLT. For electroporation, the Neon(TM) and NEPA21(TM) electroporators were tested. Neon(TM) electroporation showed highest transfection efficiency when compared with NLT, magnetofection, and NEPA21(TM) electroporation, with transfection efficiency of about 33% in hDPC and 50% in bFF, based on viable cell population in each cell type. These results suggest that transfection by Neon(TM) electroporation can be used to deliver foreign genes efficiently in human and bovine somatic cells.
Cell Survival ; Cells, Cultured* ; Dental Pulp ; DNA ; Electroporation ; Fibroblasts ; Genes, vif ; Humans ; Indicators and Reagents ; Pluripotent Stem Cells ; Transfection*