[Comparison of different methods of pEGFP-actin plasmid transfection to the endothelium].
Qin Luo, Jie Qi, Jian Chen, Xiangdong Luo, Zongcheng Yang
Abstract
Qin Luo, Jie Qi, Jian Chen, Xiangdong Luo, Zongcheng Yang
Abstract
OBJECTIVE: To screen the optimal transfection method for human umbilical vein endothelium, so as for us to establish a basic method for the further transfection with other objective genes. METHODS: The pEGFP-Actin plasmid was employed as an ectogenetic gene and was transfected into ECV-304 endothelium cells by lipofection, DEAE-dextran or electroporation transfection methods, respectively. The cell death rate and transfection rate after the transfection were compared among the three methods. RESULTS: (1) Twelve hours after the transfection, the cell death rate was 4% by all three methods, however, the cell death rate increased up to 50% at 60 hours after the transfection by DEAE-dextran. (2) The transfection rate of ECV-304 could reach 95% by all the three methods. But the fluorescent intensity was stronger in lipofection group compared with electroporation method. CONCLUSION: Gene transfection into ECV-304 with lipofection and electroporation methods exhibited better stability and repeatability.
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OBJECTIVE: To screen the optimal transfection method for human umbilical vein endothelium, so as for us to establish a basic method for the further transfection with other objective genes. METHODS: The pEGFP-Actin plasmid was employed as an ectogenetic gene and was transfected into ECV-304 endothelium cells by lipofection, DEAE-dextran or electroporation transfection methods, respectively. The cell death rate and transfection rate after the transfection were compared among the three methods. RESULTS: (1) Twelve hours after the transfection, the cell death rate was 4% by all three methods, however, the cell death rate increased up to 50% at 60 hours after the transfection by DEAE-dextran. (2) The transfection rate of ECV-304 could reach 95% by all the three methods. But the fluorescent intensity was stronger in lipofection group compared with electroporation method. CONCLUSION: Gene transfection into ECV-304 with lipofection and electroporation methods exhibited better stability and repeatability.
Key concepts: Transfection, Electroporation, Molecular biology, Genetic enhancement, Biology, Cell, Umbilical vein, Cell culture