电穿孔
脐静脉
生物
转染
细胞生物学
人脐静脉内皮细胞
分子生物学
脂质体
细胞培养
内皮干细胞
基因
体外
遗传学
载体(分子生物学)
重组DNA
作者
Julien Yockell‐Lelièvre,Valérie Riendeau,Steve Gagnon,Christophe Garenc,Marie Audette
标识
DOI:10.1089/dna.2009.0915
摘要
Primary endothelial cells are largely recognized as hard-to-transfect cells. We have been using a double-pulse electroporation technique to efficiently insert genetic material into human umbilical vein endothelial cell (HUVEC). Previously, this technique has been successfully used on hard-to-transfect monocytic cells. Using a conventional electroporation device, we have tested this protocol on HUVECs and compared it with conventional transfection techniques. The average transfection efficiency was up to 68% as measured by the ability of the cells to efficiently express the red fluorophore of the tdTomato gene. Similar results were obtained in human aortic endothelial cells and human microvascular endothelial cells. This technique does not require any particular expensive device, specific medium, or reagent, and the results we obtained so far exceed those of any other previous protocol. This is therefore an affordable and efficient transfection technique that opens new avenues in vascular endothelial research.
科研通智能强力驱动
Strongly Powered by AbleSci AI