Wang Yu-Yan, Znou Zhong-Jiang, Zhang Xiang, Wu Sai-Zhu
Department of Cardiology, Nanfang Hospital, Department of Anatomy, Guangdong Provincial Key Laboratory of Tissue Construction and Inspection, Southern Medical University, Guangzhou 510515, China.
Nan Fang Yi Ke Da Xue Xue Bao. 2008 Jun;28(6):972-5.
To investigate the effect of therapeutic ultrasound on enhancing albumin microbubble-mediated gene delivery and evaluate the cytoskeletal damages in endothelial cells (ECs).
The ECs cultured in 6-well plates were transfected with the plasmid eGFP in the presence or absence of the microbubbles at different concentrations, followed by ultrasound exposure for 30 to 180 s at 2 MHz, with the mechanical index (MI) of 0.5-1.8. The gene transfection efficiency was evaluated by observing the green fluorescence of the cells, and the cytoskeletal damage was assessed using immunofluorescence staining 24 to 48 h after ultrasound exposure.
Within the MI range of ultrasound exposure between 0.50 and 1.00, the gene transfection efficiency was positively correlated to MI (P<0.001), and further increment of the MI failed to further increase the transfection efficiency. The duration of ultrasound exposure, within the range of 30-90 s, was also positively correlated to the gene transfection efficiency and microtubule fluorescence intensity(P<0.001), and prolonged exposure did not further enhance the effects. Variation of the MI and ultrasound exposure time within the above ranges did not cause significant changes in the florescence intensity of the microfilaments (P>0.05).
Albumin microbubbles in the presence of ultrasound exposure can substantially enhance the gene transfection efficiency due to therapeutic ultrasound-mediated microbubble destruction without causing obvious damage of the cytoskeletons, and allows safe and efficient nonviral gene delivery in gene therapy.
研究治疗性超声对增强白蛋白微泡介导的基因递送的作用,并评估其对内皮细胞(ECs)细胞骨架的损伤。
将培养在6孔板中的ECs在有或无不同浓度微泡的情况下用质粒eGFP转染,随后以2MHz超声暴露30至180秒,机械指数(MI)为0.5 - 1.8。通过观察细胞的绿色荧光评估基因转染效率,并在超声暴露后24至48小时使用免疫荧光染色评估细胞骨架损伤。
在超声暴露的MI范围为0.50至1.00时,基因转染效率与MI呈正相关(P<0.001),MI进一步增加未能进一步提高转染效率。超声暴露持续时间在30 - 90秒范围内,也与基因转染效率和微管荧光强度呈正相关(P<0.001),延长暴露时间并未进一步增强效果。在上述范围内MI和超声暴露时间的变化未引起微丝荧光强度的显著变化(P>0.05)。
在超声暴露下白蛋白微泡可通过治疗性超声介导的微泡破坏显著提高基因转染效率,且不会引起细胞骨架的明显损伤,从而在基因治疗中实现安全有效的非病毒基因递送。