Li Shiwei, Xie Xiaoli, Yang Xiaodong, Liu Lijun, Tang Xueyang
Department of Pediatric Surgery, West China Hospital, Sichuan University, Chengdu Sichuan, 610041, P.R.China.
Department of Pediatric Surgery, Guangzhou Women and Children's Medical Center, Guangzhou Guangdong, 510623, P.R.China.
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2017 Apr 15;31(4):437-442. doi: 10.7507/1002-1892.201611059.
To investigate the effect of ultrasonic irradiation time on enhanced green fluorescent protein (EGFP) gene transfection efficiency and local tissue in bone defects using ultrasound-mediated microbubble destruction.
Thirty 3-month-old New Zealand rabbits (2.5-3.0 kg in weight) were randomly divided into 5 groups ( =6) and bone defect models were made on the right ulna. At 10 days after modeling, suspension of microbubbles and EGFP plasmids were locally injected (0.3 mL/kg) and then ultrasound was performed on defect at a frequency of 1 MHz, a intensity of 0.5 W/cm , and a duty ratio of 20% for 1, 2, 3, 4, and 5 minutes respectively (in 1, 2, 3, 4, and 5 minutes groups respectively). The survival condition was observed. Rabbits were sacrificed for gross observation at 7 days after transfer. The gene expression was observed by fluorescence staining. HE staining and transmission electron microscopy were used to observe the local tissue damage.
The animals all survived. New soft tissue formed in bone defects area at 1 week after transfer, the surrounding muscle tissue was partly filled in it. Green fluorescence expression was observed in all rabbits. The expression was the strongest in 2 minutes group, and was the weakest in 1 minute group. The absorbance ( ) value showed significant differences when compared 1 minute and 2 minutes groups with other groups ( <0.05), but no significant difference was found between 3, 4, and 5 minutes groups ( >0.05). Tissue damage was observed in all groups and it was aggravated with the increase of irradiation time.
EGFP transfection efficiency in bone defect by ultrasound-mediated microbubble destruction is related to irradiation time. EGFP gene can be efficiently transfected without obvious toxicity at 1 MHz, 0.5W/cm , and duty ratio of 20% for 2 minutes in bone defects of rabbits.
探讨超声辐照时间对超声介导微泡破坏增强绿色荧光蛋白(EGFP)基因转染效率及骨缺损局部组织的影响。
将30只3月龄新西兰兔(体重2.5 - 3.0 kg)随机分为5组(每组n = 6),于右侧尺骨制作骨缺损模型。造模后10天,局部注射微泡与EGFP质粒混悬液(0.3 mL/kg),然后分别以1 MHz频率、0.5 W/cm²强度、20%占空比,对缺损部位进行1、2、3、4、5分钟超声辐照(分别为1、2、3、4、5分钟组)。观察动物存活情况。转染后7天处死兔子进行大体观察。通过荧光染色观察基因表达情况。采用苏木精-伊红(HE)染色及透射电子显微镜观察局部组织损伤情况。
动物均存活。转染后1周骨缺损区有新的软组织形成,周围肌肉组织部分填充其中。所有兔子均观察到绿色荧光表达。2分钟组表达最强,1分钟组最弱。1分钟组和2分钟组与其他组比较吸光度(A)值差异有统计学意义(P < 0.05),但3、4、5分钟组之间差异无统计学意义(P > 0.05)。所有组均观察到组织损伤,且随辐照时间延长而加重。
超声介导微泡破坏在骨缺损中EGFP转染效率与辐照时间有关。在兔骨缺损中,以1 MHz频率、0.5W/cm²强度、20%占空比超声辐照2分钟可有效转染EGFP基因且无明显毒性。