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[1型和2型重组腺相关病毒转导大鼠脑内增强型绿色荧光蛋白的表达]

[Expression of enhanced green fluorescent protein in rat brain transduced by recombinant adeno-associated viruses type 1 and type 2].

作者信息

Li Shi-fang, Wang Ren-zhi, Li Gui-lin, Hu Guo-ji, Zhang Bo, Dou Wan-chen, Gu Jian-gang, Zhang Zhen-xing, Kong Yan-guo, Wei Jun-ji, Wei Yu-kui, Tian Yu

机构信息

Department of Neurosurgery, Peking Union Medical College Hospital, Peking Union Medical College, Beijing 100730, China.

出版信息

Zhonghua Yi Xue Za Zhi. 2005 Mar 2;85(8):542-6.

Abstract

OBJECTIVE

To explore the expression of enhanced green fluorescent protein (EGFP) transduced into the brain via recombinant adeno-associated virus (rAAV) type 1 and rAAV type 2 vectors so as to select the better rAAV serotype and feasible gene transfer route to central nervous system (CNS).

METHODS

Twenty-four SD male adult rats were randomly divided into 4 equal groups: rAAV1 intra-hippocampus injection group, rAAV1 intra-ventricular injection group, rAAV2 intra-hippocampus injection group, and rAAV2 intra-ventricular injection group to be injected stereotactically with titer and volume matched rAAV1-EGFP and rAAV2-EGFP vectors respectively. The rats were sacrificed respectively 2 and 4 weeks after injection and their brains were removed to be made into serial frozen coronal sections. Fluorescence microscopy was used to observe the expression of EGFP in the brain and to calculate the expression volume of EGFP in different parts of the brain.

RESULTS

Two weeks after injection EGFP was expressed in a small amount or not expressed in all groups. Four weeks after injection the EGFP expression volume were (7.00 +/- 0.98) mm(3) and (0.81 +/- 0.28) mm(3) in the rAAV1 and rAAV2 intra-hippocampus injection groups respectively (P < 0.01), and were (12.72 +/- 0.28) mm(3) and (0.24 +/- 0.13) mm(3) in the rAAV1 and rAAV2 intra-ventricular injection groups respectively (P < 0.001).

CONCLUSION

As gene-transducing vector in CNS rAAV1 is superior to rAAV2. High expression can be achieved by intra-ventricular injection with rAAV1 vectors.

摘要

目的

探讨通过重组1型腺相关病毒(rAAV)和2型腺相关病毒(rAAV)载体转导入脑内的增强型绿色荧光蛋白(EGFP)的表达情况,以筛选出更优的rAAV血清型及可行的中枢神经系统(CNS)基因转移途径。

方法

将24只成年雄性SD大鼠随机分为4组,每组6只:rAAV1海马注射组、rAAV1脑室内注射组、rAAV2海马注射组和rAAV2脑室内注射组,分别经立体定向注射滴度和体积匹配的rAAV1-EGFP和rAAV2-EGFP载体。注射后2周和4周分别处死大鼠,取脑制作连续冠状冰冻切片。采用荧光显微镜观察脑内EGFP的表达情况,并计算脑不同部位EGFP的表达量。

结果

注射后2周,各组EGFP均少量表达或未表达。注射后4周,rAAV1和rAAV2海马注射组EGFP表达量分别为(7.00±0.98)mm³和(0.81±0.28)mm³(P<0.01);rAAV1和rAAV2脑室内注射组EGFP表达量分别为(12.72±0.28)mm³和(0.24±0.13)mm³(P<0.001)。

结论

作为CNS基因转导载体,rAAV1优于rAAV2。rAAV1载体经脑室内注射可实现高效表达。

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