首页> 美国卫生研究院文献>Bosnian Journal of Basic Medical Sciences >COMPARATIVE ANALYSIS OF GENE TRANSFER TO HUMAN AND RAT RETINAL PIGMENT EPITHELIUM CELL LINE BY A COMBINATORIA! USE OF RECOMBINANT ADENO-ASSOCIATED VIRUS AND ULTRASOUND OR/AND MICROBUBBLES
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COMPARATIVE ANALYSIS OF GENE TRANSFER TO HUMAN AND RAT RETINAL PIGMENT EPITHELIUM CELL LINE BY A COMBINATORIA! USE OF RECOMBINANT ADENO-ASSOCIATED VIRUS AND ULTRASOUND OR/AND MICROBUBBLES

机译:组合法将基因转移到人和大鼠视网膜色素上皮细胞系的比较分析!重组腺伴随病毒和超声或/和微泡的使用

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摘要

Ultrasound-targeted microbubble destruction has been utilized to deliver a drug/gene into cells in both in vitro and in vivo studies. This work was performed to investigate the feasibility of gene transfer to human retinal pigment epithelium cell line(ARPE-19) and rat retinal pigment epithelium cell line(RPE-J) by a combinatorial use of recombinant adeno-associated virus (rAAV) and ultrasound (US) or/and mi-crobubbles (MBs) and compare the difference between them. Different doses of serotype 2 rAAV encoding a enhanced green fluorescent protein (rAAV2-EGFP) gene and MBs was administered to ARPE-19 and RPE-J cells under different US conditions. Transfection efficiency and cell viability were assessed by fluorescence microscopy, flow cytometry (FCM) analysis, trypan blue staining. The results indicated that US and MBs could respectively improve rAAV2mediated gene transfer to RPE-J cells, but neither US nor MBs could do so in ARPE- 19 cells. US plus MBs could significantly enhance rAAV2-mediated gene transfer to ARPE-19 cells, however, the same effects were not seen in RPE-J cells. These findings demonstrated it is not always coincident that US, MBs and US plus MBs exert the similar effects on gene transfer in vitro RPE cells. So, it is necessary to choose appropriate RPE cell line for the study of US or/and MBs-mediated rAAV gene transfer in retinal gene therapy.
机译:在体外和体内研究中,已将超声靶向微泡破坏用于将药物/基因递送到细胞中。通过重组腺相关病毒(rAAV)和超声的组合使用,研究了将基因转移到人视网膜色素上皮细胞系(ARPE-19)和大鼠视网膜色素上皮细胞系(RPE-J)的可行性。 (US)或/和微型垃圾(MB),并比较它们之间的差异。在不同的美国条件下,将不同剂量的编码增强型绿色荧光蛋白(rAAV2-EGFP)基因和MBs的血清型2 rAAV施用给ARPE-19和RPE-J细胞。通过荧光显微镜,流式细胞术(FCM)分析,锥虫蓝染色评估转染效率和细胞活力。结果表明,US和MBs可以分别改善rAAV2介导的基因向RPE-J细胞的转移,但是US和MBs在ARPE-19细胞中均不能。 US加MBs可以显着增强rAAV2介导的基因向ARPE-19细胞的转移,但是在RPE-J细胞中未观察到相同的作用。这些发现表明,US,MBs和US加MBs在体外RPE细胞的基因转移中发挥相似的作用并不总是一致的。因此,有必要选择合适的RPE细胞系来研究视网膜基因治疗中US或/和MBs介导的rAAV基因转移。

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