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首页> 外文期刊>Gene therapy >In vivo gene transfer to the mouse eye using an HIV-based lentiviral vector; efficient long-term transduction of corneal endothelium and retinal pigment epithelium.
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In vivo gene transfer to the mouse eye using an HIV-based lentiviral vector; efficient long-term transduction of corneal endothelium and retinal pigment epithelium.

机译:使用基于HIV的慢病毒载体进行体内基因转移到小鼠眼;角膜内皮和视网膜色素上皮的长期有效转导。

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摘要

We have evaluated the transduction profiles of an HIV-based lentiviral vector delivered regionally to ocular tissues in vivo. Following subretinal injection, a green fluorescent protein (GFP) reporter gene was efficiently and stably expressed in retinal pigment epithelial (RPE) cells. Limited transduction of adjacent photoreceptors occurred in newborn mice, but was inefficient in adult animals. Injection of the vector into the anterior chamber resulted in efficient and stable transduction of corneal endothelial cells. Efficient in vivo gene transfer into cells of the corneal endothelium and retinal pigment epithelium by lentiviral vectors may therefore offer a valuable approach to the treatment of disorders of the cornea and outer retina.
机译:我们已经评估了基于艾滋病毒的慢病毒载体在体内局部递送至眼组织的转导概况。视网膜下注射后,绿色荧光蛋白(GFP)报告基因在视网膜色素上皮(RPE)细胞中有效稳定地表达。新生小鼠中邻近感光器的转导作用有限,但在成年动物中效率低下。载体注入前房导致角膜内皮细胞的有效和稳定的转导。因此,通过慢病毒载体将体内基因有效地转移到角膜内皮和视网膜色素上皮细胞中,可能为治疗角膜和视网膜外层疾病提供有价值的方法。

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