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首页> 外文期刊>Japanese Journal of Ophthalmology >Induction of gene into the rabbit eye by iontophoresis: preliminary report.
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Induction of gene into the rabbit eye by iontophoresis: preliminary report.

机译:离子电渗疗法将基因导入兔眼:初步报告。

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PURPOSE: To assess the transfer of 6-carboxyfluorescein (6-FAM)-labeled phosphorothioate oligonucleotides(S-ODNs) into the ocular tissues, their stability, and possibility of injury to the ocular tissues. METHODS: The S-ODNs(2 mL/eye)were transduced noninvasively into albino rabbit eyes.The iontophoresis group consisted of 6 rabbits (12 eyes); the control group consisted of 2 rabbits (4 eyes) given eye drops containing S-ODNs. Aqueous humor and vitreous humor were collected after iontophoresis, subjected to electrophoresis with a fluorescence DNA sequencer and analyzed by the Gene Scan program. Frozen sections, 10-microm thick, were prepared for observation under a fluorescence microscope. A plasmid 4.7 kbp in size that expresses green fluorescent protein (GFP) was induced into the 18 eyes of 9 rabbits by the same procedure. RESULTS: In the iontophoresis group, S-ODNs were detected in the anterior chamber 5 minutes after electrophoresis began and in the vitreous after 10 minutes. These S-ODNs maintained the same length as at the initial synthesis. The S-ODNs could also be detected in the posterior retina 20 minutes after electrophoresis. No evidence of degeneration or inflammation due to the above procedure was found in the ocular tissues. Fluorescence showing GFP gene expression was found in the cornea, the anterior chamber angle, and the ciliary subepithelial tissues. CONCLUSIONS: These findings show that iontophoresis is an effective method to induce genes into the rabbit eye.
机译:目的:评估6-羧基荧光素(6-FAM)标记的硫代磷酸酯寡核苷酸(S-ODNs)向眼组织的转移,稳定性和对眼组织的伤害。方法:将S-ODNs(2 mL /眼)无创地转入白化病兔眼。离子电渗疗法组由6只兔(12只眼)组成。对照组由2只兔子(4只眼)组成,给予含有S-ODN的滴眼液。离子电渗疗法后收集房水和玻璃体液,用荧光DNA测序仪进行电泳,并通过基因扫描程序进行分析。准备10微米厚的冷冻切片,以便在荧光显微镜下观察。用相同的方法将大小为4.7kbp的表达绿色荧光蛋白(GFP)的质粒引入9只兔的18只眼中。结果:在离子电渗疗法组中,电泳开始后5分钟,在前房中检测到了S-ODN,而在10分钟后,在玻璃体中检测到了S-ODN。这些S-ODN保持与初始合成时相同的长度。电泳后20分钟,还可以在视网膜后部检测到S-ODN。在眼组织中未发现由于上述过程引起的变性或炎症的证据。在角膜,前房角和睫状上皮下组织中发现了显示GFP基因表达的荧光。结论:这些发现表明离子电渗疗法是一种将基因导入兔眼的有效方法。

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