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明胶纳米粒作为基因载体在转基因鸡中的应用。

Gelatin nanoparticles as gene carriers for transgenic chicken applications.

机构信息

Division of Medical Engineering Research, National Health Research Institutes, Zhunan Town, Miaoli County 350, Taiwan, ROC.

出版信息

J Biomater Appl. 2013 May;27(8):1055-65. doi: 10.1177/0885328211434089. Epub 2012 Jan 19.

Abstract

To develop a safe and effective nonviral gene delivery system for transgenic chicken manipulation, we developed gelatin nanocarriers using a reporter plasmid (pEGFP-C1; enhanced green fluorescence protein, EGFP) that expressed EGFP. pEGFP-C1-containing gelatin nanoparticles (GP/pEGFP) were prepared using a water-ethanol solvent displacement method and characterized by size, surface charge, DNA loading, and DNA protection ability. For gene delivery, pEGFP-C1 was stably and efficiently encapsulated in GPs that were approximately 300 nm in diameter with a slight negative surface charge, which was prepared from gelatin solution at pH 8.0. Approximately, 85% of the plasmid DNA was encapsulated in the GPs. Electrophoresis results showed that the GPs provided protection against DNase I digestion. We used the GP/pEGFP as a vector to transfect cells and chicken embryos. The vector was nontoxic to cells, and GFP expression was effectively expressed 24 h after HeLa cell transfection. Direct injection was adapted for vector transport to the chicken embryo; injection in the area opaca (Ao) of the egg resulted in the highest hatching rate without affecting embryo development. GFP gene expression in embryo sections was observed 4 days after injection. The results of this study demonstrate that GPs are a suitable nonviral vector for delivering exogenous genes for transgenic chicken manipulation.

摘要

为了开发用于转基因鸡操作的安全有效的非病毒基因传递系统,我们使用表达 EGFP 的报告质粒(pEGFP-C1;增强型绿色荧光蛋白,EGFP)开发了明胶纳米载体。使用水-乙醇溶剂置换法制备含 pEGFP-C1 的明胶纳米颗粒(GP/pEGFP),并通过粒径、表面电荷、DNA 负载和 DNA 保护能力进行表征。用于基因传递,pEGFP-C1 稳定且高效地封装在直径约 300nm 且带有轻微负表面电荷的 GP 中,该 GP 是由 pH 8.0 的明胶溶液制备的。大约 85%的质粒 DNA 被封装在 GP 中。电泳结果表明,GP 提供了对 DNase I 消化的保护。我们使用 GP/pEGFP 作为载体转染细胞和鸡胚。该载体对细胞无毒,在 HeLa 细胞转染 24 小时后有效表达 GFP。直接注射被用于载体向鸡胚的运输;在鸡蛋的暗区(Ao)注射导致孵化率最高,而不影响胚胎发育。注射后 4 天观察到胚胎切片中的 GFP 基因表达。这项研究的结果表明,GP 是用于转基因鸡操作的外源基因传递的合适非病毒载体。

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