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Electroporation and ultrasound enhanced non-viral gene delivery in vitro and in vivo

机译:电穿孔和超声增强体外和体内非病毒基因的递送

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Non-viral vectors are less efficient than the use of viral vectors for delivery of genetic material to cells in vitro and especially in vivo. However, viral vectors involve the use of foreign proteins that can stimulate both the innate and acquired immune response. In contrast, plasmid DNA can be delivered without carrier proteins and is non-immunogenic. Plasmid gene delivery can be enhanced by the use of physical methods that aid the passage of the plasmid through the cell membrane. Electroporation and microbubble-enhanced ultrasound are two of the most effective physical delivery methods and these can be applied to a range of different cell types in vitro and a broad range of tissues in vivo. Both techniques also have the advantage that, unlike viral vectors, they can be used to target specific tissues with systemic delivery. Although electroporation is often the more efficient of the two, microbubble-enhanced ultrasound causes less damage and is less invasive. This review provides an introduction to the methodology and summarises the range of cells and tissues that have been genetically modified using these techniques. Keywords Plasmid DNA - Physical methods - Gene transfer - Gene therapy - Microbubbles - Skeletal muscle
机译:非病毒载体的效率低于使用病毒载体将遗传物质体外,尤其是体内递送至细胞的效率。但是,病毒载体涉及使用外源蛋白质,该蛋白质可以刺激先天和后天免疫应答。相反,质粒DNA可以不带载体蛋白而被递送并且是非免疫原性的。可以通过使用有助于质粒通过细胞膜的物理方法来增强质粒基因的递送。电穿孔和微泡增强超声是最有效的两种物理递送方法,可以在体外应用于多种不同的细胞类型,在体内可以应用于多种组织。两种技术还具有的优点是,与病毒载体不同,它们可用于通过全身递送靶向特定组织。尽管电穿孔通常是两者中效率最高的一种,但微泡增强型超声造成的损伤较小且侵入性较小。这篇综述提供了该方法的简介,并总结了使用这些技术进行了基因修饰的细胞和组织的范围。质粒DNA-物理方法-基因转移-基因治疗-微泡-骨骼肌

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