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从球形模板化纤维蛋白支架递送非病毒基因载体以实现持续的转基因表达。

Delivery of non-viral gene carriers from sphere-templated fibrin scaffolds for sustained transgene expression.

作者信息

Saul Justin M, Linnes Michael P, Ratner Buddy D, Giachelli Cecilia M, Pun Suzie H

机构信息

Department of Bioengineering, University of Washington, 1705 NE Pacific Street, W.H. Foege Building, Room N530P, Mailstop 355061, Seattle, WA 98195, USA.

出版信息

Biomaterials. 2007 Nov;28(31):4705-16. doi: 10.1016/j.biomaterials.2007.07.026. Epub 2007 Aug 6.

Abstract

Delivery of safe and controlled levels of biomimetic cues to govern host response and reorganization is a fundamental component in the design of tissue engineering scaffolds. Non-viral gene delivery is an approach that exploits the cell machinery to produce proteins while avoiding genomic DNA incorporation. We describe a method to integrate polymeric non-viral gene carriers (polyplexes) within a novel three-dimensional, sphere-templated fibrin scaffold suitable for soft tissue engineering applications. After seeding the scaffolds with NIH-3T3 fibroblasts, different transgene expression profiles were achieved based on the spatial distribution of polyplexes within the scaffold. Scaffolds with polyplexes coated onto the surface of inter-connected pores showed peak transfection at day 5 and linear expression through 15 days. Scaffolds with polyplexes embedded within the fibrils of the biopolymer showed peak expression at 7-9 days and showed linear expression for 21-29 days, depending on the polymer:DNA ratio. Surface-coated polyplexes achieved one order of magnitude greater expression than polyplexes embedded within the scaffold. The integrated material formulations developed in this work provide a useful technology for tissue engineering applications by demonstrating the ability to provide long-term biomimetic cues through non-viral gene delivery.

摘要

传递安全且可控水平的仿生信号以调控宿主反应和组织重塑是组织工程支架设计的基本要素。非病毒基因传递是一种利用细胞机制产生蛋白质同时避免基因组DNA整合的方法。我们描述了一种将聚合物非病毒基因载体(多聚体)整合到一种适用于软组织工程应用的新型三维、球形模板化纤维蛋白支架中的方法。在用NIH-3T3成纤维细胞接种支架后,基于支架内多聚体的空间分布实现了不同的转基因表达谱。多聚体包被在相互连通孔隙表面的支架在第5天显示出转染峰值,并在15天内呈线性表达。多聚体嵌入生物聚合物纤维内的支架在7 - 9天显示出表达峰值,并根据聚合物与DNA的比例在21 - 29天内呈线性表达。表面包被的多聚体比嵌入支架内的多聚体表达量高一个数量级。本研究中开发的集成材料配方通过展示通过非病毒基因传递提供长期仿生信号的能力,为组织工程应用提供了一项有用的技术。

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