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质粒大小影响壳聚糖纳米颗粒介导的基因向软骨细胞的转移。

Plasmid size influences chitosan nanoparticle mediated gene transfer to chondrocytes.

作者信息

Xu Ximing, Capito Ramille M, Spector Myron

机构信息

Tissue Engineering, VA Boston Healthcare System, Boston, Massachusetts 02130, USA.

出版信息

J Biomed Mater Res A. 2008 Mar 15;84(4):1038-48. doi: 10.1002/jbm.a.31479.

Abstract

The objective of the present study was to prepare chitosan nanoparticles incorporating a relatively large plasmid encoding for osteogenic protein (OP)-1 and to determine the ability of these nanoparticles to transfect adult canine articular chondrocytes in vitro. The positive charge of chitosan acted to condense the relatively large negatively-charged OP-1 plasmid such that it could be incorporated into nanoparticles. Incorporation of the plasmid into the chitosan nanoparticles did not affect the structural integrity of the plasmid as demonstrated by gel electrophoresis. The morphology and size of the nanoparticles were found to vary with the chitosan:plasmid weight ratio. Nanoparticles formulated with a chitosan:plasmid ratio of 10:1 were of uniformly small size (less than 250 nm) and spherical shape. These nanoparticles had a positive charge of about 20 mV. FITC-labeled chitosan nanoparticles were found in virtually all of the cells after 24 h of incubation with the nanoparticles, and confocal microscopy revealed FITC-related fluorescence in the nucleus of the chondrocytes. Although transfection of the chondrocytes was demonstrated by the fluorescence of cells treated with chitosan nanoparticles containing the plasmid for the enhanced green fluorescence protein, cells transfected with nanoparticles incorporating the larger OP-1 plasmid did not show OP-1 expression measured by ELISA for up to 2 weeks in culture. These results indicate that although a large plasmid can be successfully incorporated within chitosan nanoparticles, the size of the plasmid incorporated within the nanoparticles may still significantly affect gene transfer to cells.

摘要

本研究的目的是制备负载相对较大的编码成骨蛋白(OP)-1的质粒的壳聚糖纳米颗粒,并确定这些纳米颗粒在体外转染成年犬关节软骨细胞的能力。壳聚糖的正电荷作用于凝聚相对较大的带负电荷的OP-1质粒,使其能够被包入纳米颗粒中。如凝胶电泳所示,将质粒包入壳聚糖纳米颗粒中不会影响质粒的结构完整性。发现纳米颗粒的形态和大小随壳聚糖与质粒的重量比而变化。壳聚糖与质粒比例为10:1配制的纳米颗粒尺寸均匀较小(小于250 nm)且呈球形。这些纳米颗粒带约20 mV的正电荷。在用纳米颗粒孵育24小时后,几乎在所有细胞中都发现了异硫氰酸荧光素(FITC)标记的壳聚糖纳米颗粒,共聚焦显微镜显示软骨细胞核中有与FITC相关的荧光。尽管用含有增强型绿色荧光蛋白质粒的壳聚糖纳米颗粒处理的细胞的荧光证明了软骨细胞的转染,但在培养长达2周的时间内,用包入较大OP-1质粒的纳米颗粒转染的细胞通过酶联免疫吸附测定(ELISA)未显示OP-1表达。这些结果表明,尽管大质粒可以成功地包入壳聚糖纳米颗粒中,但包入纳米颗粒中的质粒大小仍可能显著影响基因向细胞的转移。

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