摘要
背景:壳聚糖对软骨细胞具有良好的生物相容性和可降解性,但存在基因转染效率偏低的缺陷。目的:构建负载增强型绿色荧光蛋白基因的聚乙烯亚胺-壳聚糖/DNA纳米粒,检测其理化性能,以及体外对关节软骨细胞的基因转染效率。方法:将聚乙烯亚胺共价连接于壳聚糖骨架上构建聚乙烯亚胺-壳聚糖复合物,再将聚乙烯亚胺-壳聚糖与负载增强型绿色荧光蛋白基因的质粒DNA以复凝聚法制成纳米粒,以扫描电镜检测纳米粒形态,Zeta电位粒度分析仪测定其粒径、表面电位;凝胶电泳阻滞实验观察聚乙烯亚胺-壳聚糖和质粒DNA的结合力。以聚乙烯亚胺-壳聚糖/DNA纳米粒、裸质粒DNA、脂质体2000及壳聚糖/DNA纳米粒转染体外培养的兔关节软骨细胞,流式细胞仪及荧光显微镜检测基因转染率;激光共聚焦显微镜检测DNA的入核情况。结果与结论:聚乙烯亚胺-壳聚糖/DNA纳米粒多呈球形,粒径为(154.6±18.6)nm,表面Zeta电位为(24.68±6.82)mV,可有效保护质粒DNA免受DNaseⅠ的降解。体外转染实验证明聚乙烯亚胺-壳聚糖/DNA纳米粒能介导增强型绿色荧光蛋白基因转染关节软骨细胞并在细胞内表达绿色荧光蛋白,转染率达(23.80±1.74)%,转染率高于裸质粒DNA组及壳聚糖/DNA纳米粒组(P<0.05),与脂质体2000组无显著差别(P=0.522)。表明聚乙烯亚胺-壳聚糖/DNA纳米粒能有效保护质粒DNA免受核酸酶降解,对关节软骨细胞有良好的基因转染能力。
BACKGROUND： Chitosan is well known as good biocompatibility and biodegradability; however, its extensive use in biomedical applications is restricted due to its poor transfection efficiency.OBJECTIVE： To prepare the polyethyleneimine-chitosan/DNA nanoparticles loading enhanced green fluorescent protein gene, and to detect their physicochemical properties and gene transfection efficiency towards chondrocytes in vitro.METHODS： Low molecular weight polyethyleneimine was covalently linked to chitosan backbone to construct chitosan-graft-polyethyleneimine; then the chitosan-graft-polyethyleneimine was mixed with DNA nanoparticles,which loaded enhanced green fluorescent protein gene, by a complex coacervation method. The nanoparticle morphology was observed under a scanning electron microscopy. The sizes and zeta-potentials of the nanoparticles were measured by a Marven-nano laser diffractometer. The binding capacity of plasmid DNA was evaluated by agarose gel electrophoresis analysis. The gene transfection experiments in vitro were performed towards rabbit＇s chondrocytes. The gene transfection efficiency was measured with flow cytometry and under fluorescence microscope. How marked DNA entered into the nucleus of chondrocytes mediated by thenanoparticles was detected by laser scanning confocal microscopy.RESULTS AND CONCLUSION： The prepared nanoparticles were mainly spherical, with an average size of（154.6±18.6） nm, and zeta-potential of（24.68±6.82） mV. The agarose gel electrophoresis analysis confirmed that the nanoparticles could effectively protect plasmid DNA from DNase Ⅰ-induced degradation. Gene transfection in vitro proved that the nanoparticles were efficient in transfecting rabbit＇s chondrocytes and the expression of green fluorescent proteins was observed under fluorescent microscope, with a transfection efficiency of（23.80±1.74）% that was significantly higher than that of the naked plasmid DNA and chitosan/DNA nanoparticles（P 0.05）. But no significant differences were observ
出处
《中国组织工程研究》
CAS
CSCD
2013年第47期8162-8168,共7页
Chinese Journal of Tissue Engineering Research
基金
国家自然科学基金资助项目(82172040
30600632)
广东省科技计划基金资助项目(2012B031800451)
广东省自然科学基金资助项目(S2011010004808)~~
