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用于靶向基因递送的谷胱甘肽响应性多层包覆金纳米颗粒

Glutathione-Responsive Multilayer Coated Gold Nanoparticles for Targeted Gene Delivery.

作者信息

Yu Feifei, Huang Jingbin, Yu Yuan, Lu Ying, Chen Yan, Zhang He, Zhou Guichen, Sun Zhiguo, Liu Junjie, Sun Duxin, Zhang Guoqing, Zou Hao, Zhong Yanqiang

出版信息

J Biomed Nanotechnol. 2016 Mar;12(3):503-15. doi: 10.1166/jbn.2016.2177.

DOI:10.1166/jbn.2016.2177
PMID:27280248
Abstract

Efficient gene release after intracellular uptake is very important for non-viral gene delivery systems. To construct a glutathione-responsive gene delivery system, we developed gold-cysteamine (AuCM)/plasmid DNA (pDNA)/poly TAT (pTAT)/hyaluronic acid (HA) nanocomplexes (AuCM/pDNA/pTAT/HA) in this study. The AuCM/pDNA/pTAT/HA nanocomplexes possessed a small size less than 200 nm and negative zeta potential of -17 ± 4 mV. The multilayer structure was verified by UV-Vis spectra, surface charges, dynamic light scattering. Morphology was observed by transmission electron microscope. The AuCM/pDNA/pTAT/HA nanocomplexes could completely protect pDNA against enzymatic degradation. These nanocomplexes showed effective cellular uptake in CD44 receptors over-expressed HepG 2 cells in a HA/CD44 interaction dependent manner. Moreover, transfection efficacy was significantly enhanced in AuCM/pDNA/pTAT/HA treated HepG 2 cells compared with AuCM/pDNA/pTAT, and was further enhanced in the presence of GSH, indicating that AuCM/pDNA/pTAT/HA was glutathione-responsive. Biodistribution revealed that AuCM/pDNA/pTAT/HA nanocomplexes mainly accumulated in liver. In conclusion, AuCM/pDNA/pTAT/HA nanocomplexes may serve as glutathione-responsive gene carriers for actively targeting gene delivery to CD44 receptors over-expressed liver cancers.

摘要

细胞内摄取后高效的基因释放对于非病毒基因递送系统非常重要。为构建一种谷胱甘肽响应性基因递送系统,我们在本研究中开发了金-半胱胺(AuCM)/质粒DNA(pDNA)/聚TAT(pTAT)/透明质酸(HA)纳米复合物(AuCM/pDNA/pTAT/HA)。AuCM/pDNA/pTAT/HA纳米复合物尺寸小于200 nm,zeta电位为-17±4 mV,呈阴性。通过紫外可见光谱、表面电荷、动态光散射对多层结构进行了验证,通过透射电子显微镜观察了形态。AuCM/pDNA/pTAT/HA纳米复合物能够完全保护pDNA不被酶降解。这些纳米复合物在HA/CD44相互作用依赖的方式下,在CD44受体过表达的HepG 2细胞中显示出有效的细胞摄取。此外,与AuCM/pDNA/pTAT相比,AuCM/pDNA/pTAT/HA处理的HepG 2细胞转染效率显著提高,并且在谷胱甘肽存在的情况下进一步提高,表明AuCM/pDNA/pTAT/HA具有谷胱甘肽响应性。生物分布显示AuCM/pDNA/pTAT/HA纳米复合物主要积聚在肝脏中。总之,AuCM/pDNA/pTAT/HA纳米复合物可作为谷胱甘肽响应性基因载体,用于将基因主动递送至CD44受体过表达的肝癌细胞。

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