期刊文献+

SPA-PEI交联物及基于交联物构建的抗体靶向性核酸转移系统对培养细胞的毒性作用

Cytotoxicities of SPA-PEI conjugate and it's antibody-targeted non-virus gene delivery system to cultured cells
原文传递
导出
摘要 目的:评价新型抗体靶向性核酸转移系统及其核心组份[葡萄球菌A蛋白-聚乙烯亚胺交联物(SPAPEI交联物)]对培养细胞的毒性作用。方法:将SPA-PEI交联物与转铁蛋白受体的抗体和绿色荧光蛋白质粒以适宜的质量比混合,组装成一种抗体靶向性核酸转移系统;采用不同浓度SPA-PEI交联物或抗体靶向系统分别处理Hep G2人肝癌细胞不同时间后MTT比色法测定细胞的存活率。结果:SPA-PEI交联物对培养的Hep G2人肝癌毒性作用有明显的浓度依赖性和时间依赖性,但其杀伤效应较PEI降低;抗体靶向系统的细胞毒作用较弱,其作用细胞的存活曲线近似于SPA。结论:SPA-PEI交联物对培养细胞有较强的杀伤效应,但以其为核心组份构建的抗体靶向性核酸转移系统无明显细胞毒性作用。 Objective: To evaluate cytotoxicities of the antibody-targeted non-virus gene delivery system and it's key component[ staphylococcal protein A ( SPA ) - polyethylenimine ( PEI ) conjugate ( SPA- PEI conjugate ) ] to the cultured cells. Methods: One kind of antibody-targeted non-virus gene delivery system was prepared by mixing SPA-PEI conjugate, the enhanced green fluorescent protein plasmid (pEGFP-C1 ) and the transferrin receptor- specific antibody at room temperature for 60 minutes based on their optimal mass ratio. Following incubation with various concentration of the SPA-PEI conjugate or the gene delivery system for different time interval, the cell survivals of cultured HepG2 cells were assayed by MTT colormetric method. Results: SPA-PEI conjugate showed remarkable cytotoxicity to the cells in manner of concentration-dependence and time-dependence, but killing effect was reduce compared with free PEI. However, the antibody-targeted gene delivery system exerted few killing effect on cultured cells,with similar survival curve to free SPA. Conclusion: SPA-PEI conjugate has obvious cytotoxicity to cultured cells, however its antibody-targeted non-virus gene delivery system displays few killing effect.
出处 《现代医学》 2017年第5期631-633,共3页 Modern Medical Journal
基金 四川省教育厅自然科学重点项目(No.13ZA0220)
关键词 葡萄球菌A蛋白-聚乙烯亚胺交联物 抗体靶向 细胞毒性 staphylococcal protein A- polyethylenimine conjugate antibody- targeted cytotoxicity
  • 相关文献

参考文献5

二级参考文献97

  • 1叶树楠,杨述华,杨操,许伟华.肿瘤靶向性载体介导的IL-12基因增强裸鼠抗骨肉瘤免疫[J].肿瘤防治研究,2005,32(5):305-307. 被引量:2
  • 2李达,王青青,余海.基于聚乙烯亚胺为骨架的非病毒转基因载体的构建策略[J].国际肿瘤学杂志,2006,33(3):167-170. 被引量:5
  • 3刘晓波,余学清,李晓艳,董秀清.CD44抗体靶向绿色荧光蛋白质粒导入系统的构建及其特异性转染大鼠肾小管上皮细胞的观察[J].中国病理生理杂志,2006,22(6):1232-1234. 被引量:4
  • 4Zhang Y, Jeong Lee H, Boado RJ, et al. Receptoor-mexhated delivery of an antisense gene to human brain cancer cells[J]. J Gene Med, 2002, 4(2): 183- 194.
  • 5Drummond DC, Meyer O, Hong K, et al.Optimizing liposomes for delivery of chemotherapeutic agents to solid tumors[J]. Pharmacol Rev, 1999, 51(4):691-743.
  • 6Harada-Shiba M, Yamauchi K, Harada A, et al. Polyion complex micelles as vectors in gene therapy - pharmacokinetics and in vivo gene transfer[J]. Gene Ther, 2002, 9(6):407-414.
  • 7Kircheis R, Ostermann E, Wolscher ME et al.Tumor-targeted gene delivery of tumor necrosis factor-alpha induces tumor necrosis and tumor regression without systemic toxicity[j]. Cancer Gene. Ther, 2002. 9(8):675-680.
  • 8Ogris M, Steinlein P, Carotta S, et al. DNA/polyethylenimme transfection particles refluence of ligands, polymer size, and PEGylation on internalization and gene expression [J] . AAPS Pharm Sci , 2001,302:F21.
  • 9Kircheis R, Wightman L, Schreiber et al.polyethylenimine /DNA complexes shielder by transperrin target gene expression to tumors after system application[J].Gene Ther, 2001 , 8( 1 ) :28 - 40.
  • 10Lemieux P,Vinogradov SV ,Gebhart CL , et al. Block and graft copolymers and NanoGel Copolymer networks for DNA delivery into cell[J].J Drug Target 2000, 8 ( 2 ) : 91 -105.

共引文献12

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部