Efficient gene delivery to human umbilical cord mesenchymal stem cells by cationized Porphyra yezoensis polysaccharide nanoparticles

被引:25
|
作者
Yu, Qingtong [1 ,2 ,3 ]
Cao, Jin [2 ,3 ]
Chen, Baoding [4 ]
Deng, Wenwen [2 ,3 ]
Cao, Xia [2 ,3 ]
Chen, Jingjing [2 ,3 ]
Wang, Yan [2 ,3 ]
Wang, Shicheng [2 ,3 ]
Yu, Jiangnan [2 ,3 ]
Xu, Ximing [2 ,3 ]
Gao, Xiangdong [1 ]
机构
[1] China Pharmaceut Univ, Sch Life Sci & Technol, Nanjing 210009, Jiangsu, Peoples R China
[2] Jiangsu Univ, Dept Pharmaceut, Sch Pharm, Zhenjiang 212001, Jiangsu, Peoples R China
[3] Jiangsu Univ, Ctr Drug Gene Delivery & Tissue Engn, Zhenjiang 212001, Jiangsu, Peoples R China
[4] Jiangsu Univ, Affiliated Hosp, Dept Med Ultrasound, Zhenjiang 212001, Jiangsu, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
Porphyra yezoensis; nanoparticle; nonviral vector; human umbilical cord mesenchymal stem cells; Wnt3a; IN-VITRO; PLASMID; GENERATION; CARRIERS; NORI; PROLIFERATION; ANTIOXIDANT; INDUCTION; LIPOSOMES; CHITOSAN;
D O I
10.2147/IJN.S93122
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
This study centered on an innovative application of Porphyra yezoensis polysaccharide (PPS) with cationic modification as a safe and efficient nonviral gene vector to deliver a plasmid encoding human Wnt3a (pWnt3a) into human umbilical cord mesenchymal stem cells (HUMSCs). After modification with branched low-molecular-weight (1,200 Da) polyethylenimine, the cationized PPS (CPPS) was combined with pWnt3a to form spherical nanoscale particles (CPPS-pWnt3a nanoparticles). Particle size and distribution indicated that the CPPS-pWnt3a nanoparticles at a CPPS: pWnt3a weight ratio of 40: 1 might be a potential candidate for DNA plasmid transfection. A cytotoxicity assay demonstrated that the nanoparticles prepared at a CPPS: pWnt3a weight ratio of 40: 1 were nontoxic to HUMSCs compared to those of Lipofectamine 2000 and polyethylenimine (25 kDa). These nanoparticles were further transfected to HUMSCs. Western blotting demonstrated that the nanoparticles (CPPS: pWnt3a weight ratio 40: 1) had the greatest transfection efficiency in HUMSCs, which was significantly higher than that of Lipofectamine 2000; however, when the CPPS: pWnt3a weight ratio was increased to 80: 1, the nanoparticle-treated group showed no obvious improvement in translation efficiency over Lipofectamine 2000. Therefore, CPPS, a novel cationic polysaccharide derived from P. yezoensis, could be developed into a safe, efficient, nonviral gene vector in a gene-delivery system.
引用
收藏
页码:7097 / 7107
页数:11
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