Transfection of bovine fetal fibroblast with polyethylenimine (PEI) nanoparticles: effect of particle size and presence of fetal bovine serum on transgene delivery and cytotoxicity

被引:17
作者
Forcato, D. O. [1 ,2 ]
Fili, A. E. [1 ,2 ]
Alustiza, F. E. [2 ,3 ]
Lazaro Martinez, J. M. [2 ,4 ]
Bongiovanni Abel, S. [2 ,3 ]
Olmos Nicotra, M. F. [1 ,2 ]
Alessio, A. P. [1 ,2 ]
Rodriguez, N. [1 ]
Barbero, C. [3 ]
Bosch, P. [1 ,2 ]
机构
[1] Univ Nacl Rio Cuarto, FCEFQyN, Dept Mol Biol, Cordoba, Argentina
[2] Consejo Nacl Invest Cient & Tecn, Buenos Aires, DF, Argentina
[3] Univ Nacl Rio Cuarto, FCEFQyN, Dept Chem, Cordoba, Argentina
[4] Univ Buenos Aires, IQUIFIB FFyB, Buenos Aires, DF, Argentina
关键词
Transgenesis; Cattle; Fibroblasts; Polyethylenimine; Cell transfection; LOW-MOLECULAR-WEIGHT; GENE DELIVERY; LINEAR POLYETHYLENIMINE; NONVIRAL VECTORS; IN-VITRO; EFFICIENCY; POLY(ETHYLENIMINE); COMPLEXES; DESIGN; CELLS;
D O I
10.1007/s10616-017-0075-6
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The development of efficient transfection protocols for livestock cells is crucial for implementation of cell-based transgenic methods to produce genetically modified animals. We synthetized fully deacylated linear 22, 87 and 217 kDa polyethylenimine (PEI) nanoparticles and compared their transfection efficiency and cytotoxicity to commercial branched 25 kDa PEI and linear 58 kDa poly(allylamine) hydrochloride. We studied the effect of PEI size and presence of serum on transfection efficiency on primary cultures of bovine fetal fibroblasts and established cells lines (HEK 293 and Hep G2). We found that transfection efficiency was affected mainly by polymer/pDNA ratio and DNA concentration and in less extent by PEI MW. In bovine fibroblast, preincubation of PEI nanoparticles with fetal bovine serum (FBS) greatly increased percentage of cells expressing the transgene (up to 82%) while significantly decreased the polymer cytotoxic effect. 87 and 217 kDa PEI rendered the highest transfection rates in HEK 293 and Hep G2 cell lines (>50% transfected cells) with minimal cell toxicity. In conclusion, our results indicate that fully deacylated PEI of 87 and 217 kDa are useful DNA vehicles for non-viral transfection of primary cultures of bovine fetal fibroblast and HEK 293 and Hep G2 cell lines.
引用
收藏
页码:655 / 665
页数:11
相关论文
共 34 条
[11]  
2-Q
[12]   Optimization of 25 kDa linear polyethylenimine for efficient gene delivery [J].
Huh, Sun-Hyung ;
Do, Hyun-Jin ;
Lim, Hye-Young ;
Kim, Dong-Ku ;
Choi, Seong-Jun ;
Song, Hyuk ;
Kim, Nam-Hyung ;
Park, Jin-Ki ;
Chang, Won-Kyong ;
Chung, Hyung-Min ;
Kim, Jae-Hwan .
BIOLOGICALS, 2007, 35 (03) :165-171
[13]   Molecular hurdles in polyfectin design and mechanistic background to polycation induced cytotoxicity [J].
Hunter, A. Christy .
ADVANCED DRUG DELIVERY REVIEWS, 2006, 58 (14) :1523-1531
[14]   DNA transfection using linear poly(ethylenimine) prepared by controlled acid hydrolysis of poly(2-ethyl-2-oxazoline) [J].
Jeong, JH ;
Song, SH ;
Lim, DW ;
Lee, H ;
Park, TG .
JOURNAL OF CONTROLLED RELEASE, 2001, 73 (2-3) :391-399
[15]   Optimized dextran-polyethylenimine conjugates are efficient non-viral vectors with reduced cytotoxicity when used in serum containing environments [J].
Jiang, Dahai ;
Salem, Aliasger K. .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2012, 427 (01) :71-79
[16]   Evaluation of proinflammatory cytokine production induced by linear and branched polyethylenimine/plasmid DNA complexes in mice [J].
Kawakami, Shigeru ;
Ito, Yoshitaka ;
Charoensit, Pensri ;
Yamashita, Fumiyoshi ;
Hashida, Mitsuru .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2006, 317 (03) :1382-1390
[17]   Gene transfer with modified polyethylenimines [J].
Kichler, A .
JOURNAL OF GENE MEDICINE, 2004, 6 :S3-S10
[18]   Pluronic/Polyethylenimine Shell Cross linked Nanocapsules with Embedded Magnetite Nanocrystals for Magnetically Triggered Delivery of siRNA [J].
Lee, Kyuri ;
Bae, Ki Hyun ;
Lee, Yuhan ;
Lee, Soo Hyeon ;
Ahn, Cheol-Hee ;
Park, Tae Gwan .
MACROMOLECULAR BIOSCIENCE, 2010, 10 (03) :239-245
[19]  
Liang W., 2012, MOL REGULATION ENDOC, P421
[20]   Polyethylenimine-based non-viral gene delivery systems [J].
Lungwitz, U ;
Breunig, M ;
Blunk, T ;
Göpferich, A .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2005, 60 (02) :247-266