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

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 br...

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Autores principales: Yu, Qingtong, Cao, Jin, Chen, Baoding, Deng, Wenwen, Cao, Xia, Chen, Jingjing, Wang, Yan, Wang, Shicheng, Yu, Jiangnan, Xu, Ximing, Gao, Xiangdong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4655959/
https://www.ncbi.nlm.nih.gov/pubmed/26604758
http://dx.doi.org/10.2147/IJN.S93122
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author Yu, Qingtong
Cao, Jin
Chen, Baoding
Deng, Wenwen
Cao, Xia
Chen, Jingjing
Wang, Yan
Wang, Shicheng
Yu, Jiangnan
Xu, Ximing
Gao, Xiangdong
author_facet Yu, Qingtong
Cao, Jin
Chen, Baoding
Deng, Wenwen
Cao, Xia
Chen, Jingjing
Wang, Yan
Wang, Shicheng
Yu, Jiangnan
Xu, Ximing
Gao, Xiangdong
author_sort Yu, Qingtong
collection PubMed
description 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.
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spelling pubmed-46559592015-11-24 Efficient gene delivery to human umbilical cord mesenchymal stem cells by cationized Porphyra yezoensis polysaccharide nanoparticles Yu, Qingtong Cao, Jin Chen, Baoding Deng, Wenwen Cao, Xia Chen, Jingjing Wang, Yan Wang, Shicheng Yu, Jiangnan Xu, Ximing Gao, Xiangdong Int J Nanomedicine Original Research 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. Dove Medical Press 2015-11-18 /pmc/articles/PMC4655959/ /pubmed/26604758 http://dx.doi.org/10.2147/IJN.S93122 Text en © 2015 Yu et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Yu, Qingtong
Cao, Jin
Chen, Baoding
Deng, Wenwen
Cao, Xia
Chen, Jingjing
Wang, Yan
Wang, Shicheng
Yu, Jiangnan
Xu, Ximing
Gao, Xiangdong
Efficient gene delivery to human umbilical cord mesenchymal stem cells by cationized Porphyra yezoensis polysaccharide nanoparticles
title Efficient gene delivery to human umbilical cord mesenchymal stem cells by cationized Porphyra yezoensis polysaccharide nanoparticles
title_full Efficient gene delivery to human umbilical cord mesenchymal stem cells by cationized Porphyra yezoensis polysaccharide nanoparticles
title_fullStr Efficient gene delivery to human umbilical cord mesenchymal stem cells by cationized Porphyra yezoensis polysaccharide nanoparticles
title_full_unstemmed Efficient gene delivery to human umbilical cord mesenchymal stem cells by cationized Porphyra yezoensis polysaccharide nanoparticles
title_short Efficient gene delivery to human umbilical cord mesenchymal stem cells by cationized Porphyra yezoensis polysaccharide nanoparticles
title_sort efficient gene delivery to human umbilical cord mesenchymal stem cells by cationized porphyra yezoensis polysaccharide nanoparticles
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4655959/
https://www.ncbi.nlm.nih.gov/pubmed/26604758
http://dx.doi.org/10.2147/IJN.S93122
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