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The Absence of CpG in Plasmid DNA–Chitosan Polyplexes Enhances Transfection Efficiencies and Reduces Inflammatory Responses in Murine Lungs

[Image: see text] Chitosan polyplexes containing plasmid DNA (pDNA) have significant potential for pulmonary gene delivery applications. However, prior to using chitosan/pDNA polyplexes (CSpp) in clinical applications, their potential cytotoxicity needs to be investigated. In this study, we formulat...

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Autores principales: Wongrakpanich, Amaraporn, Adamcakova-Dodd, Andrea, Xie, Wei, Joshi, Vijaya B., Mapuskar, Kranti A., Geary, Sean M., Spitz, Douglas R., Thorne, Peter S., Salem, Aliasger K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3993893/
https://www.ncbi.nlm.nih.gov/pubmed/24494979
http://dx.doi.org/10.1021/mp400689r
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author Wongrakpanich, Amaraporn
Adamcakova-Dodd, Andrea
Xie, Wei
Joshi, Vijaya B.
Mapuskar, Kranti A.
Geary, Sean M.
Spitz, Douglas R.
Thorne, Peter S.
Salem, Aliasger K.
author_facet Wongrakpanich, Amaraporn
Adamcakova-Dodd, Andrea
Xie, Wei
Joshi, Vijaya B.
Mapuskar, Kranti A.
Geary, Sean M.
Spitz, Douglas R.
Thorne, Peter S.
Salem, Aliasger K.
author_sort Wongrakpanich, Amaraporn
collection PubMed
description [Image: see text] Chitosan polyplexes containing plasmid DNA (pDNA) have significant potential for pulmonary gene delivery applications. However, prior to using chitosan/pDNA polyplexes (CSpp) in clinical applications, their potential cytotoxicity needs to be investigated. In this study, we formulated 200–400 nm CSpp with amine to phosphate (N/P) ratios that ranged from 1 to 100. We compared two types of plasmids within CSpp: pDNA that was free of CpG sequences (CpG(−)) and pDNA that contained CpG sequences (CpG(+)). Both forms of CSpp showed low cytotoxicity when cultured with A549 and HEK293 cell lines in vitro. CSpp(CpG(−)) generated higher luciferase expression both in vitro, for A549 cells, and in vivo, compared with CSpp(CpG(+)). In addition, CSpp(CpG(−)) elicited milder inflammatory responses in mice one day subsequent to nasal instillation, as determined by proinflammatory cytokine levels within the bronchoalveolar lavage fluid. Our findings suggest that to achieve optimal gene expression with minimal cytotoxicity, inflammation, and oxidative stress, the N/P ratios and CpG sequences in the pDNA of CSpp need to be considered. These findings will inform the preclinical safety assessments of CSpp in pulmonary gene delivery systems.
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spelling pubmed-39938932015-01-20 The Absence of CpG in Plasmid DNA–Chitosan Polyplexes Enhances Transfection Efficiencies and Reduces Inflammatory Responses in Murine Lungs Wongrakpanich, Amaraporn Adamcakova-Dodd, Andrea Xie, Wei Joshi, Vijaya B. Mapuskar, Kranti A. Geary, Sean M. Spitz, Douglas R. Thorne, Peter S. Salem, Aliasger K. Mol Pharm [Image: see text] Chitosan polyplexes containing plasmid DNA (pDNA) have significant potential for pulmonary gene delivery applications. However, prior to using chitosan/pDNA polyplexes (CSpp) in clinical applications, their potential cytotoxicity needs to be investigated. In this study, we formulated 200–400 nm CSpp with amine to phosphate (N/P) ratios that ranged from 1 to 100. We compared two types of plasmids within CSpp: pDNA that was free of CpG sequences (CpG(−)) and pDNA that contained CpG sequences (CpG(+)). Both forms of CSpp showed low cytotoxicity when cultured with A549 and HEK293 cell lines in vitro. CSpp(CpG(−)) generated higher luciferase expression both in vitro, for A549 cells, and in vivo, compared with CSpp(CpG(+)). In addition, CSpp(CpG(−)) elicited milder inflammatory responses in mice one day subsequent to nasal instillation, as determined by proinflammatory cytokine levels within the bronchoalveolar lavage fluid. Our findings suggest that to achieve optimal gene expression with minimal cytotoxicity, inflammation, and oxidative stress, the N/P ratios and CpG sequences in the pDNA of CSpp need to be considered. These findings will inform the preclinical safety assessments of CSpp in pulmonary gene delivery systems. American Chemical Society 2014-01-20 2014-03-03 /pmc/articles/PMC3993893/ /pubmed/24494979 http://dx.doi.org/10.1021/mp400689r Text en Copyright © 2014 American Chemical Society
spellingShingle Wongrakpanich, Amaraporn
Adamcakova-Dodd, Andrea
Xie, Wei
Joshi, Vijaya B.
Mapuskar, Kranti A.
Geary, Sean M.
Spitz, Douglas R.
Thorne, Peter S.
Salem, Aliasger K.
The Absence of CpG in Plasmid DNA–Chitosan Polyplexes Enhances Transfection Efficiencies and Reduces Inflammatory Responses in Murine Lungs
title The Absence of CpG in Plasmid DNA–Chitosan Polyplexes Enhances Transfection Efficiencies and Reduces Inflammatory Responses in Murine Lungs
title_full The Absence of CpG in Plasmid DNA–Chitosan Polyplexes Enhances Transfection Efficiencies and Reduces Inflammatory Responses in Murine Lungs
title_fullStr The Absence of CpG in Plasmid DNA–Chitosan Polyplexes Enhances Transfection Efficiencies and Reduces Inflammatory Responses in Murine Lungs
title_full_unstemmed The Absence of CpG in Plasmid DNA–Chitosan Polyplexes Enhances Transfection Efficiencies and Reduces Inflammatory Responses in Murine Lungs
title_short The Absence of CpG in Plasmid DNA–Chitosan Polyplexes Enhances Transfection Efficiencies and Reduces Inflammatory Responses in Murine Lungs
title_sort absence of cpg in plasmid dna–chitosan polyplexes enhances transfection efficiencies and reduces inflammatory responses in murine lungs
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3993893/
https://www.ncbi.nlm.nih.gov/pubmed/24494979
http://dx.doi.org/10.1021/mp400689r
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