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Multidisciplinary Approach to the Transfection of Plasmid DNA by a Nonviral Nanocarrier Based on a Gemini–Bolaamphiphilic Hybrid Lipid

[Image: see text] A multidisciplinary strategy, including both biochemical and biophysical studies, was proposed here to evaluate the potential of lipid nanoaggregates consisting of a mixture of a gemini–bolaamphiphilic lipid (C(6)C(22)C(6)) and the well-known helper lipid 1,2-dioleoyl-sn-glycero-3-...

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Autores principales: Martínez-Negro, María, Guerrero-Martínez, Andrés, García-Río, Luis, Domènech, Òscar, Aicart, Emilio, Tros de Ilarduya, Conchita, Junquera, Elena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044976/
https://www.ncbi.nlm.nih.gov/pubmed/30023772
http://dx.doi.org/10.1021/acsomega.7b01657
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author Martínez-Negro, María
Guerrero-Martínez, Andrés
García-Río, Luis
Domènech, Òscar
Aicart, Emilio
Tros de Ilarduya, Conchita
Junquera, Elena
author_facet Martínez-Negro, María
Guerrero-Martínez, Andrés
García-Río, Luis
Domènech, Òscar
Aicart, Emilio
Tros de Ilarduya, Conchita
Junquera, Elena
author_sort Martínez-Negro, María
collection PubMed
description [Image: see text] A multidisciplinary strategy, including both biochemical and biophysical studies, was proposed here to evaluate the potential of lipid nanoaggregates consisting of a mixture of a gemini–bolaamphiphilic lipid (C(6)C(22)C(6)) and the well-known helper lipid 1,2-dioleoyl-sn-glycero-3-phosphatidylethanolamine (DOPE) to transfect plasmid DNA into living cells in an efficient and safe way. For that purpose, several experimental techniques were employed, such as zeta potential (phase analysis light scattering methodology), agarose gel electrophoresis (pDNA compaction and pDNA protection assays), small-angle X-ray scattering, cryo-transmission electron microscopy, atomic force microscopy, fluorescence-assisted cell sorting, luminometry, and cytotoxicity assays. The results revealed that the cationic lipid and plasmid offer only 70 and 30% of their nominal positive ([Image: see text]) and negative charges ([Image: see text]), respectively. Upon mixing with DOPE, they form lipoplexes that self-aggregate in typical multilamellar L(α) lyotropic liquid-crystal nanostructures with sizes in the range of 100–200 nm and low polydispersities, very suitably fitted to remain in the bloodstream and cross the cell membrane. Interestingly, these nanoaggregates were able to compact, protect (from the degrading effect of DNase I), and transfect two DNA plasmids (pEGFP-C3, encoding the green fluorescent protein, and pCMV-Luc, encoding luciferase) into COS-7 cells, with an efficiency equal or even superior to that of the universal control Lipo2000*, as long as the effective +/– charge ratio was maintained higher than 1 but reasonably close to electroneutrality. Moreover, this transfection process was not cytotoxic because the viability of COS-7 cells remained at high levels, greater than 80%. All of these features make the C(6)C(22)C(6)/DOPE nanosystem an optimal nonviral gene nanocarrier in vitro and a potentially interesting candidate for future in vivo experiments.
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spelling pubmed-60449762018-07-16 Multidisciplinary Approach to the Transfection of Plasmid DNA by a Nonviral Nanocarrier Based on a Gemini–Bolaamphiphilic Hybrid Lipid Martínez-Negro, María Guerrero-Martínez, Andrés García-Río, Luis Domènech, Òscar Aicart, Emilio Tros de Ilarduya, Conchita Junquera, Elena ACS Omega [Image: see text] A multidisciplinary strategy, including both biochemical and biophysical studies, was proposed here to evaluate the potential of lipid nanoaggregates consisting of a mixture of a gemini–bolaamphiphilic lipid (C(6)C(22)C(6)) and the well-known helper lipid 1,2-dioleoyl-sn-glycero-3-phosphatidylethanolamine (DOPE) to transfect plasmid DNA into living cells in an efficient and safe way. For that purpose, several experimental techniques were employed, such as zeta potential (phase analysis light scattering methodology), agarose gel electrophoresis (pDNA compaction and pDNA protection assays), small-angle X-ray scattering, cryo-transmission electron microscopy, atomic force microscopy, fluorescence-assisted cell sorting, luminometry, and cytotoxicity assays. The results revealed that the cationic lipid and plasmid offer only 70 and 30% of their nominal positive ([Image: see text]) and negative charges ([Image: see text]), respectively. Upon mixing with DOPE, they form lipoplexes that self-aggregate in typical multilamellar L(α) lyotropic liquid-crystal nanostructures with sizes in the range of 100–200 nm and low polydispersities, very suitably fitted to remain in the bloodstream and cross the cell membrane. Interestingly, these nanoaggregates were able to compact, protect (from the degrading effect of DNase I), and transfect two DNA plasmids (pEGFP-C3, encoding the green fluorescent protein, and pCMV-Luc, encoding luciferase) into COS-7 cells, with an efficiency equal or even superior to that of the universal control Lipo2000*, as long as the effective +/– charge ratio was maintained higher than 1 but reasonably close to electroneutrality. Moreover, this transfection process was not cytotoxic because the viability of COS-7 cells remained at high levels, greater than 80%. All of these features make the C(6)C(22)C(6)/DOPE nanosystem an optimal nonviral gene nanocarrier in vitro and a potentially interesting candidate for future in vivo experiments. American Chemical Society 2018-01-08 /pmc/articles/PMC6044976/ /pubmed/30023772 http://dx.doi.org/10.1021/acsomega.7b01657 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Martínez-Negro, María
Guerrero-Martínez, Andrés
García-Río, Luis
Domènech, Òscar
Aicart, Emilio
Tros de Ilarduya, Conchita
Junquera, Elena
Multidisciplinary Approach to the Transfection of Plasmid DNA by a Nonviral Nanocarrier Based on a Gemini–Bolaamphiphilic Hybrid Lipid
title Multidisciplinary Approach to the Transfection of Plasmid DNA by a Nonviral Nanocarrier Based on a Gemini–Bolaamphiphilic Hybrid Lipid
title_full Multidisciplinary Approach to the Transfection of Plasmid DNA by a Nonviral Nanocarrier Based on a Gemini–Bolaamphiphilic Hybrid Lipid
title_fullStr Multidisciplinary Approach to the Transfection of Plasmid DNA by a Nonviral Nanocarrier Based on a Gemini–Bolaamphiphilic Hybrid Lipid
title_full_unstemmed Multidisciplinary Approach to the Transfection of Plasmid DNA by a Nonviral Nanocarrier Based on a Gemini–Bolaamphiphilic Hybrid Lipid
title_short Multidisciplinary Approach to the Transfection of Plasmid DNA by a Nonviral Nanocarrier Based on a Gemini–Bolaamphiphilic Hybrid Lipid
title_sort multidisciplinary approach to the transfection of plasmid dna by a nonviral nanocarrier based on a gemini–bolaamphiphilic hybrid lipid
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044976/
https://www.ncbi.nlm.nih.gov/pubmed/30023772
http://dx.doi.org/10.1021/acsomega.7b01657
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