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Bioreducible Liposomes for Gene Delivery: From the Formulation to the Mechanism of Action

BACKGROUND: A promising strategy to create stimuli-responsive gene delivery systems is to exploit the redox gradient between the oxidizing extracellular milieu and the reducing cytoplasm in order to disassemble DNA/cationic lipid complexes (lipoplexes). On these premises, we previously described the...

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Autores principales: Candiani, Gabriele, Pezzoli, Daniele, Ciani, Laura, Chiesa, Roberto, Ristori, Sandra
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2955545/
https://www.ncbi.nlm.nih.gov/pubmed/20976172
http://dx.doi.org/10.1371/journal.pone.0013430
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author Candiani, Gabriele
Pezzoli, Daniele
Ciani, Laura
Chiesa, Roberto
Ristori, Sandra
author_facet Candiani, Gabriele
Pezzoli, Daniele
Ciani, Laura
Chiesa, Roberto
Ristori, Sandra
author_sort Candiani, Gabriele
collection PubMed
description BACKGROUND: A promising strategy to create stimuli-responsive gene delivery systems is to exploit the redox gradient between the oxidizing extracellular milieu and the reducing cytoplasm in order to disassemble DNA/cationic lipid complexes (lipoplexes). On these premises, we previously described the synthesis of SS14 redox-sensitive gemini surfactant for gene delivery. Although others have attributed the beneficial effects of intracellular reducing environment to reduced glutathione (GSH), these observations cannot rule out the possible implication of the redox milieu in its whole on transfection efficiency of bioreducible transfectants leaving the determinants of DNA release largely undefined. METHODOLOGY/PRINCIPAL FINDINGS: With the aim of addressing this issue, SS14 was here formulated into binary and ternary 100 nm-extruded liposomes and the effects of the helper lipid composition and of the SS14/helper lipids molar ratio on chemical-physical and structural parameters defining transfection effectiveness were investigated. Among all formulations tested, DOPC/DOPE/SS14 at 25∶50∶25 molar ratio was the most effective in transfection studies owing to the presence of dioleoyl chains and phosphatidylethanolamine head groups in co-lipids. The increase in SS14 content up to 50% along DOPC/DOPE/SS14 liposome series yielded enhanced transfection, up to 2.7-fold higher than that of the benchmark Lipofectamine 2000, without altering cytotoxicity of the corresponding lipoplexes at charge ratio 5. Secondly, we specifically investigated the redox-dependent mechanisms of gene delivery into cells through tailored protocols of transfection in GSH-depleted and repleted vs. increased oxidative stress conditions. Importantly, GSH specifically induced DNA release in batch and in vitro. CONCLUSIONS/SIGNIFICANCE: The presence of helper lipids carrying unsaturated dioleoyl chains and phosphatidylethanolamine head groups significantly improved transfection efficiencies of DOPC/DOPE/SS14 lipoplexes. Most importantly, this study shows that intracellular GSH levels linearly correlated with transfection efficiency while oxidative stress levels did not, highlighting for the first time the pivotal role of GSH rather than oxidative stress in its whole in transfection of bioreducible vectors.
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spelling pubmed-29555452010-10-25 Bioreducible Liposomes for Gene Delivery: From the Formulation to the Mechanism of Action Candiani, Gabriele Pezzoli, Daniele Ciani, Laura Chiesa, Roberto Ristori, Sandra PLoS One Research Article BACKGROUND: A promising strategy to create stimuli-responsive gene delivery systems is to exploit the redox gradient between the oxidizing extracellular milieu and the reducing cytoplasm in order to disassemble DNA/cationic lipid complexes (lipoplexes). On these premises, we previously described the synthesis of SS14 redox-sensitive gemini surfactant for gene delivery. Although others have attributed the beneficial effects of intracellular reducing environment to reduced glutathione (GSH), these observations cannot rule out the possible implication of the redox milieu in its whole on transfection efficiency of bioreducible transfectants leaving the determinants of DNA release largely undefined. METHODOLOGY/PRINCIPAL FINDINGS: With the aim of addressing this issue, SS14 was here formulated into binary and ternary 100 nm-extruded liposomes and the effects of the helper lipid composition and of the SS14/helper lipids molar ratio on chemical-physical and structural parameters defining transfection effectiveness were investigated. Among all formulations tested, DOPC/DOPE/SS14 at 25∶50∶25 molar ratio was the most effective in transfection studies owing to the presence of dioleoyl chains and phosphatidylethanolamine head groups in co-lipids. The increase in SS14 content up to 50% along DOPC/DOPE/SS14 liposome series yielded enhanced transfection, up to 2.7-fold higher than that of the benchmark Lipofectamine 2000, without altering cytotoxicity of the corresponding lipoplexes at charge ratio 5. Secondly, we specifically investigated the redox-dependent mechanisms of gene delivery into cells through tailored protocols of transfection in GSH-depleted and repleted vs. increased oxidative stress conditions. Importantly, GSH specifically induced DNA release in batch and in vitro. CONCLUSIONS/SIGNIFICANCE: The presence of helper lipids carrying unsaturated dioleoyl chains and phosphatidylethanolamine head groups significantly improved transfection efficiencies of DOPC/DOPE/SS14 lipoplexes. Most importantly, this study shows that intracellular GSH levels linearly correlated with transfection efficiency while oxidative stress levels did not, highlighting for the first time the pivotal role of GSH rather than oxidative stress in its whole in transfection of bioreducible vectors. Public Library of Science 2010-10-15 /pmc/articles/PMC2955545/ /pubmed/20976172 http://dx.doi.org/10.1371/journal.pone.0013430 Text en Candiani et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Candiani, Gabriele
Pezzoli, Daniele
Ciani, Laura
Chiesa, Roberto
Ristori, Sandra
Bioreducible Liposomes for Gene Delivery: From the Formulation to the Mechanism of Action
title Bioreducible Liposomes for Gene Delivery: From the Formulation to the Mechanism of Action
title_full Bioreducible Liposomes for Gene Delivery: From the Formulation to the Mechanism of Action
title_fullStr Bioreducible Liposomes for Gene Delivery: From the Formulation to the Mechanism of Action
title_full_unstemmed Bioreducible Liposomes for Gene Delivery: From the Formulation to the Mechanism of Action
title_short Bioreducible Liposomes for Gene Delivery: From the Formulation to the Mechanism of Action
title_sort bioreducible liposomes for gene delivery: from the formulation to the mechanism of action
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2955545/
https://www.ncbi.nlm.nih.gov/pubmed/20976172
http://dx.doi.org/10.1371/journal.pone.0013430
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