Increased gene delivery efficiency and specificity of a lipid-based nanosystem incorporating a glycolipid

Mariana Magalhães,1,2,* Dina Farinha,1,* Maria Conceição Pedroso de Lima,1,2 Henrique Faneca1 1Center for Neuroscience and Cell Biology, University of Coimbra, Coimbra, Portugal; 2Department of Life Sciences, Faculty of Science and Technology, University of Coimbra...

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Autores principales: Magalhães M, Farinha D, Pedroso de Lima MC, Faneca H
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Publicado: Dove Medical Press 2014
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spelling oai:doaj.org-article:856fe83867984e0e92b8599d777e5da02021-12-02T02:10:33ZIncreased gene delivery efficiency and specificity of a lipid-based nanosystem incorporating a glycolipid1178-2013https://doaj.org/article/856fe83867984e0e92b8599d777e5da02014-10-01T00:00:00Zhttp://www.dovepress.com/increased-gene-delivery-efficiency-and-specificity-of-a-lipid-based-na-peer-reviewed-article-IJNhttps://doaj.org/toc/1178-2013 Mariana Magalhães,1,2,* Dina Farinha,1,* Maria Conceição Pedroso de Lima,1,2 Henrique Faneca1 1Center for Neuroscience and Cell Biology, University of Coimbra, Coimbra, Portugal; 2Department of Life Sciences, Faculty of Science and Technology, University of Coimbra, Coimbra, Portugal *These authors contributed equally to this work Abstract: Hepatocellular carcinoma (HCC) is the third most common cause of death related to cancer diseases worldwide. The current treatment options have many limitations and reduced success rates. In this regard, advances in gene therapy have shown promising results in novel therapeutic strategies. However, the success of gene therapy depends on the efficient and specific delivery of genetic material into target cells. In this regard, the main goal of this work was to develop a new lipid-based nanosystem formulation containing the lipid lactosyl-PE for specific and efficient gene delivery into HCC cells. The obtained results showed that incorporation of 15% of lactosyl-PE into liposomes induces a strong potentiation of lipoplex biological activity in HepG2 cells, not only in terms of transgene expression levels but also in terms of percentage of transfected cells. In the presence of galactose, which competes with lactosyl-PE for the binding to the asialoglycoprotein receptor (ASGP-R), a significant reduction in biological activity was observed, showing that the potentiation of transfection induced by the presence of lactosyl-PE could be due to its specific interaction with ASGP-R, which is overexpressed in HCC. In addition, it was found that the incorporation of lactosyl-PE in the nanosystems promotes an increase in their cell binding and uptake. Regarding the physicochemical properties of lipoplexes, the presence of lactosyl-PE resulted in a significant increase in DNA protection and in a substantial decrease in their mean diameter and zeta potential, conferring them suitable characteristics for in vivo application. Overall, the results obtained in this study suggest that the potentiation of the biological activity induced by the presence of lactosyl-PE is due to its specific binding to the ASGP-R, showing that this novel formulation could constitute a new gene delivery nanosystem for application in therapeutic strategies in HCC. Keywords: targeted gene delivery, hepatocellular carcinoma, lactosyl-PE, cationic liposomes, gene delivery nanosystemsMagalhães MFarinha DPedroso de Lima MCFaneca HDove Medical PressarticleMedicine (General)R5-920ENInternational Journal of Nanomedicine, Vol 2014, Iss Issue 1, Pp 4979-4989 (2014)
institution DOAJ
collection DOAJ
language EN
topic Medicine (General)
R5-920
spellingShingle Medicine (General)
R5-920
Magalhães M
Farinha D
Pedroso de Lima MC
Faneca H
Increased gene delivery efficiency and specificity of a lipid-based nanosystem incorporating a glycolipid
description Mariana Magalhães,1,2,* Dina Farinha,1,* Maria Conceição Pedroso de Lima,1,2 Henrique Faneca1 1Center for Neuroscience and Cell Biology, University of Coimbra, Coimbra, Portugal; 2Department of Life Sciences, Faculty of Science and Technology, University of Coimbra, Coimbra, Portugal *These authors contributed equally to this work Abstract: Hepatocellular carcinoma (HCC) is the third most common cause of death related to cancer diseases worldwide. The current treatment options have many limitations and reduced success rates. In this regard, advances in gene therapy have shown promising results in novel therapeutic strategies. However, the success of gene therapy depends on the efficient and specific delivery of genetic material into target cells. In this regard, the main goal of this work was to develop a new lipid-based nanosystem formulation containing the lipid lactosyl-PE for specific and efficient gene delivery into HCC cells. The obtained results showed that incorporation of 15% of lactosyl-PE into liposomes induces a strong potentiation of lipoplex biological activity in HepG2 cells, not only in terms of transgene expression levels but also in terms of percentage of transfected cells. In the presence of galactose, which competes with lactosyl-PE for the binding to the asialoglycoprotein receptor (ASGP-R), a significant reduction in biological activity was observed, showing that the potentiation of transfection induced by the presence of lactosyl-PE could be due to its specific interaction with ASGP-R, which is overexpressed in HCC. In addition, it was found that the incorporation of lactosyl-PE in the nanosystems promotes an increase in their cell binding and uptake. Regarding the physicochemical properties of lipoplexes, the presence of lactosyl-PE resulted in a significant increase in DNA protection and in a substantial decrease in their mean diameter and zeta potential, conferring them suitable characteristics for in vivo application. Overall, the results obtained in this study suggest that the potentiation of the biological activity induced by the presence of lactosyl-PE is due to its specific binding to the ASGP-R, showing that this novel formulation could constitute a new gene delivery nanosystem for application in therapeutic strategies in HCC. Keywords: targeted gene delivery, hepatocellular carcinoma, lactosyl-PE, cationic liposomes, gene delivery nanosystems
format article
author Magalhães M
Farinha D
Pedroso de Lima MC
Faneca H
author_facet Magalhães M
Farinha D
Pedroso de Lima MC
Faneca H
author_sort Magalhães M
title Increased gene delivery efficiency and specificity of a lipid-based nanosystem incorporating a glycolipid
title_short Increased gene delivery efficiency and specificity of a lipid-based nanosystem incorporating a glycolipid
title_full Increased gene delivery efficiency and specificity of a lipid-based nanosystem incorporating a glycolipid
title_fullStr Increased gene delivery efficiency and specificity of a lipid-based nanosystem incorporating a glycolipid
title_full_unstemmed Increased gene delivery efficiency and specificity of a lipid-based nanosystem incorporating a glycolipid
title_sort increased gene delivery efficiency and specificity of a lipid-based nanosystem incorporating a glycolipid
publisher Dove Medical Press
publishDate 2014
url https://doaj.org/article/856fe83867984e0e92b8599d777e5da0
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AT pedrosodelimamc increasedgenedeliveryefficiencyandspecificityofalipidbasednanosystemincorporatingaglycolipid
AT fanecah increasedgenedeliveryefficiencyandspecificityofalipidbasednanosystemincorporatingaglycolipid
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