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Electroporation-Mediated Gene Transfer Directly to the Swine Heart

In vivo gene transfer to the ischemic heart via electroporation holds promise as a potential therapeutic approach for the treatment of heart disease. In the current study, we investigated the use of in vivo electroporation for gene transfer using 3 different penetrating electrodes and one non-penetr...

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Autores principales: Hargrave, Barbara, Downey, Harre, Strange, Robert, Murray, Len, Cinnamond, Cade, Lundberg, Cathryn, Israel, Annelise, Chen, Yeong-Jer, Marshall, William, Heller, Richard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3387511/
https://www.ncbi.nlm.nih.gov/pubmed/22456328
http://dx.doi.org/10.1038/gt.2012.15
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author Hargrave, Barbara
Downey, Harre
Strange, Robert
Murray, Len
Cinnamond, Cade
Lundberg, Cathryn
Israel, Annelise
Chen, Yeong-Jer
Marshall, William
Heller, Richard
author_facet Hargrave, Barbara
Downey, Harre
Strange, Robert
Murray, Len
Cinnamond, Cade
Lundberg, Cathryn
Israel, Annelise
Chen, Yeong-Jer
Marshall, William
Heller, Richard
author_sort Hargrave, Barbara
collection PubMed
description In vivo gene transfer to the ischemic heart via electroporation holds promise as a potential therapeutic approach for the treatment of heart disease. In the current study, we investigated the use of in vivo electroporation for gene transfer using 3 different penetrating electrodes and one non-penetrating electrode. The hearts of adult male swine were exposed through a sternotomy. Eight electric pulses synchronized to the rising phase of the R wave of the ECG were administered at varying pulse widths and field strengths following an injection of either a plasmid encoding luciferase or one encoding green fluorescent protein. Four sites on the anterior wall of the left ventricle were treated. Animals were euthanized 48 hours after injection and electroporation and gene expression was determined. Results were compared to sites in the heart that received plasmid injection but no electric pulses or were not treated. Gene expression was higher in all electroporated sites when compared to injection only sites demonstrating the robustness of this approach. Our results provide evidence that in vivo electroporation can be a safe and effective non-viral method for delivering genes to the heart, in vivo.
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spelling pubmed-33875112013-08-01 Electroporation-Mediated Gene Transfer Directly to the Swine Heart Hargrave, Barbara Downey, Harre Strange, Robert Murray, Len Cinnamond, Cade Lundberg, Cathryn Israel, Annelise Chen, Yeong-Jer Marshall, William Heller, Richard Gene Ther Article In vivo gene transfer to the ischemic heart via electroporation holds promise as a potential therapeutic approach for the treatment of heart disease. In the current study, we investigated the use of in vivo electroporation for gene transfer using 3 different penetrating electrodes and one non-penetrating electrode. The hearts of adult male swine were exposed through a sternotomy. Eight electric pulses synchronized to the rising phase of the R wave of the ECG were administered at varying pulse widths and field strengths following an injection of either a plasmid encoding luciferase or one encoding green fluorescent protein. Four sites on the anterior wall of the left ventricle were treated. Animals were euthanized 48 hours after injection and electroporation and gene expression was determined. Results were compared to sites in the heart that received plasmid injection but no electric pulses or were not treated. Gene expression was higher in all electroporated sites when compared to injection only sites demonstrating the robustness of this approach. Our results provide evidence that in vivo electroporation can be a safe and effective non-viral method for delivering genes to the heart, in vivo. 2012-03-29 2013-02 /pmc/articles/PMC3387511/ /pubmed/22456328 http://dx.doi.org/10.1038/gt.2012.15 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Hargrave, Barbara
Downey, Harre
Strange, Robert
Murray, Len
Cinnamond, Cade
Lundberg, Cathryn
Israel, Annelise
Chen, Yeong-Jer
Marshall, William
Heller, Richard
Electroporation-Mediated Gene Transfer Directly to the Swine Heart
title Electroporation-Mediated Gene Transfer Directly to the Swine Heart
title_full Electroporation-Mediated Gene Transfer Directly to the Swine Heart
title_fullStr Electroporation-Mediated Gene Transfer Directly to the Swine Heart
title_full_unstemmed Electroporation-Mediated Gene Transfer Directly to the Swine Heart
title_short Electroporation-Mediated Gene Transfer Directly to the Swine Heart
title_sort electroporation-mediated gene transfer directly to the swine heart
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3387511/
https://www.ncbi.nlm.nih.gov/pubmed/22456328
http://dx.doi.org/10.1038/gt.2012.15
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