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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2012
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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. |
format | Online Article Text |
id | pubmed-3387511 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
record_format | MEDLINE/PubMed |
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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