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Mapping of bionic array electric field focusing in plasmid DNA-based gene electrotransfer
Molecular medicine through gene therapy is challenged to achieve targeted action. This is now possible utilizing bionic electrode arrays for focal delivery of naked (plasmid) DNA via gene electrotransfer. Here, we establish the properties of array-based electroporation affecting targeted gene delive...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4827009/ https://www.ncbi.nlm.nih.gov/pubmed/26826485 http://dx.doi.org/10.1038/gt.2016.8 |
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author | Browne, C J Pinyon, J L Housley, D M Crawford, E N Lovell, N H Klugmann, M Housley, G D |
author_facet | Browne, C J Pinyon, J L Housley, D M Crawford, E N Lovell, N H Klugmann, M Housley, G D |
author_sort | Browne, C J |
collection | PubMed |
description | Molecular medicine through gene therapy is challenged to achieve targeted action. This is now possible utilizing bionic electrode arrays for focal delivery of naked (plasmid) DNA via gene electrotransfer. Here, we establish the properties of array-based electroporation affecting targeted gene delivery. An array with eight 300 μm platinum ring electrodes configured as a cochlear implant bionic interface was used to transduce HEK293 cell monolayers with a plasmid-DNA green fluorescent protein (GFP) reporter gene construct. Electroporation parameters were pulse intensity, number, duration, separation and electrode configuration. The latter determined the shape of the electric fields, which were mapped using a voltage probe. Electrode array-based electroporation was found to require ~100 × lower applied voltages for cell transduction than conventional electroporation. This was found to be due to compression of the field lines orthogonal to the array. A circular area of GFP-positive cells was created when the electrodes were ganged together as four adjacent anodes and four cathodes, whereas alternating electrode polarity created a linear area of GFP-positive cells. The refinement of gene delivery parameters was validated in vivo in the guinea pig cochlea. These findings have significant clinical ramifications, where spatiotemporal control of gene expression can be predicted by manipulation of the electric field via current steering at a cellular level. |
format | Online Article Text |
id | pubmed-4827009 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48270092016-04-22 Mapping of bionic array electric field focusing in plasmid DNA-based gene electrotransfer Browne, C J Pinyon, J L Housley, D M Crawford, E N Lovell, N H Klugmann, M Housley, G D Gene Ther Original Article – Enabling Technologies Molecular medicine through gene therapy is challenged to achieve targeted action. This is now possible utilizing bionic electrode arrays for focal delivery of naked (plasmid) DNA via gene electrotransfer. Here, we establish the properties of array-based electroporation affecting targeted gene delivery. An array with eight 300 μm platinum ring electrodes configured as a cochlear implant bionic interface was used to transduce HEK293 cell monolayers with a plasmid-DNA green fluorescent protein (GFP) reporter gene construct. Electroporation parameters were pulse intensity, number, duration, separation and electrode configuration. The latter determined the shape of the electric fields, which were mapped using a voltage probe. Electrode array-based electroporation was found to require ~100 × lower applied voltages for cell transduction than conventional electroporation. This was found to be due to compression of the field lines orthogonal to the array. A circular area of GFP-positive cells was created when the electrodes were ganged together as four adjacent anodes and four cathodes, whereas alternating electrode polarity created a linear area of GFP-positive cells. The refinement of gene delivery parameters was validated in vivo in the guinea pig cochlea. These findings have significant clinical ramifications, where spatiotemporal control of gene expression can be predicted by manipulation of the electric field via current steering at a cellular level. Nature Publishing Group 2016-04 2016-02-25 /pmc/articles/PMC4827009/ /pubmed/26826485 http://dx.doi.org/10.1038/gt.2016.8 Text en Copyright © 2016 Macmillan Publishers Limited http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/ |
spellingShingle | Original Article – Enabling Technologies Browne, C J Pinyon, J L Housley, D M Crawford, E N Lovell, N H Klugmann, M Housley, G D Mapping of bionic array electric field focusing in plasmid DNA-based gene electrotransfer |
title | Mapping of bionic array electric field focusing in plasmid DNA-based gene electrotransfer |
title_full | Mapping of bionic array electric field focusing in plasmid DNA-based gene electrotransfer |
title_fullStr | Mapping of bionic array electric field focusing in plasmid DNA-based gene electrotransfer |
title_full_unstemmed | Mapping of bionic array electric field focusing in plasmid DNA-based gene electrotransfer |
title_short | Mapping of bionic array electric field focusing in plasmid DNA-based gene electrotransfer |
title_sort | mapping of bionic array electric field focusing in plasmid dna-based gene electrotransfer |
topic | Original Article – Enabling Technologies |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4827009/ https://www.ncbi.nlm.nih.gov/pubmed/26826485 http://dx.doi.org/10.1038/gt.2016.8 |
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