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Kidney-specific Sonoporation-mediated Gene Transfer
Sonoporation can deliver agents to target local organs by systemic administration, while decreasing the associated risk of adverse effects. Sonoporation has been used for a variety of materials and in a variety of organs. Herein, we demonstrated that local sonoporation to the kidney can offer highly...
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/PMC4754547/ https://www.ncbi.nlm.nih.gov/pubmed/26419704 http://dx.doi.org/10.1038/mt.2015.171 |
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author | Ishida, Ryo Kami, Daisuke Kusaba, Tetsuro Kirita, Yuhei Kishida, Tsunao Mazda, Osam Adachi, Takaomi Gojo, Satoshi |
author_facet | Ishida, Ryo Kami, Daisuke Kusaba, Tetsuro Kirita, Yuhei Kishida, Tsunao Mazda, Osam Adachi, Takaomi Gojo, Satoshi |
author_sort | Ishida, Ryo |
collection | PubMed |
description | Sonoporation can deliver agents to target local organs by systemic administration, while decreasing the associated risk of adverse effects. Sonoporation has been used for a variety of materials and in a variety of organs. Herein, we demonstrated that local sonoporation to the kidney can offer highly efficient transfer of oligonucleotides, which were systemically administrated to the tubular epithelium with high specificity. Ultrasonic wave irradiation to the kidney collapsed the microbubbles and transiently affected the glomerular filtration barrier and increased glomerular permeability. Oligonucleotides were passed through the barrier all at once and were absorbed throughout the tubular epithelium. Tumor necrosis factor alpha (TNFα), which plays a central role in renal ischemia–reperfusion injury, was targeted using small interfering RNA (siRNA) with renal sonoporation in a murine model. The reduction of TNFα expression after single gene transfer significantly inhibited the expression of kidney injury markers, suggesting that systemic administration of siRNA under temporary and local sonoporation could be applicable in the clinical setting of ischemic acute kidney injury. |
format | Online Article Text |
id | pubmed-4754547 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47545472016-03-03 Kidney-specific Sonoporation-mediated Gene Transfer Ishida, Ryo Kami, Daisuke Kusaba, Tetsuro Kirita, Yuhei Kishida, Tsunao Mazda, Osam Adachi, Takaomi Gojo, Satoshi Mol Ther Original Article Sonoporation can deliver agents to target local organs by systemic administration, while decreasing the associated risk of adverse effects. Sonoporation has been used for a variety of materials and in a variety of organs. Herein, we demonstrated that local sonoporation to the kidney can offer highly efficient transfer of oligonucleotides, which were systemically administrated to the tubular epithelium with high specificity. Ultrasonic wave irradiation to the kidney collapsed the microbubbles and transiently affected the glomerular filtration barrier and increased glomerular permeability. Oligonucleotides were passed through the barrier all at once and were absorbed throughout the tubular epithelium. Tumor necrosis factor alpha (TNFα), which plays a central role in renal ischemia–reperfusion injury, was targeted using small interfering RNA (siRNA) with renal sonoporation in a murine model. The reduction of TNFα expression after single gene transfer significantly inhibited the expression of kidney injury markers, suggesting that systemic administration of siRNA under temporary and local sonoporation could be applicable in the clinical setting of ischemic acute kidney injury. Nature Publishing Group 2016-02 2015-10-27 /pmc/articles/PMC4754547/ /pubmed/26419704 http://dx.doi.org/10.1038/mt.2015.171 Text en Copyright © 2016 Official journal of the American Society of Gene & Cell Therapy 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 Ishida, Ryo Kami, Daisuke Kusaba, Tetsuro Kirita, Yuhei Kishida, Tsunao Mazda, Osam Adachi, Takaomi Gojo, Satoshi Kidney-specific Sonoporation-mediated Gene Transfer |
title | Kidney-specific Sonoporation-mediated Gene Transfer |
title_full | Kidney-specific Sonoporation-mediated Gene Transfer |
title_fullStr | Kidney-specific Sonoporation-mediated Gene Transfer |
title_full_unstemmed | Kidney-specific Sonoporation-mediated Gene Transfer |
title_short | Kidney-specific Sonoporation-mediated Gene Transfer |
title_sort | kidney-specific sonoporation-mediated gene transfer |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4754547/ https://www.ncbi.nlm.nih.gov/pubmed/26419704 http://dx.doi.org/10.1038/mt.2015.171 |
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