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Efficacy and Safety of Pancreas-Targeted Hydrodynamic Gene Delivery in Rats
Development of an effective, safe, and convenient method for gene delivery to the pancreas is a critical step toward gene therapy for pancreatic diseases. Therefore, we tested the possibility of applying the principle of hydrodynamic gene delivery for successful gene transfer to pancreas using rats...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Gene & Cell Therapy
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5612811/ https://www.ncbi.nlm.nih.gov/pubmed/29246326 http://dx.doi.org/10.1016/j.omtn.2017.08.009 |
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author | Ogawa, Kohei Kamimura, Kenya Kobayashi, Yuji Abe, Hiroyuki Yokoo, Takeshi Sakai, Norihiro Nagoya, Takuro Sakamaki, Akira Abe, Satoshi Hayashi, Kazunao Ikarashi, Satoshi Kohisa, Junji Tsuchida, Masanori Aoyagi, Yutaka Zhang, Guisheng Liu, Dexi Terai, Shuji |
author_facet | Ogawa, Kohei Kamimura, Kenya Kobayashi, Yuji Abe, Hiroyuki Yokoo, Takeshi Sakai, Norihiro Nagoya, Takuro Sakamaki, Akira Abe, Satoshi Hayashi, Kazunao Ikarashi, Satoshi Kohisa, Junji Tsuchida, Masanori Aoyagi, Yutaka Zhang, Guisheng Liu, Dexi Terai, Shuji |
author_sort | Ogawa, Kohei |
collection | PubMed |
description | Development of an effective, safe, and convenient method for gene delivery to the pancreas is a critical step toward gene therapy for pancreatic diseases. Therefore, we tested the possibility of applying the principle of hydrodynamic gene delivery for successful gene transfer to pancreas using rats as a model. The established procedure involves the insertion of a catheter into the superior mesenteric vein with temporary blood flow occlusion at the portal vein and hydrodynamic injection of DNA solution. We demonstrated that our procedure achieved efficient pancreas-specific gene expression that was 2,000-fold higher than that seen in the pancreas after the systemic hydrodynamic gene delivery. In addition, the level of gene expression achieved in the pancreas by the pancreas-specific gene delivery was comparable to the level in the liver achieved by a liver-specific hydrodynamic gene delivery. The optimal level of reporter gene expression in the pancreas requires an injection volume equivalent to 2.0% body weight with flow rate of 1 mL/s and plasmid DNA concentration at 5 μg/mL. With the exception of transient expansion of intercellular spaces and elevation of serum amylase levels, which recovered within 3 days, no permanent tissue damage was observed. These results suggest that pancreas-targeted hydrodynamic gene delivery is an effective and safe method for gene delivery to the pancreas and clinically applicable. |
format | Online Article Text |
id | pubmed-5612811 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | American Society of Gene & Cell Therapy |
record_format | MEDLINE/PubMed |
spelling | pubmed-56128112017-10-02 Efficacy and Safety of Pancreas-Targeted Hydrodynamic Gene Delivery in Rats Ogawa, Kohei Kamimura, Kenya Kobayashi, Yuji Abe, Hiroyuki Yokoo, Takeshi Sakai, Norihiro Nagoya, Takuro Sakamaki, Akira Abe, Satoshi Hayashi, Kazunao Ikarashi, Satoshi Kohisa, Junji Tsuchida, Masanori Aoyagi, Yutaka Zhang, Guisheng Liu, Dexi Terai, Shuji Mol Ther Nucleic Acids Original Article Development of an effective, safe, and convenient method for gene delivery to the pancreas is a critical step toward gene therapy for pancreatic diseases. Therefore, we tested the possibility of applying the principle of hydrodynamic gene delivery for successful gene transfer to pancreas using rats as a model. The established procedure involves the insertion of a catheter into the superior mesenteric vein with temporary blood flow occlusion at the portal vein and hydrodynamic injection of DNA solution. We demonstrated that our procedure achieved efficient pancreas-specific gene expression that was 2,000-fold higher than that seen in the pancreas after the systemic hydrodynamic gene delivery. In addition, the level of gene expression achieved in the pancreas by the pancreas-specific gene delivery was comparable to the level in the liver achieved by a liver-specific hydrodynamic gene delivery. The optimal level of reporter gene expression in the pancreas requires an injection volume equivalent to 2.0% body weight with flow rate of 1 mL/s and plasmid DNA concentration at 5 μg/mL. With the exception of transient expansion of intercellular spaces and elevation of serum amylase levels, which recovered within 3 days, no permanent tissue damage was observed. These results suggest that pancreas-targeted hydrodynamic gene delivery is an effective and safe method for gene delivery to the pancreas and clinically applicable. American Society of Gene & Cell Therapy 2017-08-18 /pmc/articles/PMC5612811/ /pubmed/29246326 http://dx.doi.org/10.1016/j.omtn.2017.08.009 Text en © 2017 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Ogawa, Kohei Kamimura, Kenya Kobayashi, Yuji Abe, Hiroyuki Yokoo, Takeshi Sakai, Norihiro Nagoya, Takuro Sakamaki, Akira Abe, Satoshi Hayashi, Kazunao Ikarashi, Satoshi Kohisa, Junji Tsuchida, Masanori Aoyagi, Yutaka Zhang, Guisheng Liu, Dexi Terai, Shuji Efficacy and Safety of Pancreas-Targeted Hydrodynamic Gene Delivery in Rats |
title | Efficacy and Safety of Pancreas-Targeted Hydrodynamic Gene Delivery in Rats |
title_full | Efficacy and Safety of Pancreas-Targeted Hydrodynamic Gene Delivery in Rats |
title_fullStr | Efficacy and Safety of Pancreas-Targeted Hydrodynamic Gene Delivery in Rats |
title_full_unstemmed | Efficacy and Safety of Pancreas-Targeted Hydrodynamic Gene Delivery in Rats |
title_short | Efficacy and Safety of Pancreas-Targeted Hydrodynamic Gene Delivery in Rats |
title_sort | efficacy and safety of pancreas-targeted hydrodynamic gene delivery in rats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5612811/ https://www.ncbi.nlm.nih.gov/pubmed/29246326 http://dx.doi.org/10.1016/j.omtn.2017.08.009 |
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