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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2017
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.
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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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