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Systemic delivery of miR-126 by miRNA-loaded Bubble liposomes for the treatment of hindlimb ischemia

Currently, micro RNA (miRNA) is considered an attractive target for therapeutic intervention. A significant obstacle to the miRNA-based treatments is the efficient delivery of miRNA to the target tissue. We have developed polyethylene glycol-modified liposomes (Bubble liposomes (BLs)) that entrap ul...

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Autores principales: Endo-Takahashi, Yoko, Negishi, Yoichi, Nakamura, Arisa, Ukai, Saori, Ooaku, Kotomi, Oda, Yusuke, Sugimoto, Katsutoshi, Moriyasu, Fuminori, Takagi, Norio, Suzuki, Ryo, Maruyama, Kazuo, Aramaki, Yukihiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3900923/
https://www.ncbi.nlm.nih.gov/pubmed/24457599
http://dx.doi.org/10.1038/srep03883
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author Endo-Takahashi, Yoko
Negishi, Yoichi
Nakamura, Arisa
Ukai, Saori
Ooaku, Kotomi
Oda, Yusuke
Sugimoto, Katsutoshi
Moriyasu, Fuminori
Takagi, Norio
Suzuki, Ryo
Maruyama, Kazuo
Aramaki, Yukihiko
author_facet Endo-Takahashi, Yoko
Negishi, Yoichi
Nakamura, Arisa
Ukai, Saori
Ooaku, Kotomi
Oda, Yusuke
Sugimoto, Katsutoshi
Moriyasu, Fuminori
Takagi, Norio
Suzuki, Ryo
Maruyama, Kazuo
Aramaki, Yukihiko
author_sort Endo-Takahashi, Yoko
collection PubMed
description Currently, micro RNA (miRNA) is considered an attractive target for therapeutic intervention. A significant obstacle to the miRNA-based treatments is the efficient delivery of miRNA to the target tissue. We have developed polyethylene glycol-modified liposomes (Bubble liposomes (BLs)) that entrap ultrasound (US) contrast gas and can serve as both plasmid DNA (pDNA) or small interfering RNA (siRNA) carriers and US contrast agents. In this study, we investigated the usability of miRNA-loaded BLs (mi-BLs) using a hindlimb ischemia model and miR-126. It has been reported that miR-126 promotes angiogenesis via the inhibition of negative regulators of VEGF signaling. We demonstrated that mi-BLs could be detected using diagnostic US and that mi-BLs with therapeutic US could deliver miR-126 to an ischemic hindlimb, leading to the induction of angiogenic factors and the improvement of blood flow. These results suggest that combining mi-BLs with US may be useful for US imaging and miRNA delivery.
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spelling pubmed-39009232014-01-24 Systemic delivery of miR-126 by miRNA-loaded Bubble liposomes for the treatment of hindlimb ischemia Endo-Takahashi, Yoko Negishi, Yoichi Nakamura, Arisa Ukai, Saori Ooaku, Kotomi Oda, Yusuke Sugimoto, Katsutoshi Moriyasu, Fuminori Takagi, Norio Suzuki, Ryo Maruyama, Kazuo Aramaki, Yukihiko Sci Rep Article Currently, micro RNA (miRNA) is considered an attractive target for therapeutic intervention. A significant obstacle to the miRNA-based treatments is the efficient delivery of miRNA to the target tissue. We have developed polyethylene glycol-modified liposomes (Bubble liposomes (BLs)) that entrap ultrasound (US) contrast gas and can serve as both plasmid DNA (pDNA) or small interfering RNA (siRNA) carriers and US contrast agents. In this study, we investigated the usability of miRNA-loaded BLs (mi-BLs) using a hindlimb ischemia model and miR-126. It has been reported that miR-126 promotes angiogenesis via the inhibition of negative regulators of VEGF signaling. We demonstrated that mi-BLs could be detected using diagnostic US and that mi-BLs with therapeutic US could deliver miR-126 to an ischemic hindlimb, leading to the induction of angiogenic factors and the improvement of blood flow. These results suggest that combining mi-BLs with US may be useful for US imaging and miRNA delivery. Nature Publishing Group 2014-01-24 /pmc/articles/PMC3900923/ /pubmed/24457599 http://dx.doi.org/10.1038/srep03883 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Article
Endo-Takahashi, Yoko
Negishi, Yoichi
Nakamura, Arisa
Ukai, Saori
Ooaku, Kotomi
Oda, Yusuke
Sugimoto, Katsutoshi
Moriyasu, Fuminori
Takagi, Norio
Suzuki, Ryo
Maruyama, Kazuo
Aramaki, Yukihiko
Systemic delivery of miR-126 by miRNA-loaded Bubble liposomes for the treatment of hindlimb ischemia
title Systemic delivery of miR-126 by miRNA-loaded Bubble liposomes for the treatment of hindlimb ischemia
title_full Systemic delivery of miR-126 by miRNA-loaded Bubble liposomes for the treatment of hindlimb ischemia
title_fullStr Systemic delivery of miR-126 by miRNA-loaded Bubble liposomes for the treatment of hindlimb ischemia
title_full_unstemmed Systemic delivery of miR-126 by miRNA-loaded Bubble liposomes for the treatment of hindlimb ischemia
title_short Systemic delivery of miR-126 by miRNA-loaded Bubble liposomes for the treatment of hindlimb ischemia
title_sort systemic delivery of mir-126 by mirna-loaded bubble liposomes for the treatment of hindlimb ischemia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3900923/
https://www.ncbi.nlm.nih.gov/pubmed/24457599
http://dx.doi.org/10.1038/srep03883
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