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Topical Use of Angiopoietin-like Protein 2 RNAi-loaded Lipid Nanoparticles Suppresses Corneal Neovascularization

Corneal neovascularization (CNV) is a sight-threatening condition that is encountered in various inflammatory settings including chemical injury. We recently confirmed that angiopoietin-like protein 2 (ANGPTL2) is a potent angiogenic and proinflammatory factor in the cornea, and we have produced a s...

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Autores principales: Taketani, Yukako, Usui, Tomohiko, Toyono, Tetsuya, Shima, Nobuyuki, Yokoo, Seiichi, Kimakura, Mikiko, Yamagami, Satoru, Ohno, Shinichiro, Onodera, Risako, Tahara, Kohei, Takeuchi, Hirofumi, Kuroda, Masahiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5014459/
https://www.ncbi.nlm.nih.gov/pubmed/27111418
http://dx.doi.org/10.1038/mtna.2016.1
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author Taketani, Yukako
Usui, Tomohiko
Toyono, Tetsuya
Shima, Nobuyuki
Yokoo, Seiichi
Kimakura, Mikiko
Yamagami, Satoru
Ohno, Shinichiro
Onodera, Risako
Tahara, Kohei
Takeuchi, Hirofumi
Kuroda, Masahiko
author_facet Taketani, Yukako
Usui, Tomohiko
Toyono, Tetsuya
Shima, Nobuyuki
Yokoo, Seiichi
Kimakura, Mikiko
Yamagami, Satoru
Ohno, Shinichiro
Onodera, Risako
Tahara, Kohei
Takeuchi, Hirofumi
Kuroda, Masahiko
author_sort Taketani, Yukako
collection PubMed
description Corneal neovascularization (CNV) is a sight-threatening condition that is encountered in various inflammatory settings including chemical injury. We recently confirmed that angiopoietin-like protein 2 (ANGPTL2) is a potent angiogenic and proinflammatory factor in the cornea, and we have produced a single-stranded proline-modified short hairpin anti-ANGPTL2 RNA interference molecule that is carried in a lipid nanoparticle (ANGPTL2 Li-pshRNA) for topical application. In this study, we have further examined the topical delivery and anti-ANGPTL2 activity of this molecule and have found that fluorescence-labeled ANGPTL2 Li-pshRNA eye drops can penetrate all layers of the cornea and that ANGPTL2 mRNA expression was dramatically inhibited in both epithelium and stroma at 12 and 24 hours after administration. We also examined the inhibitory effect of ANGPTL2 Li-pshRNA on CNV in a mouse chemical injury model and found that the area of angiogenesis was significantly decreased in corneas treated with ANGPTL2 Li-pshRNA eye drops compared to controls. Together, these findings indicate that this modified RNA interference agent is clinically viable in a topical formulation for use against CNV.
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spelling pubmed-50144592016-09-19 Topical Use of Angiopoietin-like Protein 2 RNAi-loaded Lipid Nanoparticles Suppresses Corneal Neovascularization Taketani, Yukako Usui, Tomohiko Toyono, Tetsuya Shima, Nobuyuki Yokoo, Seiichi Kimakura, Mikiko Yamagami, Satoru Ohno, Shinichiro Onodera, Risako Tahara, Kohei Takeuchi, Hirofumi Kuroda, Masahiko Mol Ther Nucleic Acids Original Article Corneal neovascularization (CNV) is a sight-threatening condition that is encountered in various inflammatory settings including chemical injury. We recently confirmed that angiopoietin-like protein 2 (ANGPTL2) is a potent angiogenic and proinflammatory factor in the cornea, and we have produced a single-stranded proline-modified short hairpin anti-ANGPTL2 RNA interference molecule that is carried in a lipid nanoparticle (ANGPTL2 Li-pshRNA) for topical application. In this study, we have further examined the topical delivery and anti-ANGPTL2 activity of this molecule and have found that fluorescence-labeled ANGPTL2 Li-pshRNA eye drops can penetrate all layers of the cornea and that ANGPTL2 mRNA expression was dramatically inhibited in both epithelium and stroma at 12 and 24 hours after administration. We also examined the inhibitory effect of ANGPTL2 Li-pshRNA on CNV in a mouse chemical injury model and found that the area of angiogenesis was significantly decreased in corneas treated with ANGPTL2 Li-pshRNA eye drops compared to controls. Together, these findings indicate that this modified RNA interference agent is clinically viable in a topical formulation for use against CNV. Nature Publishing Group 2016-03 2016-03-08 /pmc/articles/PMC5014459/ /pubmed/27111418 http://dx.doi.org/10.1038/mtna.2016.1 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
Taketani, Yukako
Usui, Tomohiko
Toyono, Tetsuya
Shima, Nobuyuki
Yokoo, Seiichi
Kimakura, Mikiko
Yamagami, Satoru
Ohno, Shinichiro
Onodera, Risako
Tahara, Kohei
Takeuchi, Hirofumi
Kuroda, Masahiko
Topical Use of Angiopoietin-like Protein 2 RNAi-loaded Lipid Nanoparticles Suppresses Corneal Neovascularization
title Topical Use of Angiopoietin-like Protein 2 RNAi-loaded Lipid Nanoparticles Suppresses Corneal Neovascularization
title_full Topical Use of Angiopoietin-like Protein 2 RNAi-loaded Lipid Nanoparticles Suppresses Corneal Neovascularization
title_fullStr Topical Use of Angiopoietin-like Protein 2 RNAi-loaded Lipid Nanoparticles Suppresses Corneal Neovascularization
title_full_unstemmed Topical Use of Angiopoietin-like Protein 2 RNAi-loaded Lipid Nanoparticles Suppresses Corneal Neovascularization
title_short Topical Use of Angiopoietin-like Protein 2 RNAi-loaded Lipid Nanoparticles Suppresses Corneal Neovascularization
title_sort topical use of angiopoietin-like protein 2 rnai-loaded lipid nanoparticles suppresses corneal neovascularization
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5014459/
https://www.ncbi.nlm.nih.gov/pubmed/27111418
http://dx.doi.org/10.1038/mtna.2016.1
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