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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...
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/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. |
format | Online Article Text |
id | pubmed-5014459 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
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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