Cargando…
Anti-angiogenic properties of microRNA-29a in preclinical ocular models
Abnormal neovascularization is an important cause of blindness in many ocular diseases, for which the etiology and pathogenic mechanisms remain incompletely understood. Recent studies have revealed the diverse roles of noncoding RNAs in various biological processes and facilitated the research and d...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9659377/ https://www.ncbi.nlm.nih.gov/pubmed/36322719 http://dx.doi.org/10.1073/pnas.2204795119 |
_version_ | 1784830184464056320 |
---|---|
author | Peng, De-Wei Lan, Chun-Lin Dong, Ling-Qin Jiang, Meng-Xi Xiao, Huan D’Amato, Robert J. Chi, Zai-Long |
author_facet | Peng, De-Wei Lan, Chun-Lin Dong, Ling-Qin Jiang, Meng-Xi Xiao, Huan D’Amato, Robert J. Chi, Zai-Long |
author_sort | Peng, De-Wei |
collection | PubMed |
description | Abnormal neovascularization is an important cause of blindness in many ocular diseases, for which the etiology and pathogenic mechanisms remain incompletely understood. Recent studies have revealed the diverse roles of noncoding RNAs in various biological processes and facilitated the research and development of the clinical application of numerous RNA drugs, including microRNAs. Here, we report the antiangiogenic activity of microRNA-29a (miR-29a) in three animal models of ocular neovascularization. The miR-29a knockout (KO) mice displayed enhanced vessel pruning, resulting in a decreased vascularized area during retinal development. In contrast, miR-29a deletion in adult mice accelerated angiogenesis in preclinical disease models, including corneal neovascularization, oxygen-induced retinopathy, and choroidal neovascularization, while the administration of agomir-29a ameliorated pathological neovascularization. Furthermore, miR-29a exerted inhibitory effects on endothelial cell proliferation, migration, and tube formation capacities. RNA sequencing analysis of retinas from miR-29a KO mice and RNA interference experiments identified platelet-derived growth factor C and several extracellular matrix genes as downstream targets of miR-29a involved in regulating ocular angiogenesis. Our data suggest that miR-29a may be a promising clinical candidate for the treatment of neovascular diseases. |
format | Online Article Text |
id | pubmed-9659377 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-96593772022-11-15 Anti-angiogenic properties of microRNA-29a in preclinical ocular models Peng, De-Wei Lan, Chun-Lin Dong, Ling-Qin Jiang, Meng-Xi Xiao, Huan D’Amato, Robert J. Chi, Zai-Long Proc Natl Acad Sci U S A Biological Sciences Abnormal neovascularization is an important cause of blindness in many ocular diseases, for which the etiology and pathogenic mechanisms remain incompletely understood. Recent studies have revealed the diverse roles of noncoding RNAs in various biological processes and facilitated the research and development of the clinical application of numerous RNA drugs, including microRNAs. Here, we report the antiangiogenic activity of microRNA-29a (miR-29a) in three animal models of ocular neovascularization. The miR-29a knockout (KO) mice displayed enhanced vessel pruning, resulting in a decreased vascularized area during retinal development. In contrast, miR-29a deletion in adult mice accelerated angiogenesis in preclinical disease models, including corneal neovascularization, oxygen-induced retinopathy, and choroidal neovascularization, while the administration of agomir-29a ameliorated pathological neovascularization. Furthermore, miR-29a exerted inhibitory effects on endothelial cell proliferation, migration, and tube formation capacities. RNA sequencing analysis of retinas from miR-29a KO mice and RNA interference experiments identified platelet-derived growth factor C and several extracellular matrix genes as downstream targets of miR-29a involved in regulating ocular angiogenesis. Our data suggest that miR-29a may be a promising clinical candidate for the treatment of neovascular diseases. National Academy of Sciences 2022-11-02 2022-11-08 /pmc/articles/PMC9659377/ /pubmed/36322719 http://dx.doi.org/10.1073/pnas.2204795119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Peng, De-Wei Lan, Chun-Lin Dong, Ling-Qin Jiang, Meng-Xi Xiao, Huan D’Amato, Robert J. Chi, Zai-Long Anti-angiogenic properties of microRNA-29a in preclinical ocular models |
title | Anti-angiogenic properties of microRNA-29a in preclinical ocular models |
title_full | Anti-angiogenic properties of microRNA-29a in preclinical ocular models |
title_fullStr | Anti-angiogenic properties of microRNA-29a in preclinical ocular models |
title_full_unstemmed | Anti-angiogenic properties of microRNA-29a in preclinical ocular models |
title_short | Anti-angiogenic properties of microRNA-29a in preclinical ocular models |
title_sort | anti-angiogenic properties of microrna-29a in preclinical ocular models |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9659377/ https://www.ncbi.nlm.nih.gov/pubmed/36322719 http://dx.doi.org/10.1073/pnas.2204795119 |
work_keys_str_mv | AT pengdewei antiangiogenicpropertiesofmicrorna29ainpreclinicalocularmodels AT lanchunlin antiangiogenicpropertiesofmicrorna29ainpreclinicalocularmodels AT donglingqin antiangiogenicpropertiesofmicrorna29ainpreclinicalocularmodels AT jiangmengxi antiangiogenicpropertiesofmicrorna29ainpreclinicalocularmodels AT xiaohuan antiangiogenicpropertiesofmicrorna29ainpreclinicalocularmodels AT damatorobertj antiangiogenicpropertiesofmicrorna29ainpreclinicalocularmodels AT chizailong antiangiogenicpropertiesofmicrorna29ainpreclinicalocularmodels |