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Transient expression of Wnt5a elicits ocular features of pseudoexfoliation syndrome in mice
PURPOSE: Pseudoexfoliation (PEX) syndrome is an age-related systemic disease with ocular manifestations. The development of animal models is critical in order to elucidate the cause of the disease and to test potential treatment regimens. The purpose of this study is to report phenotypes found in mo...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6402630/ https://www.ncbi.nlm.nih.gov/pubmed/30840655 http://dx.doi.org/10.1371/journal.pone.0212569 |
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author | Yuan, Yong Schlötzer-Schrehardt, Ursula Ritch, Robert Call, Mindy Chu, Fred B. Dong, Fei Rice, Taylor Zhang, Jianhua Kao, Winston W.-Y. |
author_facet | Yuan, Yong Schlötzer-Schrehardt, Ursula Ritch, Robert Call, Mindy Chu, Fred B. Dong, Fei Rice, Taylor Zhang, Jianhua Kao, Winston W.-Y. |
author_sort | Yuan, Yong |
collection | PubMed |
description | PURPOSE: Pseudoexfoliation (PEX) syndrome is an age-related systemic disease with ocular manifestations. The development of animal models is critical in order to elucidate the cause of the disease and to test potential treatment regimens. The purpose of this study is to report phenotypes found in mouse eyes injected with Adenovirus coding Wnt5a. Some of the phenotypes resemble those found in PEX patients while others are different. METHODS: Recombinant Adenovirus coding Wnt5a or green fluorescent protein (GFP) were injected into mouse eyes. Two months after the injection, eyes were examined for PEX phenotypes using slit lamp, fluorescence stereomicroscope, histological staining, immunostaining and transmission electron microscope. RESULT: Certain ocular features of PEX syndrome were found in mouse eyes injected with recombinant Adenovirus coding Wnt5a. These features include accumulation of exfoliation-like extracellular material on surfaces of anterior segment structures and its dispersion in the anterior chamber, saw-tooth appearance and disrupted basement membrane of the posterior iris pigment epithelium, iris stromal atrophy and disorganized ciliary zonules. Ultrastructure analysis of the exfoliation material revealed that the microfibril structure found in this model was different from those of PEX patients. CONCLUSION: These features, resembling signs of ocular PEX syndrome in patients, suggest that new information obtained from this study will be helpful for developing better mouse models for PEX syndrome. |
format | Online Article Text |
id | pubmed-6402630 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-64026302019-03-17 Transient expression of Wnt5a elicits ocular features of pseudoexfoliation syndrome in mice Yuan, Yong Schlötzer-Schrehardt, Ursula Ritch, Robert Call, Mindy Chu, Fred B. Dong, Fei Rice, Taylor Zhang, Jianhua Kao, Winston W.-Y. PLoS One Research Article PURPOSE: Pseudoexfoliation (PEX) syndrome is an age-related systemic disease with ocular manifestations. The development of animal models is critical in order to elucidate the cause of the disease and to test potential treatment regimens. The purpose of this study is to report phenotypes found in mouse eyes injected with Adenovirus coding Wnt5a. Some of the phenotypes resemble those found in PEX patients while others are different. METHODS: Recombinant Adenovirus coding Wnt5a or green fluorescent protein (GFP) were injected into mouse eyes. Two months after the injection, eyes were examined for PEX phenotypes using slit lamp, fluorescence stereomicroscope, histological staining, immunostaining and transmission electron microscope. RESULT: Certain ocular features of PEX syndrome were found in mouse eyes injected with recombinant Adenovirus coding Wnt5a. These features include accumulation of exfoliation-like extracellular material on surfaces of anterior segment structures and its dispersion in the anterior chamber, saw-tooth appearance and disrupted basement membrane of the posterior iris pigment epithelium, iris stromal atrophy and disorganized ciliary zonules. Ultrastructure analysis of the exfoliation material revealed that the microfibril structure found in this model was different from those of PEX patients. CONCLUSION: These features, resembling signs of ocular PEX syndrome in patients, suggest that new information obtained from this study will be helpful for developing better mouse models for PEX syndrome. Public Library of Science 2019-03-06 /pmc/articles/PMC6402630/ /pubmed/30840655 http://dx.doi.org/10.1371/journal.pone.0212569 Text en © 2019 Yuan et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Yuan, Yong Schlötzer-Schrehardt, Ursula Ritch, Robert Call, Mindy Chu, Fred B. Dong, Fei Rice, Taylor Zhang, Jianhua Kao, Winston W.-Y. Transient expression of Wnt5a elicits ocular features of pseudoexfoliation syndrome in mice |
title | Transient expression of Wnt5a elicits ocular features of pseudoexfoliation syndrome in mice |
title_full | Transient expression of Wnt5a elicits ocular features of pseudoexfoliation syndrome in mice |
title_fullStr | Transient expression of Wnt5a elicits ocular features of pseudoexfoliation syndrome in mice |
title_full_unstemmed | Transient expression of Wnt5a elicits ocular features of pseudoexfoliation syndrome in mice |
title_short | Transient expression of Wnt5a elicits ocular features of pseudoexfoliation syndrome in mice |
title_sort | transient expression of wnt5a elicits ocular features of pseudoexfoliation syndrome in mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6402630/ https://www.ncbi.nlm.nih.gov/pubmed/30840655 http://dx.doi.org/10.1371/journal.pone.0212569 |
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