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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...

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Autores principales: Yuan, Yong, Schlötzer-Schrehardt, Ursula, Ritch, Robert, Call, Mindy, Chu, Fred B., Dong, Fei, Rice, Taylor, Zhang, Jianhua, Kao, Winston W.-Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
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.
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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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