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Melanosomes in pigmented epithelia maintain eye lens transparency during zebrafish embryonic development
Altered levels of trace elements are associated with increased oxidative stress that is eventually responsible for pathologic conditions. Oxidative stress has been proposed to be involved in eye diseases, including cataract formation. We visualized the distribution of metals and other trace elements...
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/PMC4855227/ https://www.ncbi.nlm.nih.gov/pubmed/27141993 http://dx.doi.org/10.1038/srep25046 |
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author | Takamiya, Masanari Xu, Feng Suhonen, Heikki Gourain, Victor Yang, Lixin Ho, Nga Yu Helfen, Lukas Schröck, Anne Etard, Christelle Grabher, Clemens Rastegar, Sepand Schlunck, Günther Reinhard, Thomas Baumbach, Tilo Strähle, Uwe |
author_facet | Takamiya, Masanari Xu, Feng Suhonen, Heikki Gourain, Victor Yang, Lixin Ho, Nga Yu Helfen, Lukas Schröck, Anne Etard, Christelle Grabher, Clemens Rastegar, Sepand Schlunck, Günther Reinhard, Thomas Baumbach, Tilo Strähle, Uwe |
author_sort | Takamiya, Masanari |
collection | PubMed |
description | Altered levels of trace elements are associated with increased oxidative stress that is eventually responsible for pathologic conditions. Oxidative stress has been proposed to be involved in eye diseases, including cataract formation. We visualized the distribution of metals and other trace elements in the eye of zebrafish embryos by micro X-ray fluorescence (μ-XRF) imaging. Many elements showed highest accumulation in the retinal pigment epithelium (RPE) of the zebrafish embryo. Knockdown of the zebrafish brown locus homologues tyrp1a/b eliminated accumulation of these elements in the RPE, indicating that they are bound by mature melanosomes. Furthermore, albino (slc45a2) mutants, which completely lack melanosomes, developed abnormal lens reflections similar to the congenital cataract caused by mutation of the myosin chaperon Unc45b, and an in situ spin trapping assay revealed increased oxidative stress in the lens of albino mutants. Finally transplanting a wildtype lens into an albino mutant background resulted in cataract formation. These data suggest that melanosomes in pigment epithelial cells protect the lens from oxidative stress during embryonic development, likely by buffering trace elements. |
format | Online Article Text |
id | pubmed-4855227 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48552272016-05-18 Melanosomes in pigmented epithelia maintain eye lens transparency during zebrafish embryonic development Takamiya, Masanari Xu, Feng Suhonen, Heikki Gourain, Victor Yang, Lixin Ho, Nga Yu Helfen, Lukas Schröck, Anne Etard, Christelle Grabher, Clemens Rastegar, Sepand Schlunck, Günther Reinhard, Thomas Baumbach, Tilo Strähle, Uwe Sci Rep Article Altered levels of trace elements are associated with increased oxidative stress that is eventually responsible for pathologic conditions. Oxidative stress has been proposed to be involved in eye diseases, including cataract formation. We visualized the distribution of metals and other trace elements in the eye of zebrafish embryos by micro X-ray fluorescence (μ-XRF) imaging. Many elements showed highest accumulation in the retinal pigment epithelium (RPE) of the zebrafish embryo. Knockdown of the zebrafish brown locus homologues tyrp1a/b eliminated accumulation of these elements in the RPE, indicating that they are bound by mature melanosomes. Furthermore, albino (slc45a2) mutants, which completely lack melanosomes, developed abnormal lens reflections similar to the congenital cataract caused by mutation of the myosin chaperon Unc45b, and an in situ spin trapping assay revealed increased oxidative stress in the lens of albino mutants. Finally transplanting a wildtype lens into an albino mutant background resulted in cataract formation. These data suggest that melanosomes in pigment epithelial cells protect the lens from oxidative stress during embryonic development, likely by buffering trace elements. Nature Publishing Group 2016-05-04 /pmc/articles/PMC4855227/ /pubmed/27141993 http://dx.doi.org/10.1038/srep25046 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 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/4.0/ |
spellingShingle | Article Takamiya, Masanari Xu, Feng Suhonen, Heikki Gourain, Victor Yang, Lixin Ho, Nga Yu Helfen, Lukas Schröck, Anne Etard, Christelle Grabher, Clemens Rastegar, Sepand Schlunck, Günther Reinhard, Thomas Baumbach, Tilo Strähle, Uwe Melanosomes in pigmented epithelia maintain eye lens transparency during zebrafish embryonic development |
title | Melanosomes in pigmented epithelia maintain eye lens transparency during zebrafish embryonic development |
title_full | Melanosomes in pigmented epithelia maintain eye lens transparency during zebrafish embryonic development |
title_fullStr | Melanosomes in pigmented epithelia maintain eye lens transparency during zebrafish embryonic development |
title_full_unstemmed | Melanosomes in pigmented epithelia maintain eye lens transparency during zebrafish embryonic development |
title_short | Melanosomes in pigmented epithelia maintain eye lens transparency during zebrafish embryonic development |
title_sort | melanosomes in pigmented epithelia maintain eye lens transparency during zebrafish embryonic development |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4855227/ https://www.ncbi.nlm.nih.gov/pubmed/27141993 http://dx.doi.org/10.1038/srep25046 |
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