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Fgf Signaling is Required for Photoreceptor Maintenance in the Adult Zebrafish Retina
Fibroblast growth factors (Fgf) are secreted signaling molecules that have mitogenic, patterning, neurotrophic and angiogenic properties. Their importance during embryonic development in patterning and morphogenesis of the vertebrate eye is well known, but less is known about the role of Fgfs in the...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3266925/ https://www.ncbi.nlm.nih.gov/pubmed/22291943 http://dx.doi.org/10.1371/journal.pone.0030365 |
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author | Hochmann, Sarah Kaslin, Jan Hans, Stefan Weber, Anke Machate, Anja Geffarth, Michaela Funk, Richard H. W. Brand, Michael |
author_facet | Hochmann, Sarah Kaslin, Jan Hans, Stefan Weber, Anke Machate, Anja Geffarth, Michaela Funk, Richard H. W. Brand, Michael |
author_sort | Hochmann, Sarah |
collection | PubMed |
description | Fibroblast growth factors (Fgf) are secreted signaling molecules that have mitogenic, patterning, neurotrophic and angiogenic properties. Their importance during embryonic development in patterning and morphogenesis of the vertebrate eye is well known, but less is known about the role of Fgfs in the adult vertebrate retina. To address Fgf function in adult retina, we determined the spatial distribution of components of the Fgf signaling pathway in the adult zebrafish retina. We detected differential expression of Fgf receptors, ligands and downstream Fgf targets within specific retinal layers. Furthermore, we blocked Fgf signaling in the retina, by expressing a dominant negative variant of Fgf receptor 1 conditionally in transgenic animals. After blocking Fgf signaling we observe a fast and progressive photoreceptor degeneration and disorganization of retinal tissue, coupled with cell death in the outer nuclear layer. Following the degeneration of photoreceptors, a profound regeneration response is triggered that starts with proliferation in the inner nuclear layer. Ultimately, rod and cone photoreceptors are regenerated completely. Our study reveals the requirement of Fgf signaling to maintain photoreceptors and for proliferation during regeneration in the adult zebrafish retina. |
format | Online Article Text |
id | pubmed-3266925 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-32669252012-01-30 Fgf Signaling is Required for Photoreceptor Maintenance in the Adult Zebrafish Retina Hochmann, Sarah Kaslin, Jan Hans, Stefan Weber, Anke Machate, Anja Geffarth, Michaela Funk, Richard H. W. Brand, Michael PLoS One Research Article Fibroblast growth factors (Fgf) are secreted signaling molecules that have mitogenic, patterning, neurotrophic and angiogenic properties. Their importance during embryonic development in patterning and morphogenesis of the vertebrate eye is well known, but less is known about the role of Fgfs in the adult vertebrate retina. To address Fgf function in adult retina, we determined the spatial distribution of components of the Fgf signaling pathway in the adult zebrafish retina. We detected differential expression of Fgf receptors, ligands and downstream Fgf targets within specific retinal layers. Furthermore, we blocked Fgf signaling in the retina, by expressing a dominant negative variant of Fgf receptor 1 conditionally in transgenic animals. After blocking Fgf signaling we observe a fast and progressive photoreceptor degeneration and disorganization of retinal tissue, coupled with cell death in the outer nuclear layer. Following the degeneration of photoreceptors, a profound regeneration response is triggered that starts with proliferation in the inner nuclear layer. Ultimately, rod and cone photoreceptors are regenerated completely. Our study reveals the requirement of Fgf signaling to maintain photoreceptors and for proliferation during regeneration in the adult zebrafish retina. Public Library of Science 2012-01-26 /pmc/articles/PMC3266925/ /pubmed/22291943 http://dx.doi.org/10.1371/journal.pone.0030365 Text en Hochmann 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Hochmann, Sarah Kaslin, Jan Hans, Stefan Weber, Anke Machate, Anja Geffarth, Michaela Funk, Richard H. W. Brand, Michael Fgf Signaling is Required for Photoreceptor Maintenance in the Adult Zebrafish Retina |
title | Fgf Signaling is Required for Photoreceptor Maintenance in the Adult Zebrafish Retina |
title_full | Fgf Signaling is Required for Photoreceptor Maintenance in the Adult Zebrafish Retina |
title_fullStr | Fgf Signaling is Required for Photoreceptor Maintenance in the Adult Zebrafish Retina |
title_full_unstemmed | Fgf Signaling is Required for Photoreceptor Maintenance in the Adult Zebrafish Retina |
title_short | Fgf Signaling is Required for Photoreceptor Maintenance in the Adult Zebrafish Retina |
title_sort | fgf signaling is required for photoreceptor maintenance in the adult zebrafish retina |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3266925/ https://www.ncbi.nlm.nih.gov/pubmed/22291943 http://dx.doi.org/10.1371/journal.pone.0030365 |
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