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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...

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Autores principales: Hochmann, Sarah, Kaslin, Jan, Hans, Stefan, Weber, Anke, Machate, Anja, Geffarth, Michaela, Funk, Richard H. W., Brand, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
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.
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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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