Cited by 62Retinal Development and DisordersNeurogenesis and neuroplasticity mechanismsZebrafish Biomedical Research Applications

Fgf signaling is required for photoreceptor maintenance in the adult zebrafish retina

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Hochmann, Sarah, Kaslin, Jan, Hans, Stefan, Weber, Anke, Machate, Anja, Geffarth, Michaela, Funk, Richard H. W., Brand, Michael·2012·PLoS ONE

Abstract

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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References 63 · Cited by 62

Authors
Hochmann, S., Kaslin, J., Hans, S., Weber, A., Machate, A., Geffarth, M., Funk, R. H. W., & Brand, M.
Affiliations
  • Center for Regenerative Therapies Dresden (DE)
  • Technische Universität Dresden (DE)
Corresponding author
Brand, Michael
Venue
PLoS ONE
Published
2012-01-26
Volume
7
Issue
1
Pages
e30365
ISSN
1932-6203 (ISSN-L)
OpenAlex
W1987520439
Cited by
62
References
63
Citations by year
2026: 3 · 2025: 1 · 2024: 3 · 2023: 1 · 2022: 5 · 2021: 6 · 2020: 9 · 2019: 4 · 2018: 4 · 2017: 4 · 2016: 4 · 2015: 1 · 2014: 6 · 2013: 8 · 2012: 3
FWCI
2.32
Type
journal article
Language
en
Open access
Locations
  • PLoS ONE (publishedVersion, cc-by)
  • Europe PMC (PubMed Central) (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • Monash University Research Portal (Monash University) (submittedVersion, cc-by)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
  • Figshare (submittedVersion, cc-by)
Funders
  • European Commission
  • Deutsche Forschungsgemeinschaft (SFB 655)
  • Zentrum für Regenerative Therapien Dresden
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Retinal Development and Disorders
  • Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Zebrafish Biomedical Research Applications
Keywords
FGF signaling, photoreceptor degeneration, retinal regeneration, zebrafish retina, FGF receptor 1, dominant negative receptor, rod and cone photoreceptors, adult retina
MeSH terms
Age Factors, Animals, Cell Survival, Fibroblast Growth Factors, Retina, Zebrafish, Signal Transduction, Cell Death, Receptors, Fibroblast Growth Factor, Gene Expression Regulation, Developmental, Photoreceptor Cells, Vertebrate, Animals, Genetically Modified, Receptor, Fibroblast Growth Factor, Type 1

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