PUBLICATION

Denervation impairs regeneration of amputated zebrafish fins

Authors
Simões, M.G., Bensimon-Brito, A., Fonseca, M., Farinho, A., Valério, F., Sousa, S., Kumar, A., Jacinto, A.
ID
ZDB-PUB-150101-1
Date
2014
Source
BMC Developmental Biology   14: 780 (Journal)
Registered Authors
Bensimon-Brito, Anabela
Keywords
none
MeSH Terms
  • Denervation
  • Gene Expression
  • Female
  • Zebrafish
  • Proliferating Cell Nuclear Antigen/metabolism
  • Animal Fins/innervation
  • Animal Fins/physiology*
  • Regeneration*
  • Mesoderm/cytology
  • Animals
  • Cell Proliferation
  • Zebrafish Proteins/genetics
  • Zebrafish Proteins/metabolism
(all 13)
PubMed
25551555 Full text @ BMC Dev. Biol.
Abstract
BackgroundZebrafish are able to regenerate many of its tissues and organs after damage. In amphibians this process is regulated by nerve fibres present at the site of injury, which have been proposed to release factors into the amputated limbs/fins, promoting and sustaining the proliferation of blastemal cells. Although some candidate factors have been proposed to mediate the nerve dependency of regeneration, the molecular mechanisms involved in this process remain unclear.ResultsWe have used zebrafish as a model system to address the role of nerve fibres in fin regeneration. We have developed a protocol for pectoral fin denervation followed by amputation and analysed the regenerative process under this experimental conditions. Upon denervation fins were able to close the wound and form a wound epidermis, but could not establish a functional apical epithelial cap, with a posterior failure of blastema formation and outgrowth, and the accumulation of several defects. The expression patterns of genes known to be key players during fin regeneration were altered upon denervation, suggesting that nerves can contribute to the regulation of the Fgf, Wnt and Shh pathways during zebrafish fin regeneration.ConclusionsOur results demonstrate that proper innervation of the zebrafish pectoral fin is essential for a successful regenerative process, and establish this organism as a useful model to understand the molecular and cellular mechanisms of nerve dependence, during vertebrate regeneration.
Genes / Markers
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Expression
Phenotype
No data available
Mutations / Transgenics
Allele Construct Type Affected Genomic Region
hu4008TgTransgenic Insertion
    zf131TgTransgenic Insertion
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      Human Disease / Model
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      Sequence Targeting Reagents
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      Fish
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      Antibodies
      Orthology
      No data available
      Engineered Foreign Genes
      Marker Marker Type Name
      EGFPEFGEGFP
      mCherryEFGmCherry
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      Mapping
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