PUBLICATION

Modeling Environmentally-Induced Motor Neuron Degeneration in Zebrafish

Authors
Morrice, J.R., Gregory-Evans, C.Y., Shaw, C.A.
ID
ZDB-PUB-180322-5
Date
2018
Source
Scientific Reports   8: 4890 (Journal)
Registered Authors
Keywords
none
MeSH Terms
  • Amyotrophic Lateral Sclerosis/metabolism
  • Animals
  • Axons/metabolism
  • Disease Models, Animal
  • Hazardous Substances/adverse effects
  • Motor Neuron Disease/pathology*
  • Motor Neurons/metabolism
  • Nerve Degeneration/pathology*
  • Nervous System Malformations/metabolism
  • Neuromuscular Junction/metabolism
  • Superoxide Dismutase/metabolism
  • Zebrafish/metabolism
  • Zebrafish Proteins/metabolism
PubMed
29559645 Full text @ Sci. Rep.
CTD
29559645
Abstract
Zebrafish have been used to investigate motor neuron degeneration, including as a model system to examine the pathogenesis of amyotrophic lateral sclerosis (ALS). The use of zebrafish for this purpose has some advantages over other in vivo model systems. In the current paper, we show that bisphenol A (BPA) exposure in zebrafish embryos results in motor neuron degeneration with affected motor function, reduced motor axon length and branching, reduced neuromuscular junction integrity, motor neuron cell death and the presence of activated microglia. In zebrafish, motor axon length is the conventional method for estimating motor neuron degeneration, yet this measurement has not been confirmed as a valid surrogate marker. We also show that reduced motor axon length as measured from the sagittal plane is correlated with increased motor neuron cell death. Our preliminary timeline studies suggest that axonopathy precedes motor cell death. This outcome may have implications for early phase treatments of motor neuron degeneration.
Genes / Markers
Figures
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Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping