PUBLICATION

Overexpression of mutant superoxide dismutase 1 causes a motor axonopathy in the zebrafish

Authors
Lemmens, R., Van Hoecke, A., Hersmus, N., Geelen, V., D'Hollander, I., Thijs, V., Van Den Bosch, L., Carmeliet, P., and Robberecht, W.
ID
ZDB-PUB-070726-21
Date
2007
Source
Human molecular genetics   16(19): 2359-2365 (Journal)
Registered Authors
Keywords
none
MeSH Terms
  • Animals
  • Blotting, Western
  • Humans
  • Immunohistochemistry
  • Motor Neuron Disease/enzymology
  • Motor Neuron Disease/genetics*
  • Motor Neuron Disease/pathology
  • Mutation*
  • RNA, Messenger/genetics
  • RNA, Messenger/metabolism
  • Superoxide Dismutase/genetics*
  • Superoxide Dismutase/metabolism
  • Vascular Endothelial Growth Factor A/genetics
  • Vascular Endothelial Growth Factor A/metabolism
  • Zebrafish
PubMed
17636250 Full text @ Hum. Mol. Genet.
Abstract
The development of small animal models is of major interest to unravel the pathogenesis and treatment of neurodegenerative diseases, especially because of their potential in large-scale chemical and genetic screening. We have investigated the zebrafish as a model to study amyotrophic lateral sclerosis (ALS), a fatal neurodegenerative disorder characterized by the selective loss of motor neurons, caused by mutations in superoxide dismutase 1 (SOD1) in a subset of patients. Overexpression of mutant human SOD1 in zebrafish embryos induced a motor axonopathy that was specific, dose-dependent and found for all mutations studied. Moreover, using this newly established animal model for ALS we investigated the role of a known modifier in the disease: vascular endothelial growth factor (VEGF). Lowering VEGF induced a more severe phenotype while upregulating VEGF rescued the mutant SOD1 axonopathy. This novel zebrafish model underscores the potential of VEGF for the treatment of ALS and furthermore will permit large scale genetic and chemical screening to facilitate the identification of new therapeutic targets in motor neuron disease.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping