header logo image header logo text
Downloads Login
Research
General Information
ZIRC
ZFIN ID: ZDB-PUB-080826-16
Loss of PINK1 function affects development and results in neurodegeneration in zebrafish
Anichtchik, O., Diekmann, H., Fleming, A., Roach, A., Goldsmith, P., and Rubinsztein, D.C.
Date: 2008
Source: The Journal of neuroscience : the official journal of the Society for Neuroscience   28(33): 8199-8207 (Journal)
Registered Authors: Anichtchik, Oleg, Diekmann, Heike, Fleming, Angeleen
Keywords: Parkinson's disease, zebrafish, neurodegeneration, mitochondria, ROS, PINK1
MeSH Terms:
  • Animals
  • Axons/enzymology
  • Axons/pathology
  • Cell Death/genetics
  • Gene Expression Regulation, Developmental/genetics
  • Humans
  • Nerve Degeneration/embryology
  • Nerve Degeneration/enzymology*
  • Nerve Degeneration/genetics*
  • Nerve Degeneration/pathology
  • Neurons/enzymology
  • Neurons/pathology
  • Phenotype
  • Protein Kinases/deficiency*
  • Protein Kinases/genetics*
  • Protein Kinases/physiology
  • Zebrafish
  • Zebrafish Proteins/deficiency*
  • Zebrafish Proteins/genetics*
  • Zebrafish Proteins/physiology
PubMed: 18701682 Full text @ J. Neurosci.
FIGURES
ABSTRACT
Parkinson's disease (PD) is the second most prevalent neurodegenerative disorder in the Western world. PTEN (phosphatase/tensin homolog on chromosome 10)-induced putative kinase 1 (PINK1), a putative kinase that is mutated in autosomal recessive forms of PD, is also implicated in sporadic cases of the disease. Although the mutations appear to result in a loss of function, the roles of this protein and the pathways involved in PINK1 PD are poorly understood. Here, we generated a vertebrate model of PINK1 insufficiency using morpholino oligonucleotide knockdown in zebrafish (Danio rerio). PINK1 knockdown results in a severe developmental phenotype that is rescued by wild-type human PINK1 mRNA. Morphants display a moderate decrease in the numbers of central dopaminergic neurons and alterations of mitochondrial function, including increases in caspase-3 activity and reactive oxygen species (ROS) levels. When the morphants were exposed to several drugs with antioxidant properties, ROS levels were normalized and the associated phenotype improved. In addition, GSK3beta-related mechanisms can account for some of the effects of PINK1 knockdown, as morphant fish show elevated GSK3beta activity and their phenotype is partially abrogated by GSK3beta inhibitors, such as LiCl and SB216763 [3-(2,4-dichlorophenyl)-4-(1-methyl-1H-indol-3-yl)1H-pyrrole-2,5-dione]. This provides new insights into the biology of PINK1 and a possible therapeutic avenue for further investigation.
ADDITIONAL INFORMATION