Selective enrichment of DJ-1 protein in primate striatal neuronal processes: implications for Parkinson's disease

J Comp Neurol. 2007 Jan 20;500(3):585-99. doi: 10.1002/cne.21191.

Abstract

Mutations in DJ-1 cause autosomal recessive, early-onset Parkinson's disease (PD). The precise function and distribution of DJ-1 in the central nervous system remain unclear. In this study, we performed a comprehensive analysis of DJ-1 expression in human, monkey, and rat brains with antibodies that recognize distinct, evolutionarily conserved epitopes of DJ-1. We found that DJ-1 displays region-specific neuronal and glial labeling in human and nonhuman primate brain, sharply contrasting with the primarily neuronal expression pattern observed throughout rat brain. Further immunohistochemical analysis of DJ-1 expression in human and nonhuman primate brains showed that DJ-1 protein is expressed in neurons within the substantia nigra pars compacta and striatum, two regions critically involved in PD pathogenesis. Moreover, immunoelectron microscopic analysis revealed a selective enrichment of DJ-1 within primate striatal axons, presynaptic terminals, and dendritic spines with respect to the DJ-1 expression in prefrontal cortex. Together, these findings indicate neuronal and synaptic expression of DJ-1 in primate subcortical brain regions and suggest a physiological role for DJ-1 in the survival and/or function of nigral-striatal neurons.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural

MeSH terms

  • Aged
  • Aged, 80 and over
  • Animals
  • Antibody Specificity
  • Conserved Sequence
  • Corpus Striatum / metabolism*
  • Corpus Striatum / physiopathology
  • Corpus Striatum / ultrastructure
  • Dendritic Spines / metabolism
  • Dendritic Spines / ultrastructure
  • Epitopes / chemistry
  • Evolution, Molecular
  • Female
  • Humans
  • Immunohistochemistry
  • Intracellular Signaling Peptides and Proteins / metabolism*
  • Macaca mulatta
  • Male
  • Mice
  • Mice, Knockout
  • Microscopy, Immunoelectron
  • Neurons / metabolism*
  • Neurons / ultrastructure
  • Oncogene Proteins / metabolism*
  • Parkinson Disease / metabolism*
  • Parkinson Disease / physiopathology
  • Phylogeny
  • Presynaptic Terminals / metabolism
  • Presynaptic Terminals / ultrastructure
  • Protein Deglycase DJ-1
  • Rats
  • Substantia Nigra / metabolism
  • Substantia Nigra / physiopathology
  • Substantia Nigra / ultrastructure

Substances

  • Epitopes
  • Intracellular Signaling Peptides and Proteins
  • Oncogene Proteins
  • PARK7 protein, human
  • Protein Deglycase DJ-1