Regional and progressive changes in brain expression of complexin II in a mouse transgenic for the Huntington's disease mutation

Brain Res Bull. 2004 Mar 1;63(1):45-55. doi: 10.1016/j.brainresbull.2003.12.004.

Abstract

Changes in mRNA expression of soluble NSF-attachment protein receptors (SNAREs) and SNARE-associated proteins have been shown to occur in a number of disorders such as schizophrenia, Alzheimer's disease and Parkinson's disease. We have shown previously that there is a decrease in protein levels of the SNARE-associated protein, complexin II (CPLXII) in Huntington's disease brain and in the R6/2 mouse model of Huntington's disease. In the current study, we used quantitative in situ hybridisation to examine mRNA expression of SNAREs (25 kDa synaptosome-associated protein (SNAP-25), syntaxin-1A and synaptobrevin-2) and SNARE-associated proteins (alpha-SNAP, CPLXI and CPLXII) in brain of R6/2 mice and their wild type littermates between 3 and 15 weeks of age. We found an early and progressive decrease of CPLXII expression in R6/2 mice brains. In contrast, no changes in SNARE expression were seen in R6/2 brains compared with wild type brain. Further, while decreased expression of alpha-SNAP and CPLXI was seen, this was not until 15 weeks of age and even then the changes were small. We suggest that downregulation of expression of mRNA encoding SNARE-associated proteins, first CPLXII and later CPLXI and alpha-SNAP, contributes to the progressive neuropathology of the R6/2 mouse model of Huntington's disease.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Vesicular Transport
  • Animals
  • Antigens, Surface / genetics
  • Brain / metabolism*
  • Brain / physiopathology
  • Brain Chemistry / genetics*
  • Carrier Proteins / genetics
  • Disease Models, Animal
  • Disease Progression
  • Down-Regulation / genetics
  • Exocytosis / genetics
  • Female
  • Huntington Disease / genetics
  • Huntington Disease / metabolism*
  • Huntington Disease / physiopathology
  • Male
  • Membrane Proteins / genetics*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred CBA
  • Mice, Transgenic
  • Nerve Tissue Proteins / genetics*
  • Presynaptic Terminals / metabolism*
  • R-SNARE Proteins
  • RNA, Messenger / metabolism
  • SNARE Proteins
  • Soluble N-Ethylmaleimide-Sensitive Factor Attachment Proteins
  • Synaptosomal-Associated Protein 25
  • Syntaxin 1
  • Vesicular Transport Proteins*

Substances

  • Adaptor Proteins, Vesicular Transport
  • Antigens, Surface
  • Carrier Proteins
  • Membrane Proteins
  • Nerve Tissue Proteins
  • R-SNARE Proteins
  • RNA, Messenger
  • SNARE Proteins
  • Snap25 protein, mouse
  • Soluble N-Ethylmaleimide-Sensitive Factor Attachment Proteins
  • Stx1a protein, mouse
  • Synaptosomal-Associated Protein 25
  • Syntaxin 1
  • Vesicular Transport Proteins
  • complexin I
  • complexin II