Structural and molecular myelination deficits occur prior to neuronal loss in the YAC128 and BACHD models of Huntington disease

Hum Mol Genet. 2016 Jul 1;25(13):2621-2632. doi: 10.1093/hmg/ddw122. Epub 2016 Apr 28.

Abstract

White matter (WM) atrophy is a significant feature of Huntington disease (HD), although its aetiology and early pathological manifestations remain poorly defined. In this study, we aimed to characterize WM-related features in the transgenic YAC128 and BACHD models of HD. Using diffusion tensor magnetic resonance imaging (DT-MRI), we demonstrate that microstructural WM abnormalities occur from an early age in YAC128 mice. Similarly, electron microscopy analysis of myelinated fibres of the corpus callosum indicated that myelin sheaths are thinner in YAC128 mice as early as 1.5 months of age, well before any neuronal loss can be detected. Transcript levels of myelin-related genes in striatal and cortical tissues were significantly lower in YAC128 mice from 2 weeks of age, and these findings were replicated in differentiated primary oligodendrocytes from YAC128 mice, suggesting a possible mechanistic explanation for the observed structural deficits. Concordant with these observations, we demonstrate reduced expression of myelin-related genes at 3 months of age and WM microstructural abnormalities using DT-MRI at 12 months of age in the BACHD rats. These findings indicate that WM deficits in HD are an early phenotype associated with cell-intrinsic effects of mutant huntingtin on myelin-related transcripts in oligodendrocytes, and raise the possibility that WM abnormalities may be an early contributing factor to the pathogenesis of HD.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Atrophy / pathology
  • Brain / metabolism
  • Corpus Callosum / metabolism
  • Corpus Striatum / metabolism
  • Diffusion Tensor Imaging / methods
  • Disease Models, Animal
  • Gene Expression
  • Humans
  • Huntington Disease / etiology
  • Huntington Disease / genetics*
  • Mice
  • Mice, Transgenic
  • Myelin Sheath / genetics
  • Myelin Sheath / metabolism
  • Myelin Sheath / physiology*
  • Neostriatum / metabolism
  • Nerve Tissue Proteins / genetics
  • Neurons / metabolism
  • Oligodendroglia / metabolism
  • Rats
  • White Matter / physiopathology*

Substances

  • Nerve Tissue Proteins