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B30 Investigating Hepatic Dysfunction In The Httq111/+ Mouse With A Perturbagen-based Primary Hepatocyte System
  1. R Weston1,
  2. J Rodier1,2,
  3. S Coffey1,
  4. A Glickenhaus1,
  5. LG Boros3,
  6. ME MacDonald4,
  7. JB Carroll1,4
  1. 1Western Washington University, 516 High St., Bellingham WA 98225, USA
  2. 2Université Claude Bernard Lyon 1, 43 Boulevard Du 11 Novembre 1918, 69100 Villeurbanne, France
  3. 3SiDMAP, 2990 S Sepulveda Blvd, Los Angeles, CA 90064, USA
  4. 4Massachusetts General Hospital, 55 Fruit St, Boston, MA 02114, USA


Background We are interested in mapping and understanding phenotypes that precede the development of overt signs of Huntington’s disease, in hopes of identifying pathways with the potential to be disease-modifying. Notably, the Huntington’s disease mutation is associated with early metabolic alterations of unknown aetiology in both humans and various model systems. Our own data suggest that widespread metabolic alterations occur very early in B6. HttQ111/Q7 mice, which precisely recapitulate the genetics of human HD patients.

Aims We aim to understand which tissues reveal the earliest transcriptional and metabolic changes in the B6. HttQ111/Q7 mice.

Methods We are applying stable isotope-based dynamic metabolic profiling (SiDMAP) to cells and tissues to quantify metabolic flux, and RNA sequencing (RNASeq) to quantify transcript abundance.

Results/outcome In a cross-tissue metabolic flux study of 90-day-old mice using U13C-glucose as a stable tracer, we observe that the most robust metabolic changes are observed in the liver. Transcriptomic analysis of matched samples with RNASeq reveals that the liver has more genotype-sensitive transcripts at this stage than does the striatum, the most vulnerable tissue in HD. Based on these in vivoresults, we hypothesise that very early changes in fatty acid synthesis, mobilisation and/or catabolism are occuring in the liver of HttQ111/+ mice. To study this hypothesis in more mechanistic detail, we have established a system of primary hepatocytes isolated from 90 day old mice fed one of 3 diets from weaning as a lipid-relevant perturbagen: high fat (65% kcal/fat), medium fat (45% kcal/fat) and normal chow (10% kcal/fat). We reason that examining phenotypes in HttQ111/Q7 cells at steady states may not be as informative as investigating their dynamic responses to chemically defined perturbations. Our phenotypic analysis in vitroincludes quantifying metabolic flux using multiple flux tracers (1,2–13C2-glucose and U13C-palmitate). We are also collecting transcriptomic data from matched samples using RNASeq, in hopes of identifying genotype-sensitive flux changes that are associated with coherent transcriptional alterations.

Conclusions We conclude that early transcriptional and metabolic flux changes occur in the livers of B6. HttQ111/Q7 mice.

  • Mouse models
  • metabolism
  • liver

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