| Literature DB >> 24938402 |
Lydie Boussicault1, Anne-Sophie Hérard1, Noel Calingasan2, Fanny Petit1, Carole Malgorn1, Nicolas Merienne1, Caroline Jan1, Marie-Claude Gaillard1, Rodrigo Lerchundi3, Luis F Barros3, Carole Escartin1, Thierry Delzescaux1, Jean Mariani4, Philippe Hantraye1, M Flint Beal2, Emmanuel Brouillet1, Céline Véga4, Gilles Bonvento1.
Abstract
Huntington's disease (HD) is caused by cytosine-adenine-guanine (CAG) repeat expansions in the huntingtin (Htt) gene. Although early energy metabolic alterations in HD are likely to contribute to later neurodegenerative processes, the cellular and molecular mechanisms responsible for these metabolic alterations are not well characterized. Using the BACHD mice that express the full-length mutant huntingtin (mHtt) protein with 97 glutamine repeats, we first demonstrated localized in vivo changes in brain glucose use reminiscent of what is observed in premanifest HD carriers. Using biochemical, molecular, and functional analyses on different primary cell culture models from BACHD mice, we observed that mHtt does not directly affect metabolic activity in a cell autonomous manner. However, coculture of neurons with astrocytes from wild-type or BACHD mice identified mutant astrocytes as a source of adverse non-cell autonomous effects on neuron energy metabolism possibly by increasing oxidative stress. These results suggest that astrocyte-to-neuron signaling is involved in early energy metabolic alterations in HD.Entities:
Mesh:
Year: 2014 PMID: 24938402 PMCID: PMC4158666 DOI: 10.1038/jcbfm.2014.110
Source DB: PubMed Journal: J Cereb Blood Flow Metab ISSN: 0271-678X Impact factor: 6.200