The Wnt Receptor Ryk Reduces Neuronal and Cell Survival Capacity by Repressing FOXO Activity During the Early Phases of Mutant Huntingtin Pathogenicity
Web of Science
AuthorTourette, C; Farina, F; Vazquez-Manrique, RP; Orfila, A-M; Voisin, J; Hernandez, S; Offner, N; Parker, JA; Menet, S; Kim, J; ...
Source TitlePLoS Biology
PublisherPUBLIC LIBRARY SCIENCE
University of Melbourne Author/sStacker, Steven
AffiliationSir Peter MacCallum Department of Oncology
Document TypeJournal Article
CitationsTourette, C., Farina, F., Vazquez-Manrique, R. P., Orfila, A. -M., Voisin, J., Hernandez, S., Offner, N., Parker, J. A., Menet, S., Kim, J., Lyu, J., Choi, S. H., Cormier, K., Edgerly, C. K., Bordiuk, O. L., Smith, K., Louise, A., Halford, M., Stacker, S. ,... Neri, C. (2014). The Wnt Receptor Ryk Reduces Neuronal and Cell Survival Capacity by Repressing FOXO Activity During the Early Phases of Mutant Huntingtin Pathogenicity. PLOS BIOLOGY, 12 (6), https://doi.org/10.1371/journal.pbio.1001895.
Access StatusOpen Access
The Wnt receptor Ryk is an evolutionary-conserved protein important during neuronal differentiation through several mechanisms, including γ-secretase cleavage and nuclear translocation of its intracellular domain (Ryk-ICD). Although the Wnt pathway may be neuroprotective, the role of Ryk in neurodegenerative disease remains unknown. We found that Ryk is up-regulated in neurons expressing mutant huntingtin (HTT) in several models of Huntington's disease (HD). Further investigation in Caenorhabditis elegans and mouse striatal cell models of HD provided a model in which the early-stage increase of Ryk promotes neuronal dysfunction by repressing the neuroprotective activity of the longevity-promoting factor FOXO through a noncanonical mechanism that implicates the Ryk-ICD fragment and its binding to the FOXO co-factor β-catenin. The Ryk-ICD fragment suppressed neuroprotection by lin-18/Ryk loss-of-function in expanded-polyQ nematodes, repressed FOXO transcriptional activity, and abolished β-catenin protection of mutant htt striatal cells against cell death vulnerability. Additionally, Ryk-ICD was increased in the nucleus of mutant htt cells, and reducing γ-secretase PS1 levels compensated for the cytotoxicity of full-length Ryk in these cells. These findings reveal that the Ryk-ICD pathway may impair FOXO protective activity in mutant polyglutamine neurons, suggesting that neurons are unable to efficiently maintain function and resist disease from the earliest phases of the pathogenic process in HD.
- Click on "Export Reference in RIS Format" and choose "open with... Endnote".
- Click on "Export Reference in RIS Format". Login to Refworks, go to References => Import References