| Literature DB >> 25419706 |
Monica K Wetzel-Smith1, Julie Hunkapiller2, Tushar R Bhangale3, Karpagam Srinivasan1, Janice A Maloney1, Jasvinder K Atwal1, Susan M Sa4, Murat B Yaylaoglu4, Oded Foreman4, Ward Ortmann2, Nisha Rathore2, David V Hansen1, Marc Tessier-Lavigne5, Richard Mayeux6, Margaret Pericak-Vance7, Jonathan Haines8, Lindsay A Farrer9, Gerard D Schellenberg10, Alison Goate11, Timothy W Behrens2, Carlos Cruchaga12, Ryan J Watts1, Robert R Graham2.
Abstract
We have identified a rare coding mutation, T835M (rs137875858), in the UNC5C netrin receptor gene that segregated with disease in an autosomal dominant pattern in two families enriched for late-onset Alzheimer's disease and that was associated with disease across four large case-control cohorts (odds ratio = 2.15, Pmeta = 0.0095). T835M alters a conserved residue in the hinge region of UNC5C, and in vitro studies demonstrate that this mutation leads to increased cell death in human HEK293T cells and in rodent neurons. Furthermore, neurons expressing T835M UNC5C are more susceptible to cell death from multiple neurotoxic stimuli, including β-amyloid (Aβ), glutamate and staurosporine. On the basis of these data and the enriched hippocampal expression of UNC5C in the adult nervous system, we propose that one possible mechanism in which T835M UNC5C contributes to the risk of Alzheimer's disease is by increasing susceptibility to neuronal cell death, particularly in vulnerable regions of the Alzheimer's disease brain.Entities:
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Year: 2014 PMID: 25419706 PMCID: PMC4301587 DOI: 10.1038/nm.3736
Source DB: PubMed Journal: Nat Med ISSN: 1078-8956 Impact factor: 53.440