Cel The life essential element iron is required as a cofactor in central nervous system metabolic processes, but unbound iron catalyzes the production of toxic reactive oxygen species. Neuronal iron accumulation is a common pathological feature in the cortex in Alzheimer’s disease (AD), the substantia nigra (SN) in Parkinson’s disease (PD), and the tauopathies. Since too much or too little iron can compromise cell viability, cellular iron homeostasis is tightly regulated. Ferroxidases, oxidize Fe2+ to Fe3+, and are essential for maintaining intracellular iron homeostasis. A deficiency in the surface presented ferroxidase leads to toxic iron accumulation and degeneration. Ferroxidase activities in the brain may fail with aging and a range of neurodegenerative disorders (ND), possibly contributing to disease pathogenesis.My group has discovered that the ferroxidase activity of β-amyloid precursor protein (APP) is essential for neuronal iron efflux and inhibited APP ferroxidase activity parallels iron accumulation in some ND. Disruption in the correct localization of a ferroxidase may be fundamental in the disease process. Of relevance, neuronal anterograde transport of APP requires tau and we have recently shown decreased tau expression impairs the presence of cell surface APP leading to inefficient efflux of iron and intensifying the risk of excitotoxicty within the region via intraneuronal iron accumulation.Primary aims will elucidate the role of APP trafficking and processing on iron efflux regulation within general neurobiology and investigate this mechanism in iron accumulating age- and pathologically- affected neurons already known to have problems with APP, tau and excitotoxicity.Some current therapeutic compounds for ND are proposed to work via restoring metal homeostasis. A final aim will determine if these compounds, as well as a number of novel derivatives, work through a pathway that restores APP to its correct function in neuronal iron efflux. Dziedzina nauki natural sciencesbiological sciencesneurobiologymedical and health sciencesbasic medicineneurologydementiaalzheimernatural sciencesbiological sciencesbiochemistrybiomoleculesproteinsmedical and health sciencesbasic medicineneurologyparkinsonmedical and health sciencesbasic medicinephysiologyhomeostasis Program(-y) FP7-PEOPLE - Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013) Temat(-y) FP7-PEOPLE-2012-CIG - Marie-Curie Action: "Career Integration Grants" Zaproszenie do składania wniosków FP7-PEOPLE-2012-CIG Zobacz inne projekty w ramach tego zaproszenia System finansowania MC-CIG - Support for training and career development of researcher (CIG) Koordynator UNIVERSITY OF LEEDS Wkład UE € 100 000,00 Adres WOODHOUSE LANE LS2 9JT Leeds Zjednoczone Królestwo Zobacz na mapie Region Yorkshire and the Humber West Yorkshire Leeds Rodzaj działalności Higher or Secondary Education Establishments Kontakt administracyjny Benjamin Williams (Mr.) Linki Kontakt z organizacją Opens in new window Strona internetowa Opens in new window Koszt całkowity Brak danych
