Journal article
Paradoxical condensation of copper with elevated β-amyloid in lipid rafts under cellular copper deficiency conditions. Implications for Alzheimer disease
YH Hung, EL Robb, I Voltakis, M Ho, G Evin, QX Li, JG Culvenor, CL Masters, RA Cherny, AI Bush
Journal of Biological Chemistry | AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC | Published : 2009
Abstract
Redox-active copper is implicated in the pathogenesis of Alzheimer disease (AD), β-amyloid peptide (Aβ) aggregation, and amyloid formation. Aβ·copper complexes have been identified in AD and catalytically oxidize cholesterol and lipid to generate H2O2 and lipid peroxides. The site and mechanism of this abnormality is not known. Growing evidence suggests that amyloidogenic processing of the β-amyloid precursor protein (APP) occurs in lipid rafts, membrane microdomains enriched in cholesterol. β- and γ-secretases, and Aβ have been identified in lipid rafts in cultured cells, human and rodent brains, but the role of copper in lipid raft amyloidogenic processing is presently unknown. In this stu..
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Funding Acknowledgements
This work was supported by an Alzheimer's Association Zenith Award (to A. I. B.) and grants (to A. I. B.) from the American Health Assistance Foundation, Australian Research Council, Bethlehem Griffiths Research Foundation, and National Health and Medical Research Council (Australia).