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Membrane-targeted strategies for modulating APP and Aβ-mediated toxicity

Alzheimer's disease (AD) is a progressive neurodegenerative disease characterized by numerous pathological features including the accumulation of neurotoxic amyloid-β (Aβ) peptide. There is currently no effective therapy for AD, but the development of therapeutic strategies that target the cell...

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Detalles Bibliográficos
Autores principales: Price, Katherine A, Crouch, Peter J, Donnelly, Paul S, Masters, Colin L, White, Anthony R, Curtain, Cyril C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3823352/
https://www.ncbi.nlm.nih.gov/pubmed/19278455
http://dx.doi.org/10.1111/j.1582-4934.2008.00642.x
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author Price, Katherine A
Crouch, Peter J
Donnelly, Paul S
Masters, Colin L
White, Anthony R
Curtain, Cyril C
author_facet Price, Katherine A
Crouch, Peter J
Donnelly, Paul S
Masters, Colin L
White, Anthony R
Curtain, Cyril C
author_sort Price, Katherine A
collection PubMed
description Alzheimer's disease (AD) is a progressive neurodegenerative disease characterized by numerous pathological features including the accumulation of neurotoxic amyloid-β (Aβ) peptide. There is currently no effective therapy for AD, but the development of therapeutic strategies that target the cell membrane is gaining increased interest. The amyloid precursor protein (APP) from which Aβ is formed is a membrane-bound protein, and Aβ production and toxicity are both membrane mediated events. This review describes the critical role of cell membranes in AD with particular emphasis on how the composition and structure of the membrane and its specialized regions may influence toxic or benign Aβ/APP pathways in AD. The putative role of copper (Cu) in AD is also discussed, and we highlight how targeting the cell membrane with Cu complexes has therapeutic potential in AD.
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spelling pubmed-38233522015-04-27 Membrane-targeted strategies for modulating APP and Aβ-mediated toxicity Price, Katherine A Crouch, Peter J Donnelly, Paul S Masters, Colin L White, Anthony R Curtain, Cyril C J Cell Mol Med Reviews Alzheimer's disease (AD) is a progressive neurodegenerative disease characterized by numerous pathological features including the accumulation of neurotoxic amyloid-β (Aβ) peptide. There is currently no effective therapy for AD, but the development of therapeutic strategies that target the cell membrane is gaining increased interest. The amyloid precursor protein (APP) from which Aβ is formed is a membrane-bound protein, and Aβ production and toxicity are both membrane mediated events. This review describes the critical role of cell membranes in AD with particular emphasis on how the composition and structure of the membrane and its specialized regions may influence toxic or benign Aβ/APP pathways in AD. The putative role of copper (Cu) in AD is also discussed, and we highlight how targeting the cell membrane with Cu complexes has therapeutic potential in AD. Blackwell Publishing Ltd 2009-02 2008-12-29 /pmc/articles/PMC3823352/ /pubmed/19278455 http://dx.doi.org/10.1111/j.1582-4934.2008.00642.x Text en © 2009 The Authors Journal compilation © 2009 Foundation for Cellular and Molecular Medicine/Blackwell Publishing Ltd
spellingShingle Reviews
Price, Katherine A
Crouch, Peter J
Donnelly, Paul S
Masters, Colin L
White, Anthony R
Curtain, Cyril C
Membrane-targeted strategies for modulating APP and Aβ-mediated toxicity
title Membrane-targeted strategies for modulating APP and Aβ-mediated toxicity
title_full Membrane-targeted strategies for modulating APP and Aβ-mediated toxicity
title_fullStr Membrane-targeted strategies for modulating APP and Aβ-mediated toxicity
title_full_unstemmed Membrane-targeted strategies for modulating APP and Aβ-mediated toxicity
title_short Membrane-targeted strategies for modulating APP and Aβ-mediated toxicity
title_sort membrane-targeted strategies for modulating app and aβ-mediated toxicity
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3823352/
https://www.ncbi.nlm.nih.gov/pubmed/19278455
http://dx.doi.org/10.1111/j.1582-4934.2008.00642.x
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