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Clusterin regulates β-amyloid toxicity via Dickkopf-1-driven induction of the wnt-PCP-JNK pathway

Authors :
Chantelle Fernandes
John Stephenson
Karelle Leroy
Alessia Usardi
Anbarasu Lourdusamy
Richard Williamson
Patrick M. Nolan
Elena M. Ribe
Wendy Noble
Angela Hodges
Christopher A. Reynolds
Richard Wroe
Chantal Bazenet
Claudie Hooper
Mirsada Causevic
Stuart Kellie
Alvina W.M. To
J-P. Brion
Raya Al-Shawi
Simon Lovestone
Katie Lunnon
Gerome Breen
Richard Dobson
Martha Robinson
J. Paul Simons
Simon J. Furney
Richard Killick
Kuang Lin
Bilal Malik
Source :
Molecular psychiatry, 19 (1, Molecular Psychiatry, Killick, R, Ribe, E M, Al-Shawi, R, Malik, B, Hooper, C, Fernandes, C, Dobson, R, Nolan, P M, Lourdusamy, A, Furney, S, Lin, K, Breen, G, Wroe, R, To, A W M, Leroy, K, Causevic, M, Usardi, A, Robinson, M, Noble, W, Williamson, R, Lunnon, K, Kellie, S, Reynolds, C H, Bazenet, C, Hodges, A, Brion, J-P, Stephenson, J, Paul Simons, J & Lovestone, S 2014, ' Clusterin regulates β-amyloid toxicity via Dickkopf-1-driven induction of the wnt-PCP-JNK pathway ', Molecular Psychiatry, vol. 19, no. 1, pp. 88-98 . https://doi.org/10.1038/mp.2012.163
Publication Year :
2012

Abstract

Although the mechanism of Aβ action in the pathogenesis of Alzheimer's disease (AD) has remained elusive, it is known to increase the expression of the antagonist of canonical wnt signalling, Dickkopf-1 (Dkk1), whereas the silencing of Dkk1 blocks Aβ neurotoxicity. We asked if clusterin, known to be regulated by wnt, is part of an Aβ/Dkk1 neurotoxic pathway. Knockdown of clusterin in primary neurons reduced Aβ toxicity and DKK1 upregulation and, conversely, Aβ increased intracellular clusterin and decreased clusterin protein secretion, resulting in the p53-dependent induction of DKK1. To further elucidate how the clusterin-dependent induction of Dkk1 by Aβ mediates neurotoxicity, we measured the effects of Aβ and Dkk1 protein on whole-genome expression in primary neurons, finding a common pathway suggestive of activation of wnt-planar cell polarity (PCP)-c-Jun N-terminal kinase (JNK) signalling leading to the induction of genes including EGR1 (early growth response-1), NAB2 (Ngfi-A-binding protein-2) and KLF10 (Krüppel-like factor-10) that, when individually silenced, protected against Aβ neurotoxicity and/or tau phosphorylation. Neuronal overexpression of Dkk1 in transgenic mice mimicked this Aβ-induced pathway and resulted in age-dependent increases in tau phosphorylation in hippocampus and cognitive impairment. Furthermore, we show that this Dkk1/wnt-PCP-JNK pathway is active in an Aβ-based mouse model of AD and in AD brain, but not in a tau-based mouse model or in frontotemporal dementia brain. Thus, we have identified a pathway whereby Aβ induces a clusterin/p53/Dkk1/wnt-PCP-JNK pathway, which drives the upregulation of several genes that mediate the development of AD-like neuropathologies, thereby providing new mechanistic insights into the action of Aβ in neurodegenerative diseases.Molecular Psychiatry advance online publication, 20 November 2012; doi:10.1038/mp.2012.163.<br />JOURNAL ARTICLE<br />SCOPUS: ar.j<br />info:eu-repo/semantics/published

Details

Database :
OpenAIRE
Journal :
Molecular psychiatry, 19 (1, Molecular Psychiatry, Killick, R, Ribe, E M, Al-Shawi, R, Malik, B, Hooper, C, Fernandes, C, Dobson, R, Nolan, P M, Lourdusamy, A, Furney, S, Lin, K, Breen, G, Wroe, R, To, A W M, Leroy, K, Causevic, M, Usardi, A, Robinson, M, Noble, W, Williamson, R, Lunnon, K, Kellie, S, Reynolds, C H, Bazenet, C, Hodges, A, Brion, J-P, Stephenson, J, Paul Simons, J & Lovestone, S 2014, ' Clusterin regulates β-amyloid toxicity via Dickkopf-1-driven induction of the wnt-PCP-JNK pathway ', Molecular Psychiatry, vol. 19, no. 1, pp. 88-98 . https://doi.org/10.1038/mp.2012.163
Accession number :
edsair.doi.dedup.....08d852d2e28fab1f69dcf47924b534aa
Full Text :
https://doi.org/10.1038/mp.2012.163