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Wnt Signaling Deregulation in the Aging and Alzheimer’s Brain

Growing evidence suggests that synaptic signaling is compromised in the aging brain and in Alzheimer’s disease (AD), contributing to synaptic decline. Wnt signaling is a prominent pathway at the synapse and is required for synaptic plasticity and maintenance in the adult brain. In this review, we su...

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Autores principales: Palomer, Ernest, Buechler, Johanna, Salinas, Patricia C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6538920/
https://www.ncbi.nlm.nih.gov/pubmed/31191253
http://dx.doi.org/10.3389/fncel.2019.00227
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author Palomer, Ernest
Buechler, Johanna
Salinas, Patricia C.
author_facet Palomer, Ernest
Buechler, Johanna
Salinas, Patricia C.
author_sort Palomer, Ernest
collection PubMed
description Growing evidence suggests that synaptic signaling is compromised in the aging brain and in Alzheimer’s disease (AD), contributing to synaptic decline. Wnt signaling is a prominent pathway at the synapse and is required for synaptic plasticity and maintenance in the adult brain. In this review, we summarize the current knowledge on deregulation of Wnt signaling in the context of aging and AD. Emerging studies suggest that enhancing Wnt signaling could boost synaptic function during aging, and ameliorate synaptic pathology in AD. Although further research is needed to determine the precise contribution of deficient Wnt signaling to AD pathogenesis, targeting Wnt signaling components may provide novel therapeutic avenues for synapse protection or restoration in the brain.
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spelling pubmed-65389202019-06-12 Wnt Signaling Deregulation in the Aging and Alzheimer’s Brain Palomer, Ernest Buechler, Johanna Salinas, Patricia C. Front Cell Neurosci Neuroscience Growing evidence suggests that synaptic signaling is compromised in the aging brain and in Alzheimer’s disease (AD), contributing to synaptic decline. Wnt signaling is a prominent pathway at the synapse and is required for synaptic plasticity and maintenance in the adult brain. In this review, we summarize the current knowledge on deregulation of Wnt signaling in the context of aging and AD. Emerging studies suggest that enhancing Wnt signaling could boost synaptic function during aging, and ameliorate synaptic pathology in AD. Although further research is needed to determine the precise contribution of deficient Wnt signaling to AD pathogenesis, targeting Wnt signaling components may provide novel therapeutic avenues for synapse protection or restoration in the brain. Frontiers Media S.A. 2019-05-22 /pmc/articles/PMC6538920/ /pubmed/31191253 http://dx.doi.org/10.3389/fncel.2019.00227 Text en Copyright © 2019 Palomer, Buechler and Salinas. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Palomer, Ernest
Buechler, Johanna
Salinas, Patricia C.
Wnt Signaling Deregulation in the Aging and Alzheimer’s Brain
title Wnt Signaling Deregulation in the Aging and Alzheimer’s Brain
title_full Wnt Signaling Deregulation in the Aging and Alzheimer’s Brain
title_fullStr Wnt Signaling Deregulation in the Aging and Alzheimer’s Brain
title_full_unstemmed Wnt Signaling Deregulation in the Aging and Alzheimer’s Brain
title_short Wnt Signaling Deregulation in the Aging and Alzheimer’s Brain
title_sort wnt signaling deregulation in the aging and alzheimer’s brain
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6538920/
https://www.ncbi.nlm.nih.gov/pubmed/31191253
http://dx.doi.org/10.3389/fncel.2019.00227
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