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GSK-3 and Wnt Signaling in Neurogenesis and Bipolar Disorder

The canonical Wnt signaling pathway is critical for development of the mammalian central nervous system and regulates diverse processes throughout adulthood, including adult neurogenesis. Glycogen synthase kinase-3 (GSK-3) antagonizes the canonical Wnt pathway and therefore also plays a central role...

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Detalles Bibliográficos
Autores principales: Valvezan, Alexander J., Klein, Peter S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3268224/
https://www.ncbi.nlm.nih.gov/pubmed/22319467
http://dx.doi.org/10.3389/fnmol.2012.00001
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author Valvezan, Alexander J.
Klein, Peter S.
author_facet Valvezan, Alexander J.
Klein, Peter S.
author_sort Valvezan, Alexander J.
collection PubMed
description The canonical Wnt signaling pathway is critical for development of the mammalian central nervous system and regulates diverse processes throughout adulthood, including adult neurogenesis. Glycogen synthase kinase-3 (GSK-3) antagonizes the canonical Wnt pathway and therefore also plays a central role in neural development and adult neurogenesis. Lithium, the first line of therapy for bipolar disorder, inhibits GSK-3, activates Wnt signaling and stimulates adult neurogenesis, which may be important for its therapeutic effects. GSK-3 also regulates other critical signaling pathways which may contribute to the therapeutic effects of lithium, including growth factor/neurotrophin signaling downstream of Akt. Here we will review the roles of GSK-3 in CNS development and adult neurogenesis, with a focus on the canonical Wnt pathway. We will also discuss the validation of GSK-3 as the relevant target of lithium and the mechanisms downstream of GSK-3 that influence mammalian behavior.
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spelling pubmed-32682242012-02-08 GSK-3 and Wnt Signaling in Neurogenesis and Bipolar Disorder Valvezan, Alexander J. Klein, Peter S. Front Mol Neurosci Neuroscience The canonical Wnt signaling pathway is critical for development of the mammalian central nervous system and regulates diverse processes throughout adulthood, including adult neurogenesis. Glycogen synthase kinase-3 (GSK-3) antagonizes the canonical Wnt pathway and therefore also plays a central role in neural development and adult neurogenesis. Lithium, the first line of therapy for bipolar disorder, inhibits GSK-3, activates Wnt signaling and stimulates adult neurogenesis, which may be important for its therapeutic effects. GSK-3 also regulates other critical signaling pathways which may contribute to the therapeutic effects of lithium, including growth factor/neurotrophin signaling downstream of Akt. Here we will review the roles of GSK-3 in CNS development and adult neurogenesis, with a focus on the canonical Wnt pathway. We will also discuss the validation of GSK-3 as the relevant target of lithium and the mechanisms downstream of GSK-3 that influence mammalian behavior. Frontiers Research Foundation 2012-01-30 /pmc/articles/PMC3268224/ /pubmed/22319467 http://dx.doi.org/10.3389/fnmol.2012.00001 Text en Copyright © 2012 Valvezan and Klein. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited.
spellingShingle Neuroscience
Valvezan, Alexander J.
Klein, Peter S.
GSK-3 and Wnt Signaling in Neurogenesis and Bipolar Disorder
title GSK-3 and Wnt Signaling in Neurogenesis and Bipolar Disorder
title_full GSK-3 and Wnt Signaling in Neurogenesis and Bipolar Disorder
title_fullStr GSK-3 and Wnt Signaling in Neurogenesis and Bipolar Disorder
title_full_unstemmed GSK-3 and Wnt Signaling in Neurogenesis and Bipolar Disorder
title_short GSK-3 and Wnt Signaling in Neurogenesis and Bipolar Disorder
title_sort gsk-3 and wnt signaling in neurogenesis and bipolar disorder
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3268224/
https://www.ncbi.nlm.nih.gov/pubmed/22319467
http://dx.doi.org/10.3389/fnmol.2012.00001
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