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Astrocytes’ Contribution to Adult Neurogenesis in Physiology and Alzheimer’s Disease

Adult neurogenesis is one of the most drastic forms of brain plasticity in adulthood and there is a growing body of evidence showing that, in the hippocampus, this process contributes to mechanisms of memory as well as depression. Interestingly, adult neurogenesis is tightly regulated by the neuroge...

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Detalles Bibliográficos
Autores principales: Cassé, Frédéric, Richetin, Kevin, Toni, Nicolas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6277517/
https://www.ncbi.nlm.nih.gov/pubmed/30538622
http://dx.doi.org/10.3389/fncel.2018.00432
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author Cassé, Frédéric
Richetin, Kevin
Toni, Nicolas
author_facet Cassé, Frédéric
Richetin, Kevin
Toni, Nicolas
author_sort Cassé, Frédéric
collection PubMed
description Adult neurogenesis is one of the most drastic forms of brain plasticity in adulthood and there is a growing body of evidence showing that, in the hippocampus, this process contributes to mechanisms of memory as well as depression. Interestingly, adult neurogenesis is tightly regulated by the neurogenic niche, which provides a structural and molecular scaffold for stem cell proliferation and the differentiation and functional integration of new neurons. In this review, we highlight the role of astrocytes in the regulation of adult neurogenesis in the context of cognitive function. We also discuss how the changes in astrocytes function may dysregulate adult neurogenesis and contribute to cognitive impairment in the context of Alzheimer’s disease.
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spelling pubmed-62775172018-12-11 Astrocytes’ Contribution to Adult Neurogenesis in Physiology and Alzheimer’s Disease Cassé, Frédéric Richetin, Kevin Toni, Nicolas Front Cell Neurosci Neuroscience Adult neurogenesis is one of the most drastic forms of brain plasticity in adulthood and there is a growing body of evidence showing that, in the hippocampus, this process contributes to mechanisms of memory as well as depression. Interestingly, adult neurogenesis is tightly regulated by the neurogenic niche, which provides a structural and molecular scaffold for stem cell proliferation and the differentiation and functional integration of new neurons. In this review, we highlight the role of astrocytes in the regulation of adult neurogenesis in the context of cognitive function. We also discuss how the changes in astrocytes function may dysregulate adult neurogenesis and contribute to cognitive impairment in the context of Alzheimer’s disease. Frontiers Media S.A. 2018-11-27 /pmc/articles/PMC6277517/ /pubmed/30538622 http://dx.doi.org/10.3389/fncel.2018.00432 Text en Copyright © 2018 Cassé, Richetin and Toni. 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
Cassé, Frédéric
Richetin, Kevin
Toni, Nicolas
Astrocytes’ Contribution to Adult Neurogenesis in Physiology and Alzheimer’s Disease
title Astrocytes’ Contribution to Adult Neurogenesis in Physiology and Alzheimer’s Disease
title_full Astrocytes’ Contribution to Adult Neurogenesis in Physiology and Alzheimer’s Disease
title_fullStr Astrocytes’ Contribution to Adult Neurogenesis in Physiology and Alzheimer’s Disease
title_full_unstemmed Astrocytes’ Contribution to Adult Neurogenesis in Physiology and Alzheimer’s Disease
title_short Astrocytes’ Contribution to Adult Neurogenesis in Physiology and Alzheimer’s Disease
title_sort astrocytes’ contribution to adult neurogenesis in physiology and alzheimer’s disease
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6277517/
https://www.ncbi.nlm.nih.gov/pubmed/30538622
http://dx.doi.org/10.3389/fncel.2018.00432
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