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Neuronal epigenetics and the aging synapse
Two of the most salient phenotypes of aging are cognitive decline and loss of motor function, both of which are controlled by the nervous system. Cognition and muscle contraction require that neuronal synapses develop and maintain proper structure and function. We review the literature on how normal...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4444820/ https://www.ncbi.nlm.nih.gov/pubmed/26074775 http://dx.doi.org/10.3389/fncel.2015.00208 |
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author | Azpurua, Jorge Eaton, Benjamin A. |
author_facet | Azpurua, Jorge Eaton, Benjamin A. |
author_sort | Azpurua, Jorge |
collection | PubMed |
description | Two of the most salient phenotypes of aging are cognitive decline and loss of motor function, both of which are controlled by the nervous system. Cognition and muscle contraction require that neuronal synapses develop and maintain proper structure and function. We review the literature on how normal physiological aging disrupts central and peripheral synapse function including the degradation of structure and/or control of neurotransmission. Here we also attempt to connect the work done on the epigenetics of aging to the growing literature of how epigenetic mechanisms control synapse structure and function. Lastly, we address possible roles of epigenetic mechanisms to explain why the basal rates of age-related dysfunction vary so widely across individuals. |
format | Online Article Text |
id | pubmed-4444820 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-44448202015-06-12 Neuronal epigenetics and the aging synapse Azpurua, Jorge Eaton, Benjamin A. Front Cell Neurosci Neuroscience Two of the most salient phenotypes of aging are cognitive decline and loss of motor function, both of which are controlled by the nervous system. Cognition and muscle contraction require that neuronal synapses develop and maintain proper structure and function. We review the literature on how normal physiological aging disrupts central and peripheral synapse function including the degradation of structure and/or control of neurotransmission. Here we also attempt to connect the work done on the epigenetics of aging to the growing literature of how epigenetic mechanisms control synapse structure and function. Lastly, we address possible roles of epigenetic mechanisms to explain why the basal rates of age-related dysfunction vary so widely across individuals. Frontiers Media S.A. 2015-05-27 /pmc/articles/PMC4444820/ /pubmed/26074775 http://dx.doi.org/10.3389/fncel.2015.00208 Text en Copyright © 2015 Azpurua and Eaton. 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 and reproduction in other forums is permitted, provided the original author(s) or licensor 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 Azpurua, Jorge Eaton, Benjamin A. Neuronal epigenetics and the aging synapse |
title | Neuronal epigenetics and the aging synapse |
title_full | Neuronal epigenetics and the aging synapse |
title_fullStr | Neuronal epigenetics and the aging synapse |
title_full_unstemmed | Neuronal epigenetics and the aging synapse |
title_short | Neuronal epigenetics and the aging synapse |
title_sort | neuronal epigenetics and the aging synapse |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4444820/ https://www.ncbi.nlm.nih.gov/pubmed/26074775 http://dx.doi.org/10.3389/fncel.2015.00208 |
work_keys_str_mv | AT azpuruajorge neuronalepigeneticsandtheagingsynapse AT eatonbenjamina neuronalepigeneticsandtheagingsynapse |