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Ca(2+)-permeable AMPA receptors in homeostatic synaptic plasticity

Neurons possess diverse mechanisms of homeostatic adaptation to overall changes in neural and synaptic activity, which are critical for proper brain functions. Homeostatic regulation of excitatory synapses has been studied in the context of synaptic scaling, which allows neurons to adjust their exci...

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Autor principal: Lee, Hey-Kyoung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3278195/
https://www.ncbi.nlm.nih.gov/pubmed/22347846
http://dx.doi.org/10.3389/fnmol.2012.00017
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author Lee, Hey-Kyoung
author_facet Lee, Hey-Kyoung
author_sort Lee, Hey-Kyoung
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description Neurons possess diverse mechanisms of homeostatic adaptation to overall changes in neural and synaptic activity, which are critical for proper brain functions. Homeostatic regulation of excitatory synapses has been studied in the context of synaptic scaling, which allows neurons to adjust their excitatory synaptic gain to maintain their activity within a dynamic range. Recent evidence suggests that one of the main mechanisms underlying synaptic scaling is by altering the function of postsynaptic α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors (AMPARs), including synaptic expression of Ca(2+)-permeable (CP-) AMPARs. CP-AMPARs endow synapses with unique properties, which may benefit adaptation of neurons to periods of inactivity as would occur when a major input is lost. This review will summarize how synaptic expression of CP-AMPARs is regulated during homeostatic synaptic plasticity in the context of synaptic scaling, and will address the potential functional consequences of altering synaptic CP-AMPAR content.
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spelling pubmed-32781952012-02-17 Ca(2+)-permeable AMPA receptors in homeostatic synaptic plasticity Lee, Hey-Kyoung Front Mol Neurosci Neuroscience Neurons possess diverse mechanisms of homeostatic adaptation to overall changes in neural and synaptic activity, which are critical for proper brain functions. Homeostatic regulation of excitatory synapses has been studied in the context of synaptic scaling, which allows neurons to adjust their excitatory synaptic gain to maintain their activity within a dynamic range. Recent evidence suggests that one of the main mechanisms underlying synaptic scaling is by altering the function of postsynaptic α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors (AMPARs), including synaptic expression of Ca(2+)-permeable (CP-) AMPARs. CP-AMPARs endow synapses with unique properties, which may benefit adaptation of neurons to periods of inactivity as would occur when a major input is lost. This review will summarize how synaptic expression of CP-AMPARs is regulated during homeostatic synaptic plasticity in the context of synaptic scaling, and will address the potential functional consequences of altering synaptic CP-AMPAR content. Frontiers Media S.A. 2012-02-13 /pmc/articles/PMC3278195/ /pubmed/22347846 http://dx.doi.org/10.3389/fnmol.2012.00017 Text en Copyright © 2012 Lee. 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
Lee, Hey-Kyoung
Ca(2+)-permeable AMPA receptors in homeostatic synaptic plasticity
title Ca(2+)-permeable AMPA receptors in homeostatic synaptic plasticity
title_full Ca(2+)-permeable AMPA receptors in homeostatic synaptic plasticity
title_fullStr Ca(2+)-permeable AMPA receptors in homeostatic synaptic plasticity
title_full_unstemmed Ca(2+)-permeable AMPA receptors in homeostatic synaptic plasticity
title_short Ca(2+)-permeable AMPA receptors in homeostatic synaptic plasticity
title_sort ca(2+)-permeable ampa receptors in homeostatic synaptic plasticity
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3278195/
https://www.ncbi.nlm.nih.gov/pubmed/22347846
http://dx.doi.org/10.3389/fnmol.2012.00017
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