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Excitation Control: Balancing PSD-95 Function at the Synapse

Excitability of individual neurons dictates the overall excitation in specific brain circuits. This process is thought to be regulated by molecules that regulate synapse number, morphology and strength. Neuronal excitation is also influenced by the amounts of neurotransmitter receptors and signaling...

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Detalles Bibliográficos
Autores principales: Keith, Dove, El-Husseini, Alaa
Formato: Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2526002/
https://www.ncbi.nlm.nih.gov/pubmed/18946537
http://dx.doi.org/10.3389/neuro.02.004.2008
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author Keith, Dove
El-Husseini, Alaa
author_facet Keith, Dove
El-Husseini, Alaa
author_sort Keith, Dove
collection PubMed
description Excitability of individual neurons dictates the overall excitation in specific brain circuits. This process is thought to be regulated by molecules that regulate synapse number, morphology and strength. Neuronal excitation is also influenced by the amounts of neurotransmitter receptors and signaling molecules retained at particular synaptic sites. Recent studies revealed a key role for PSD-95, a scaffolding molecule enriched at glutamatergic synapses, in modulation of clustering of several neurotransmitter receptors, adhesion molecules, ion channels, cytoskeletal elements and signaling molecules at postsynaptic sites. In this review we will highlight mechanisms that control targeting of PSD-95 at the synapse, and discuss how this molecule influences the retention and clustering of diverse synaptic proteins to regulate synaptic structure and strength. We will also discuss how PSD-95 may maintain a balance between excitation and inhibition in the brain and how alterations in this balance may contribute to neuropsychiatric disorders.
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spelling pubmed-25260022008-10-22 Excitation Control: Balancing PSD-95 Function at the Synapse Keith, Dove El-Husseini, Alaa Front Mol Neurosci Neuroscience Excitability of individual neurons dictates the overall excitation in specific brain circuits. This process is thought to be regulated by molecules that regulate synapse number, morphology and strength. Neuronal excitation is also influenced by the amounts of neurotransmitter receptors and signaling molecules retained at particular synaptic sites. Recent studies revealed a key role for PSD-95, a scaffolding molecule enriched at glutamatergic synapses, in modulation of clustering of several neurotransmitter receptors, adhesion molecules, ion channels, cytoskeletal elements and signaling molecules at postsynaptic sites. In this review we will highlight mechanisms that control targeting of PSD-95 at the synapse, and discuss how this molecule influences the retention and clustering of diverse synaptic proteins to regulate synaptic structure and strength. We will also discuss how PSD-95 may maintain a balance between excitation and inhibition in the brain and how alterations in this balance may contribute to neuropsychiatric disorders. Frontiers Research Foundation 2008-03-28 /pmc/articles/PMC2526002/ /pubmed/18946537 http://dx.doi.org/10.3389/neuro.02.004.2008 Text en Copyright © 2008 Keith and El-Husseini. http://www.frontiersin.org/licenseagreement This is an open-access article subject to an exclusive license agreement between the authors and the Frontiers Research Foundation, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are credited.
spellingShingle Neuroscience
Keith, Dove
El-Husseini, Alaa
Excitation Control: Balancing PSD-95 Function at the Synapse
title Excitation Control: Balancing PSD-95 Function at the Synapse
title_full Excitation Control: Balancing PSD-95 Function at the Synapse
title_fullStr Excitation Control: Balancing PSD-95 Function at the Synapse
title_full_unstemmed Excitation Control: Balancing PSD-95 Function at the Synapse
title_short Excitation Control: Balancing PSD-95 Function at the Synapse
title_sort excitation control: balancing psd-95 function at the synapse
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2526002/
https://www.ncbi.nlm.nih.gov/pubmed/18946537
http://dx.doi.org/10.3389/neuro.02.004.2008
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