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AIDA-1 Moves out of the Postsynaptic Density Core under Excitatory Conditions
AIDA-1 is highly enriched in postsynaptic density (PSD) fractions and is considered a major component of the PSD complex. In the present study, immunogold electron microscopy was applied to determine localization as well as the activity-induced redistribution of AIDA-1 at the PSD using two antibodie...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4565644/ https://www.ncbi.nlm.nih.gov/pubmed/26356309 http://dx.doi.org/10.1371/journal.pone.0137216 |
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author | Dosemeci, Ayse Toy, Dana Reese, Thomas S. Tao-Cheng, Jung-Hwa |
author_facet | Dosemeci, Ayse Toy, Dana Reese, Thomas S. Tao-Cheng, Jung-Hwa |
author_sort | Dosemeci, Ayse |
collection | PubMed |
description | AIDA-1 is highly enriched in postsynaptic density (PSD) fractions and is considered a major component of the PSD complex. In the present study, immunogold electron microscopy was applied to determine localization as well as the activity-induced redistribution of AIDA-1 at the PSD using two antibodies that recognize two different epitopes. In cultured rat hippocampal neurons under basal conditions, immunogold label for AIDA-1 is mostly located within the dense core of the PSD, with a median distance of ~30 nm from the postsynaptic membrane. Under excitatory conditions, such as depolarization with high K(+) (90 mM, 2 min) or application of NMDA (50 μM, 2 min), AIDA-1 label density at the PSD core is reduced to 40% of controls and the median distance of label from the postsynaptic membrane increases to ~55 nm. The effect of excitatory conditions on the postsynaptic distribution of AIDA-1 is reversed within 30 minutes after returning to control conditions. The reversible removal of AIDA-1 from the PSD core under excitatory conditions is similar to the redistribution of another abundant PSD protein, SynGAP. Both SynGAP-alpha1 and AIDA-1 are known to bind PSD-95. Activity-induced transient translocation of these abundant proteins from the PSD core could promote structural flexibility, vacate sites on PSD-95 for the insertion of other components and thus may create a window for synaptic modification. |
format | Online Article Text |
id | pubmed-4565644 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-45656442015-09-18 AIDA-1 Moves out of the Postsynaptic Density Core under Excitatory Conditions Dosemeci, Ayse Toy, Dana Reese, Thomas S. Tao-Cheng, Jung-Hwa PLoS One Research Article AIDA-1 is highly enriched in postsynaptic density (PSD) fractions and is considered a major component of the PSD complex. In the present study, immunogold electron microscopy was applied to determine localization as well as the activity-induced redistribution of AIDA-1 at the PSD using two antibodies that recognize two different epitopes. In cultured rat hippocampal neurons under basal conditions, immunogold label for AIDA-1 is mostly located within the dense core of the PSD, with a median distance of ~30 nm from the postsynaptic membrane. Under excitatory conditions, such as depolarization with high K(+) (90 mM, 2 min) or application of NMDA (50 μM, 2 min), AIDA-1 label density at the PSD core is reduced to 40% of controls and the median distance of label from the postsynaptic membrane increases to ~55 nm. The effect of excitatory conditions on the postsynaptic distribution of AIDA-1 is reversed within 30 minutes after returning to control conditions. The reversible removal of AIDA-1 from the PSD core under excitatory conditions is similar to the redistribution of another abundant PSD protein, SynGAP. Both SynGAP-alpha1 and AIDA-1 are known to bind PSD-95. Activity-induced transient translocation of these abundant proteins from the PSD core could promote structural flexibility, vacate sites on PSD-95 for the insertion of other components and thus may create a window for synaptic modification. Public Library of Science 2015-09-10 /pmc/articles/PMC4565644/ /pubmed/26356309 http://dx.doi.org/10.1371/journal.pone.0137216 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. |
spellingShingle | Research Article Dosemeci, Ayse Toy, Dana Reese, Thomas S. Tao-Cheng, Jung-Hwa AIDA-1 Moves out of the Postsynaptic Density Core under Excitatory Conditions |
title | AIDA-1 Moves out of the Postsynaptic Density Core under Excitatory Conditions |
title_full | AIDA-1 Moves out of the Postsynaptic Density Core under Excitatory Conditions |
title_fullStr | AIDA-1 Moves out of the Postsynaptic Density Core under Excitatory Conditions |
title_full_unstemmed | AIDA-1 Moves out of the Postsynaptic Density Core under Excitatory Conditions |
title_short | AIDA-1 Moves out of the Postsynaptic Density Core under Excitatory Conditions |
title_sort | aida-1 moves out of the postsynaptic density core under excitatory conditions |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4565644/ https://www.ncbi.nlm.nih.gov/pubmed/26356309 http://dx.doi.org/10.1371/journal.pone.0137216 |
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