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Trophic Factor-Induced Activity ‘Signature’ Regulates the Functional Expression of Postsynaptic Excitatory Acetylcholine Receptors Required for Synaptogenesis
Highly coordinated and coincidental patterns of activity-dependent mechanisms (“fire together wire together”) are thought to serve as inductive signals during synaptogenesis, enabling neuronal pairing between specific sub-sets of excitatory partners. However, neither the nature of activity triggers,...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4381329/ https://www.ncbi.nlm.nih.gov/pubmed/25827640 http://dx.doi.org/10.1038/srep09523 |
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author | Luk, Collin C. Lee, Arthur J. Wijdenes, Pierre Zaidi, Wali Leung, Andrew Wong, Noelle Y. Andrews, Joseph Syed, Naweed I. |
author_facet | Luk, Collin C. Lee, Arthur J. Wijdenes, Pierre Zaidi, Wali Leung, Andrew Wong, Noelle Y. Andrews, Joseph Syed, Naweed I. |
author_sort | Luk, Collin C. |
collection | PubMed |
description | Highly coordinated and coincidental patterns of activity-dependent mechanisms (“fire together wire together”) are thought to serve as inductive signals during synaptogenesis, enabling neuronal pairing between specific sub-sets of excitatory partners. However, neither the nature of activity triggers, nor the “activity signature” of long-term neuronal firing in developing/regenerating neurons have yet been fully defined. Using a highly tractable model system comprising of identified cholinergic neurons from Lymnaea, we have discovered that intrinsic trophic factors present in the Lymnaea brain-conditioned medium (CM) act as a natural trigger for activity patterns in post- but not the presynaptic neuron. Using microelectrode array recordings, we demonstrate that trophic factors trigger stereotypical activity patterns that include changes in frequency, activity and variance. These parameters were reliable indicators of whether a neuron expressed functional excitatory or inhibitory nAChRs and synapse formation. Surprisingly, we found that the post- but not the presynaptic cell exhibits these changes in activity patterns, and that the functional expression of excitatory nAChRs required neuronal somata, de novo protein synthesis and voltage gated calcium channels. In summary, our data provides novel insights into trophic factor mediated actions on neuronal activity and its specific regulation of nAChR expression. |
format | Online Article Text |
id | pubmed-4381329 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-43813292015-04-07 Trophic Factor-Induced Activity ‘Signature’ Regulates the Functional Expression of Postsynaptic Excitatory Acetylcholine Receptors Required for Synaptogenesis Luk, Collin C. Lee, Arthur J. Wijdenes, Pierre Zaidi, Wali Leung, Andrew Wong, Noelle Y. Andrews, Joseph Syed, Naweed I. Sci Rep Article Highly coordinated and coincidental patterns of activity-dependent mechanisms (“fire together wire together”) are thought to serve as inductive signals during synaptogenesis, enabling neuronal pairing between specific sub-sets of excitatory partners. However, neither the nature of activity triggers, nor the “activity signature” of long-term neuronal firing in developing/regenerating neurons have yet been fully defined. Using a highly tractable model system comprising of identified cholinergic neurons from Lymnaea, we have discovered that intrinsic trophic factors present in the Lymnaea brain-conditioned medium (CM) act as a natural trigger for activity patterns in post- but not the presynaptic neuron. Using microelectrode array recordings, we demonstrate that trophic factors trigger stereotypical activity patterns that include changes in frequency, activity and variance. These parameters were reliable indicators of whether a neuron expressed functional excitatory or inhibitory nAChRs and synapse formation. Surprisingly, we found that the post- but not the presynaptic cell exhibits these changes in activity patterns, and that the functional expression of excitatory nAChRs required neuronal somata, de novo protein synthesis and voltage gated calcium channels. In summary, our data provides novel insights into trophic factor mediated actions on neuronal activity and its specific regulation of nAChR expression. Nature Publishing Group 2015-04-01 /pmc/articles/PMC4381329/ /pubmed/25827640 http://dx.doi.org/10.1038/srep09523 Text en Copyright © 2015, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Luk, Collin C. Lee, Arthur J. Wijdenes, Pierre Zaidi, Wali Leung, Andrew Wong, Noelle Y. Andrews, Joseph Syed, Naweed I. Trophic Factor-Induced Activity ‘Signature’ Regulates the Functional Expression of Postsynaptic Excitatory Acetylcholine Receptors Required for Synaptogenesis |
title | Trophic Factor-Induced Activity ‘Signature’ Regulates the Functional Expression of Postsynaptic Excitatory Acetylcholine Receptors Required for Synaptogenesis |
title_full | Trophic Factor-Induced Activity ‘Signature’ Regulates the Functional Expression of Postsynaptic Excitatory Acetylcholine Receptors Required for Synaptogenesis |
title_fullStr | Trophic Factor-Induced Activity ‘Signature’ Regulates the Functional Expression of Postsynaptic Excitatory Acetylcholine Receptors Required for Synaptogenesis |
title_full_unstemmed | Trophic Factor-Induced Activity ‘Signature’ Regulates the Functional Expression of Postsynaptic Excitatory Acetylcholine Receptors Required for Synaptogenesis |
title_short | Trophic Factor-Induced Activity ‘Signature’ Regulates the Functional Expression of Postsynaptic Excitatory Acetylcholine Receptors Required for Synaptogenesis |
title_sort | trophic factor-induced activity ‘signature’ regulates the functional expression of postsynaptic excitatory acetylcholine receptors required for synaptogenesis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4381329/ https://www.ncbi.nlm.nih.gov/pubmed/25827640 http://dx.doi.org/10.1038/srep09523 |
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