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Network oscillation rules imposed by species-specific electrical coupling
Electrical junctions are widespread within the mammalian CNS. Yet, their role in organizing neuronal ensemble activity remains incompletely understood. Here, in a functionally well-characterized system – neuroendocrine tuberoinfundibular dopamine (TIDA) neurons - we demonstrate a striking species di...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5933921/ https://www.ncbi.nlm.nih.gov/pubmed/29722649 http://dx.doi.org/10.7554/eLife.33144 |
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author | Stagkourakis, Stefanos Pérez, Carolina Thörn Hellysaz, Arash Ammari, Rachida Broberger, Christian |
author_facet | Stagkourakis, Stefanos Pérez, Carolina Thörn Hellysaz, Arash Ammari, Rachida Broberger, Christian |
author_sort | Stagkourakis, Stefanos |
collection | PubMed |
description | Electrical junctions are widespread within the mammalian CNS. Yet, their role in organizing neuronal ensemble activity remains incompletely understood. Here, in a functionally well-characterized system – neuroendocrine tuberoinfundibular dopamine (TIDA) neurons - we demonstrate a striking species difference in network behavior: rat TIDA cells discharge in highly stereotyped, robust, synchronized slow oscillations, whereas mouse oscillations are faster, flexible and show substantial cell-to-cell variability. We show that these distinct operational modes are explained by the presence of strong TIDA-TIDA gap junction coupling in the rat, and its complete absence in the mouse. Both species, however, encompass a similar heterogeneous range of intrinsic resonance frequencies, suggesting similar network building blocks. We demonstrate that gap junctions select and impose the slow network rhythm. These data identify a role for electrical junctions in determining oscillation frequency and show how related species can rely on distinct network strategies to accomplish adaptive control of hormone release. |
format | Online Article Text |
id | pubmed-5933921 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-59339212018-05-07 Network oscillation rules imposed by species-specific electrical coupling Stagkourakis, Stefanos Pérez, Carolina Thörn Hellysaz, Arash Ammari, Rachida Broberger, Christian eLife Neuroscience Electrical junctions are widespread within the mammalian CNS. Yet, their role in organizing neuronal ensemble activity remains incompletely understood. Here, in a functionally well-characterized system – neuroendocrine tuberoinfundibular dopamine (TIDA) neurons - we demonstrate a striking species difference in network behavior: rat TIDA cells discharge in highly stereotyped, robust, synchronized slow oscillations, whereas mouse oscillations are faster, flexible and show substantial cell-to-cell variability. We show that these distinct operational modes are explained by the presence of strong TIDA-TIDA gap junction coupling in the rat, and its complete absence in the mouse. Both species, however, encompass a similar heterogeneous range of intrinsic resonance frequencies, suggesting similar network building blocks. We demonstrate that gap junctions select and impose the slow network rhythm. These data identify a role for electrical junctions in determining oscillation frequency and show how related species can rely on distinct network strategies to accomplish adaptive control of hormone release. eLife Sciences Publications, Ltd 2018-05-03 /pmc/articles/PMC5933921/ /pubmed/29722649 http://dx.doi.org/10.7554/eLife.33144 Text en © 2018, Stagkourakis et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Stagkourakis, Stefanos Pérez, Carolina Thörn Hellysaz, Arash Ammari, Rachida Broberger, Christian Network oscillation rules imposed by species-specific electrical coupling |
title | Network oscillation rules imposed by species-specific electrical coupling |
title_full | Network oscillation rules imposed by species-specific electrical coupling |
title_fullStr | Network oscillation rules imposed by species-specific electrical coupling |
title_full_unstemmed | Network oscillation rules imposed by species-specific electrical coupling |
title_short | Network oscillation rules imposed by species-specific electrical coupling |
title_sort | network oscillation rules imposed by species-specific electrical coupling |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5933921/ https://www.ncbi.nlm.nih.gov/pubmed/29722649 http://dx.doi.org/10.7554/eLife.33144 |
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