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Large, Stable Spikes Exhibit Differential Broadening in Excitatory and Inhibitory Neocortical Boutons
Presynaptic action potential spikes control neurotransmitter release and thus interneuronal communication. However, the properties and the dynamics of presynaptic spikes in the neocortex remain enigmatic because boutons in the neocortex are small and direct patch-clamp recordings have not been perfo...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7809622/ https://www.ncbi.nlm.nih.gov/pubmed/33440142 http://dx.doi.org/10.1016/j.celrep.2020.108612 |
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author | Ritzau-Jost, Andreas Tsintsadze, Timur Krueger, Martin Ader, Jonas Bechmann, Ingo Eilers, Jens Barbour, Boris Smith, Stephen M. Hallermann, Stefan |
author_facet | Ritzau-Jost, Andreas Tsintsadze, Timur Krueger, Martin Ader, Jonas Bechmann, Ingo Eilers, Jens Barbour, Boris Smith, Stephen M. Hallermann, Stefan |
author_sort | Ritzau-Jost, Andreas |
collection | PubMed |
description | Presynaptic action potential spikes control neurotransmitter release and thus interneuronal communication. However, the properties and the dynamics of presynaptic spikes in the neocortex remain enigmatic because boutons in the neocortex are small and direct patch-clamp recordings have not been performed. Here, we report direct recordings from boutons of neocortical pyramidal neurons and interneurons. Our data reveal rapid and large presynaptic action potentials in layer 5 neurons and fast-spiking interneurons reliably propagating into axon collaterals. For in-depth analyses, we establish boutons of mature cultured neurons as models for excitatory neocortical boutons, demonstrating that the presynaptic spike amplitude is unaffected by potassium channels, homeostatic long-term plasticity, and high-frequency firing. In contrast to the stable amplitude, presynaptic spikes profoundly broaden during high-frequency firing in layer 5 pyramidal neurons, but not in fast-spiking interneurons. Thus, our data demonstrate large presynaptic spikes and fundamental differences between excitatory and inhibitory boutons in the neocortex. |
format | Online Article Text |
id | pubmed-7809622 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-78096222021-01-22 Large, Stable Spikes Exhibit Differential Broadening in Excitatory and Inhibitory Neocortical Boutons Ritzau-Jost, Andreas Tsintsadze, Timur Krueger, Martin Ader, Jonas Bechmann, Ingo Eilers, Jens Barbour, Boris Smith, Stephen M. Hallermann, Stefan Cell Rep Article Presynaptic action potential spikes control neurotransmitter release and thus interneuronal communication. However, the properties and the dynamics of presynaptic spikes in the neocortex remain enigmatic because boutons in the neocortex are small and direct patch-clamp recordings have not been performed. Here, we report direct recordings from boutons of neocortical pyramidal neurons and interneurons. Our data reveal rapid and large presynaptic action potentials in layer 5 neurons and fast-spiking interneurons reliably propagating into axon collaterals. For in-depth analyses, we establish boutons of mature cultured neurons as models for excitatory neocortical boutons, demonstrating that the presynaptic spike amplitude is unaffected by potassium channels, homeostatic long-term plasticity, and high-frequency firing. In contrast to the stable amplitude, presynaptic spikes profoundly broaden during high-frequency firing in layer 5 pyramidal neurons, but not in fast-spiking interneurons. Thus, our data demonstrate large presynaptic spikes and fundamental differences between excitatory and inhibitory boutons in the neocortex. Cell Press 2021-01-12 /pmc/articles/PMC7809622/ /pubmed/33440142 http://dx.doi.org/10.1016/j.celrep.2020.108612 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Ritzau-Jost, Andreas Tsintsadze, Timur Krueger, Martin Ader, Jonas Bechmann, Ingo Eilers, Jens Barbour, Boris Smith, Stephen M. Hallermann, Stefan Large, Stable Spikes Exhibit Differential Broadening in Excitatory and Inhibitory Neocortical Boutons |
title | Large, Stable Spikes Exhibit Differential Broadening in Excitatory and Inhibitory Neocortical Boutons |
title_full | Large, Stable Spikes Exhibit Differential Broadening in Excitatory and Inhibitory Neocortical Boutons |
title_fullStr | Large, Stable Spikes Exhibit Differential Broadening in Excitatory and Inhibitory Neocortical Boutons |
title_full_unstemmed | Large, Stable Spikes Exhibit Differential Broadening in Excitatory and Inhibitory Neocortical Boutons |
title_short | Large, Stable Spikes Exhibit Differential Broadening in Excitatory and Inhibitory Neocortical Boutons |
title_sort | large, stable spikes exhibit differential broadening in excitatory and inhibitory neocortical boutons |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7809622/ https://www.ncbi.nlm.nih.gov/pubmed/33440142 http://dx.doi.org/10.1016/j.celrep.2020.108612 |
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