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Simultaneous dendritic voltage and calcium imaging and somatic recording from Purkinje neurons in awake mice

Spatiotemporal maps of dendritic signalling and their relationship with somatic output is fundamental to neuronal information processing, yet remain unexplored in awake animals. Here, we combine simultaneous sub-millisecond voltage and calcium two-photon imaging from distal spiny dendrites, with som...

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Autores principales: Roome, Christopher J., Kuhn, Bernd
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6107665/
https://www.ncbi.nlm.nih.gov/pubmed/30139936
http://dx.doi.org/10.1038/s41467-018-05900-3
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author Roome, Christopher J.
Kuhn, Bernd
author_facet Roome, Christopher J.
Kuhn, Bernd
author_sort Roome, Christopher J.
collection PubMed
description Spatiotemporal maps of dendritic signalling and their relationship with somatic output is fundamental to neuronal information processing, yet remain unexplored in awake animals. Here, we combine simultaneous sub-millisecond voltage and calcium two-photon imaging from distal spiny dendrites, with somatic electrical recording from spontaneously active cerebellar Purkinje neurons (PN) in awake mice. We detect discrete 1−2 ms suprathreshold voltage spikelets in the distal spiny dendrites during dendritic complex spikes. Spikelets and their calcium correlates are highly heterogeneous in number, timing and spatial distribution within and between complex spikes. Back-propagating simple spikes are highly attenuated. Highly variable 5–10 ms voltage hotspots are localized to fine dendritic processes and are reduced in size and frequency by lidocaine and CNQX. Hotspots correlated with somatic output but also, at high frequency, trigger purely dendritic calcium spikes. Summarizing, spatiotemporal signalling in PNs is far more complex, dynamic, and fine scaled than anticipated, even in resting animals.
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spelling pubmed-61076652018-08-27 Simultaneous dendritic voltage and calcium imaging and somatic recording from Purkinje neurons in awake mice Roome, Christopher J. Kuhn, Bernd Nat Commun Article Spatiotemporal maps of dendritic signalling and their relationship with somatic output is fundamental to neuronal information processing, yet remain unexplored in awake animals. Here, we combine simultaneous sub-millisecond voltage and calcium two-photon imaging from distal spiny dendrites, with somatic electrical recording from spontaneously active cerebellar Purkinje neurons (PN) in awake mice. We detect discrete 1−2 ms suprathreshold voltage spikelets in the distal spiny dendrites during dendritic complex spikes. Spikelets and their calcium correlates are highly heterogeneous in number, timing and spatial distribution within and between complex spikes. Back-propagating simple spikes are highly attenuated. Highly variable 5–10 ms voltage hotspots are localized to fine dendritic processes and are reduced in size and frequency by lidocaine and CNQX. Hotspots correlated with somatic output but also, at high frequency, trigger purely dendritic calcium spikes. Summarizing, spatiotemporal signalling in PNs is far more complex, dynamic, and fine scaled than anticipated, even in resting animals. Nature Publishing Group UK 2018-08-23 /pmc/articles/PMC6107665/ /pubmed/30139936 http://dx.doi.org/10.1038/s41467-018-05900-3 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Roome, Christopher J.
Kuhn, Bernd
Simultaneous dendritic voltage and calcium imaging and somatic recording from Purkinje neurons in awake mice
title Simultaneous dendritic voltage and calcium imaging and somatic recording from Purkinje neurons in awake mice
title_full Simultaneous dendritic voltage and calcium imaging and somatic recording from Purkinje neurons in awake mice
title_fullStr Simultaneous dendritic voltage and calcium imaging and somatic recording from Purkinje neurons in awake mice
title_full_unstemmed Simultaneous dendritic voltage and calcium imaging and somatic recording from Purkinje neurons in awake mice
title_short Simultaneous dendritic voltage and calcium imaging and somatic recording from Purkinje neurons in awake mice
title_sort simultaneous dendritic voltage and calcium imaging and somatic recording from purkinje neurons in awake mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6107665/
https://www.ncbi.nlm.nih.gov/pubmed/30139936
http://dx.doi.org/10.1038/s41467-018-05900-3
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