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Sparsely Distributed, Pre-synaptic Kv3 K(+) Channels Control Spontaneous Firing and Cross-Unit Synchrony via the Regulation of Synaptic Noise in an Auditory Brainstem Circuit

Spontaneous subthreshold activity in the central nervous system is fundamental to information processing and transmission, as it amplifies and optimizes sub-threshold signals, thereby improving action potential initiation and maintaining reliable firing. This form of spontaneous activity, which is f...

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Autores principales: OIsen, Timothy, Capurro, Alberto, Švent, Maša, Pilati, Nadia, Large, Charles, Hartell, Nick, Hamann, Martine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8446535/
https://www.ncbi.nlm.nih.gov/pubmed/34539351
http://dx.doi.org/10.3389/fncel.2021.721371
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author OIsen, Timothy
Capurro, Alberto
Švent, Maša
Pilati, Nadia
Large, Charles
Hartell, Nick
Hamann, Martine
author_facet OIsen, Timothy
Capurro, Alberto
Švent, Maša
Pilati, Nadia
Large, Charles
Hartell, Nick
Hamann, Martine
author_sort OIsen, Timothy
collection PubMed
description Spontaneous subthreshold activity in the central nervous system is fundamental to information processing and transmission, as it amplifies and optimizes sub-threshold signals, thereby improving action potential initiation and maintaining reliable firing. This form of spontaneous activity, which is frequently considered noise, is particularly important at auditory synapses where acoustic information is encoded by rapid and temporally precise firing rates. In contrast, when present in excess, this form of noise becomes detrimental to acoustic information as it contributes to the generation and maintenance of auditory disorders such as tinnitus. The most prominent contribution to subthreshold noise is spontaneous synaptic transmission (synaptic noise). Although numerous studies have examined the role of synaptic noise on single cell excitability, little is known about its pre-synaptic modulation owing in part to the difficulties of combining noise modulation with monitoring synaptic release. Here we study synaptic noise in the auditory brainstem dorsal cochlear nucleus (DCN) of mice and show that pharmacological potentiation of Kv3 K(+) currents reduces the level of synaptic bombardment onto DCN principal fusiform cells. Using a transgenic mouse line (SyG37) expressing SyGCaMP2-mCherry, a calcium sensor that targets pre-synaptic terminals, we show that positive Kv3 K(+) current modulation decreases calcium influx in a fifth of pre-synaptic boutons. Furthermore, while maintaining rapid and precise spike timing, positive Kv3 K(+) current modulation increases the synchronization of local circuit neurons by reducing spontaneous activity. In conclusion, our study identifies a unique pre-synaptic mechanism which reduces synaptic noise at auditory synapses and contributes to the coherent activation of neurons in a local auditory brainstem circuit. This form of modulation highlights a new therapeutic target, namely the pre-synaptic bouton, for ameliorating the effects of hearing disorders which are dependent on aberrant spontaneous activity within the central auditory system.
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spelling pubmed-84465352021-09-18 Sparsely Distributed, Pre-synaptic Kv3 K(+) Channels Control Spontaneous Firing and Cross-Unit Synchrony via the Regulation of Synaptic Noise in an Auditory Brainstem Circuit OIsen, Timothy Capurro, Alberto Švent, Maša Pilati, Nadia Large, Charles Hartell, Nick Hamann, Martine Front Cell Neurosci Neuroscience Spontaneous subthreshold activity in the central nervous system is fundamental to information processing and transmission, as it amplifies and optimizes sub-threshold signals, thereby improving action potential initiation and maintaining reliable firing. This form of spontaneous activity, which is frequently considered noise, is particularly important at auditory synapses where acoustic information is encoded by rapid and temporally precise firing rates. In contrast, when present in excess, this form of noise becomes detrimental to acoustic information as it contributes to the generation and maintenance of auditory disorders such as tinnitus. The most prominent contribution to subthreshold noise is spontaneous synaptic transmission (synaptic noise). Although numerous studies have examined the role of synaptic noise on single cell excitability, little is known about its pre-synaptic modulation owing in part to the difficulties of combining noise modulation with monitoring synaptic release. Here we study synaptic noise in the auditory brainstem dorsal cochlear nucleus (DCN) of mice and show that pharmacological potentiation of Kv3 K(+) currents reduces the level of synaptic bombardment onto DCN principal fusiform cells. Using a transgenic mouse line (SyG37) expressing SyGCaMP2-mCherry, a calcium sensor that targets pre-synaptic terminals, we show that positive Kv3 K(+) current modulation decreases calcium influx in a fifth of pre-synaptic boutons. Furthermore, while maintaining rapid and precise spike timing, positive Kv3 K(+) current modulation increases the synchronization of local circuit neurons by reducing spontaneous activity. In conclusion, our study identifies a unique pre-synaptic mechanism which reduces synaptic noise at auditory synapses and contributes to the coherent activation of neurons in a local auditory brainstem circuit. This form of modulation highlights a new therapeutic target, namely the pre-synaptic bouton, for ameliorating the effects of hearing disorders which are dependent on aberrant spontaneous activity within the central auditory system. Frontiers Media S.A. 2021-09-03 /pmc/articles/PMC8446535/ /pubmed/34539351 http://dx.doi.org/10.3389/fncel.2021.721371 Text en Copyright © 2021 OIsen, Capurro, Švent, Pilati, Large, Hartell and Hamann. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
OIsen, Timothy
Capurro, Alberto
Švent, Maša
Pilati, Nadia
Large, Charles
Hartell, Nick
Hamann, Martine
Sparsely Distributed, Pre-synaptic Kv3 K(+) Channels Control Spontaneous Firing and Cross-Unit Synchrony via the Regulation of Synaptic Noise in an Auditory Brainstem Circuit
title Sparsely Distributed, Pre-synaptic Kv3 K(+) Channels Control Spontaneous Firing and Cross-Unit Synchrony via the Regulation of Synaptic Noise in an Auditory Brainstem Circuit
title_full Sparsely Distributed, Pre-synaptic Kv3 K(+) Channels Control Spontaneous Firing and Cross-Unit Synchrony via the Regulation of Synaptic Noise in an Auditory Brainstem Circuit
title_fullStr Sparsely Distributed, Pre-synaptic Kv3 K(+) Channels Control Spontaneous Firing and Cross-Unit Synchrony via the Regulation of Synaptic Noise in an Auditory Brainstem Circuit
title_full_unstemmed Sparsely Distributed, Pre-synaptic Kv3 K(+) Channels Control Spontaneous Firing and Cross-Unit Synchrony via the Regulation of Synaptic Noise in an Auditory Brainstem Circuit
title_short Sparsely Distributed, Pre-synaptic Kv3 K(+) Channels Control Spontaneous Firing and Cross-Unit Synchrony via the Regulation of Synaptic Noise in an Auditory Brainstem Circuit
title_sort sparsely distributed, pre-synaptic kv3 k(+) channels control spontaneous firing and cross-unit synchrony via the regulation of synaptic noise in an auditory brainstem circuit
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8446535/
https://www.ncbi.nlm.nih.gov/pubmed/34539351
http://dx.doi.org/10.3389/fncel.2021.721371
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