Cargando…

The subthreshold-active K(V)7 current regulates neurotransmission by limiting spike-induced Ca(2+) influx in hippocampal mossy fiber synaptic terminals

Little is known about the properties and function of ion channels that affect synaptic terminal-resting properties. One particular subthreshold-active ion channel, the Kv7 potassium channel, is highly localized to axons, but its role in regulating synaptic terminal intrinsic excitability and release...

Descripción completa

Detalles Bibliográficos
Autores principales: Martinello, Katiuscia, Giacalone, Elisabetta, Migliore, Michele, Brown, David A., Shah, Mala M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6486593/
https://www.ncbi.nlm.nih.gov/pubmed/31044170
http://dx.doi.org/10.1038/s42003-019-0408-4
_version_ 1783414368447234048
author Martinello, Katiuscia
Giacalone, Elisabetta
Migliore, Michele
Brown, David A.
Shah, Mala M.
author_facet Martinello, Katiuscia
Giacalone, Elisabetta
Migliore, Michele
Brown, David A.
Shah, Mala M.
author_sort Martinello, Katiuscia
collection PubMed
description Little is known about the properties and function of ion channels that affect synaptic terminal-resting properties. One particular subthreshold-active ion channel, the Kv7 potassium channel, is highly localized to axons, but its role in regulating synaptic terminal intrinsic excitability and release is largely unexplored. Using electrophysiological recordings together with computational modeling, we found that the K(V)7 current was active at rest in adult hippocampal mossy fiber synaptic terminals and enhanced their membrane conductance. The current also restrained action potential-induced Ca(2+) influx via N- and P/Q-type Ca(2+) channels in boutons. This was associated with a substantial reduction in the spike half-width and afterdepolarization following presynaptic spikes. Further, by constraining spike-induced Ca(2+) influx, the presynaptic K(V)7 current decreased neurotransmission onto CA3 pyramidal neurons and short-term synaptic plasticity at the mossy fiber–CA3 synapse. This is a distinctive mechanism by which K(V)7 channels influence hippocampal neuronal excitability and synaptic plasticity.
format Online
Article
Text
id pubmed-6486593
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-64865932019-05-01 The subthreshold-active K(V)7 current regulates neurotransmission by limiting spike-induced Ca(2+) influx in hippocampal mossy fiber synaptic terminals Martinello, Katiuscia Giacalone, Elisabetta Migliore, Michele Brown, David A. Shah, Mala M. Commun Biol Article Little is known about the properties and function of ion channels that affect synaptic terminal-resting properties. One particular subthreshold-active ion channel, the Kv7 potassium channel, is highly localized to axons, but its role in regulating synaptic terminal intrinsic excitability and release is largely unexplored. Using electrophysiological recordings together with computational modeling, we found that the K(V)7 current was active at rest in adult hippocampal mossy fiber synaptic terminals and enhanced their membrane conductance. The current also restrained action potential-induced Ca(2+) influx via N- and P/Q-type Ca(2+) channels in boutons. This was associated with a substantial reduction in the spike half-width and afterdepolarization following presynaptic spikes. Further, by constraining spike-induced Ca(2+) influx, the presynaptic K(V)7 current decreased neurotransmission onto CA3 pyramidal neurons and short-term synaptic plasticity at the mossy fiber–CA3 synapse. This is a distinctive mechanism by which K(V)7 channels influence hippocampal neuronal excitability and synaptic plasticity. Nature Publishing Group UK 2019-04-26 /pmc/articles/PMC6486593/ /pubmed/31044170 http://dx.doi.org/10.1038/s42003-019-0408-4 Text en © The Author(s) 2019 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
Martinello, Katiuscia
Giacalone, Elisabetta
Migliore, Michele
Brown, David A.
Shah, Mala M.
The subthreshold-active K(V)7 current regulates neurotransmission by limiting spike-induced Ca(2+) influx in hippocampal mossy fiber synaptic terminals
title The subthreshold-active K(V)7 current regulates neurotransmission by limiting spike-induced Ca(2+) influx in hippocampal mossy fiber synaptic terminals
title_full The subthreshold-active K(V)7 current regulates neurotransmission by limiting spike-induced Ca(2+) influx in hippocampal mossy fiber synaptic terminals
title_fullStr The subthreshold-active K(V)7 current regulates neurotransmission by limiting spike-induced Ca(2+) influx in hippocampal mossy fiber synaptic terminals
title_full_unstemmed The subthreshold-active K(V)7 current regulates neurotransmission by limiting spike-induced Ca(2+) influx in hippocampal mossy fiber synaptic terminals
title_short The subthreshold-active K(V)7 current regulates neurotransmission by limiting spike-induced Ca(2+) influx in hippocampal mossy fiber synaptic terminals
title_sort subthreshold-active k(v)7 current regulates neurotransmission by limiting spike-induced ca(2+) influx in hippocampal mossy fiber synaptic terminals
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6486593/
https://www.ncbi.nlm.nih.gov/pubmed/31044170
http://dx.doi.org/10.1038/s42003-019-0408-4
work_keys_str_mv AT martinellokatiuscia thesubthresholdactivekv7currentregulatesneurotransmissionbylimitingspikeinducedca2influxinhippocampalmossyfibersynapticterminals
AT giacaloneelisabetta thesubthresholdactivekv7currentregulatesneurotransmissionbylimitingspikeinducedca2influxinhippocampalmossyfibersynapticterminals
AT miglioremichele thesubthresholdactivekv7currentregulatesneurotransmissionbylimitingspikeinducedca2influxinhippocampalmossyfibersynapticterminals
AT browndavida thesubthresholdactivekv7currentregulatesneurotransmissionbylimitingspikeinducedca2influxinhippocampalmossyfibersynapticterminals
AT shahmalam thesubthresholdactivekv7currentregulatesneurotransmissionbylimitingspikeinducedca2influxinhippocampalmossyfibersynapticterminals
AT martinellokatiuscia subthresholdactivekv7currentregulatesneurotransmissionbylimitingspikeinducedca2influxinhippocampalmossyfibersynapticterminals
AT giacaloneelisabetta subthresholdactivekv7currentregulatesneurotransmissionbylimitingspikeinducedca2influxinhippocampalmossyfibersynapticterminals
AT miglioremichele subthresholdactivekv7currentregulatesneurotransmissionbylimitingspikeinducedca2influxinhippocampalmossyfibersynapticterminals
AT browndavida subthresholdactivekv7currentregulatesneurotransmissionbylimitingspikeinducedca2influxinhippocampalmossyfibersynapticterminals
AT shahmalam subthresholdactivekv7currentregulatesneurotransmissionbylimitingspikeinducedca2influxinhippocampalmossyfibersynapticterminals