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Signal processing by T-type calcium channel interactions in the cerebellum
T-type calcium channels of the Cav3 family are unique among voltage-gated calcium channels due to their low activation voltage, rapid inactivation, and small single channel conductance. These special properties allow Cav3 calcium channels to regulate neuronal processing in the subthreshold voltage r...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3841819/ https://www.ncbi.nlm.nih.gov/pubmed/24348329 http://dx.doi.org/10.3389/fncel.2013.00230 |
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author | Engbers, Jordan D. T. Anderson, Dustin Zamponi, Gerald W. Turner, Ray W. |
author_facet | Engbers, Jordan D. T. Anderson, Dustin Zamponi, Gerald W. Turner, Ray W. |
author_sort | Engbers, Jordan D. T. |
collection | PubMed |
description | T-type calcium channels of the Cav3 family are unique among voltage-gated calcium channels due to their low activation voltage, rapid inactivation, and small single channel conductance. These special properties allow Cav3 calcium channels to regulate neuronal processing in the subthreshold voltage range. Here, we review two different subthreshold ion channel interactions involving Cav3 channels and explore the ability of these interactions to expand the functional roles of Cav3 channels. In cerebellar Purkinje cells, Cav3 and intermediate conductance calcium-activated potassium (IKCa) channels form a novel complex which creates a low voltage-activated, transient outward current capable of suppressing temporal summation of excitatory postsynaptic potentials (EPSPs). In large diameter neurons of the deep cerebellar nuclei, Cav3-mediated calcium current (I(T)) and hyperpolarization-activated cation current (I(H)) are activated during trains of inhibitory postsynaptic potentials. These currents have distinct, and yet synergistic, roles in the subthreshold domain with I(T) generating a rebound burst and I(H) controlling first spike latency and rebound spike precision. However, by shortening the membrane time constant the membrane returns towards resting value at a faster rate, allowing I(H) to increase the efficacy of I(T) and increase the range of burst frequencies that can be generated. The net effect of Cav3 channels thus depends on the channels with which they are paired. When expressed in a complex with a K(Ca) channel, Cav3 channels reduce excitability when processing excitatory inputs. If functionally coupled with an HCN channel, the depolarizing effect of Cav3 channels is accentuated, allowing for efficient inversion of inhibitory inputs to generate a rebound burst output. Therefore, signal processing relies not only on the activity of individual subtypes of channels but also on complex interactions between ion channels whether based on a physical complex or by indirect effects on membrane properties. |
format | Online Article Text |
id | pubmed-3841819 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-38418192013-12-13 Signal processing by T-type calcium channel interactions in the cerebellum Engbers, Jordan D. T. Anderson, Dustin Zamponi, Gerald W. Turner, Ray W. Front Cell Neurosci Neuroscience T-type calcium channels of the Cav3 family are unique among voltage-gated calcium channels due to their low activation voltage, rapid inactivation, and small single channel conductance. These special properties allow Cav3 calcium channels to regulate neuronal processing in the subthreshold voltage range. Here, we review two different subthreshold ion channel interactions involving Cav3 channels and explore the ability of these interactions to expand the functional roles of Cav3 channels. In cerebellar Purkinje cells, Cav3 and intermediate conductance calcium-activated potassium (IKCa) channels form a novel complex which creates a low voltage-activated, transient outward current capable of suppressing temporal summation of excitatory postsynaptic potentials (EPSPs). In large diameter neurons of the deep cerebellar nuclei, Cav3-mediated calcium current (I(T)) and hyperpolarization-activated cation current (I(H)) are activated during trains of inhibitory postsynaptic potentials. These currents have distinct, and yet synergistic, roles in the subthreshold domain with I(T) generating a rebound burst and I(H) controlling first spike latency and rebound spike precision. However, by shortening the membrane time constant the membrane returns towards resting value at a faster rate, allowing I(H) to increase the efficacy of I(T) and increase the range of burst frequencies that can be generated. The net effect of Cav3 channels thus depends on the channels with which they are paired. When expressed in a complex with a K(Ca) channel, Cav3 channels reduce excitability when processing excitatory inputs. If functionally coupled with an HCN channel, the depolarizing effect of Cav3 channels is accentuated, allowing for efficient inversion of inhibitory inputs to generate a rebound burst output. Therefore, signal processing relies not only on the activity of individual subtypes of channels but also on complex interactions between ion channels whether based on a physical complex or by indirect effects on membrane properties. Frontiers Media S.A. 2013-11-27 /pmc/articles/PMC3841819/ /pubmed/24348329 http://dx.doi.org/10.3389/fncel.2013.00230 Text en Copyright © 2013 Engbers, Anderson, Zamponi and Turner. http://creativecommons.org/licenses/by/3.0/ 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) or licensor 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 Engbers, Jordan D. T. Anderson, Dustin Zamponi, Gerald W. Turner, Ray W. Signal processing by T-type calcium channel interactions in the cerebellum |
title | Signal processing by T-type calcium channel interactions in the cerebellum |
title_full | Signal processing by T-type calcium channel interactions in the cerebellum |
title_fullStr | Signal processing by T-type calcium channel interactions in the cerebellum |
title_full_unstemmed | Signal processing by T-type calcium channel interactions in the cerebellum |
title_short | Signal processing by T-type calcium channel interactions in the cerebellum |
title_sort | signal processing by t-type calcium channel interactions in the cerebellum |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3841819/ https://www.ncbi.nlm.nih.gov/pubmed/24348329 http://dx.doi.org/10.3389/fncel.2013.00230 |
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