Calcium-Activated Potassium Channels at Nodes of Ranvier Secure Axonal Spike Propagation

Functional connectivity between brain regions relies on long-range signaling by myelinated axons. This is secured by saltatory action potential propagation that depends fundamentally on sodium channel availability at nodes of Ranvier. Although various potassium channel types have been anatomically l...

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Main Authors: Jan Gründemann, Beverley A. Clark
Format: Article
Language:English
Published: Elsevier 2015-09-01
Series:Cell Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2211124715008931
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spelling doaj-61edc0400ed74b14be81f288ef8d1ac92020-11-25T01:39:03ZengElsevierCell Reports2211-12472015-09-0112111715172210.1016/j.celrep.2015.08.022Calcium-Activated Potassium Channels at Nodes of Ranvier Secure Axonal Spike PropagationJan Gründemann0Beverley A. Clark1Wolfson Institute for Biomedical Research, University College London, Gower Street, London WC1E 6BT, UKWolfson Institute for Biomedical Research, University College London, Gower Street, London WC1E 6BT, UKFunctional connectivity between brain regions relies on long-range signaling by myelinated axons. This is secured by saltatory action potential propagation that depends fundamentally on sodium channel availability at nodes of Ranvier. Although various potassium channel types have been anatomically localized to myelinated axons in the brain, direct evidence for their functional recruitment in maintaining node excitability is scarce. Cerebellar Purkinje cells provide continuous input to their targets in the cerebellar nuclei, reliably transmitting axonal spikes over a wide range of rates, requiring a constantly available pool of nodal sodium channels. We show that the recruitment of calcium-activated potassium channels (IK, KCa3.1) by local, activity-dependent calcium (Ca2+) influx at nodes of Ranvier via a T-type voltage-gated Ca2+ current provides a powerful mechanism that likely opposes depolarizing block at the nodes and is thus pivotal to securing continuous axonal spike propagation in spontaneously firing Purkinje cells.http://www.sciencedirect.com/science/article/pii/S2211124715008931
collection DOAJ
language English
format Article
sources DOAJ
author Jan Gründemann
Beverley A. Clark
spellingShingle Jan Gründemann
Beverley A. Clark
Calcium-Activated Potassium Channels at Nodes of Ranvier Secure Axonal Spike Propagation
Cell Reports
author_facet Jan Gründemann
Beverley A. Clark
author_sort Jan Gründemann
title Calcium-Activated Potassium Channels at Nodes of Ranvier Secure Axonal Spike Propagation
title_short Calcium-Activated Potassium Channels at Nodes of Ranvier Secure Axonal Spike Propagation
title_full Calcium-Activated Potassium Channels at Nodes of Ranvier Secure Axonal Spike Propagation
title_fullStr Calcium-Activated Potassium Channels at Nodes of Ranvier Secure Axonal Spike Propagation
title_full_unstemmed Calcium-Activated Potassium Channels at Nodes of Ranvier Secure Axonal Spike Propagation
title_sort calcium-activated potassium channels at nodes of ranvier secure axonal spike propagation
publisher Elsevier
series Cell Reports
issn 2211-1247
publishDate 2015-09-01
description Functional connectivity between brain regions relies on long-range signaling by myelinated axons. This is secured by saltatory action potential propagation that depends fundamentally on sodium channel availability at nodes of Ranvier. Although various potassium channel types have been anatomically localized to myelinated axons in the brain, direct evidence for their functional recruitment in maintaining node excitability is scarce. Cerebellar Purkinje cells provide continuous input to their targets in the cerebellar nuclei, reliably transmitting axonal spikes over a wide range of rates, requiring a constantly available pool of nodal sodium channels. We show that the recruitment of calcium-activated potassium channels (IK, KCa3.1) by local, activity-dependent calcium (Ca2+) influx at nodes of Ranvier via a T-type voltage-gated Ca2+ current provides a powerful mechanism that likely opposes depolarizing block at the nodes and is thus pivotal to securing continuous axonal spike propagation in spontaneously firing Purkinje cells.
url http://www.sciencedirect.com/science/article/pii/S2211124715008931
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AT beverleyaclark calciumactivatedpotassiumchannelsatnodesofranviersecureaxonalspikepropagation
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