Rapid Modulation of Axon Initial Segment Length Influences Repetitive Spike Firing

Neurons implement a variety of plasticity mechanisms to alter their function over timescales ranging from seconds to days. One powerful means of controlling excitability is to directly modulate the site of spike initiation, the axon initial segment (AIS). However, all plastic structural AIS changes...

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Main Authors: Mark D. Evans, Adna S. Dumitrescu, Dennis L.H. Kruijssen, Samuel E. Taylor, Matthew S. Grubb
Format: Article
Language:English
Published: Elsevier 2015-11-01
Series:Cell Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S2211124715011080
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spelling doaj-596be47e16df449e92a56ecdb24a044b2020-11-25T01:49:37ZengElsevierCell Reports2211-12472015-11-011361233124510.1016/j.celrep.2015.09.066Rapid Modulation of Axon Initial Segment Length Influences Repetitive Spike FiringMark D. Evans0Adna S. Dumitrescu1Dennis L.H. Kruijssen2Samuel E. Taylor3Matthew S. Grubb4MRC Centre for Developmental Neurobiology, King’s College London, 4th Floor, New Hunt’s House, Guy’s Campus, London SE1 1UL, UKMRC Centre for Developmental Neurobiology, King’s College London, 4th Floor, New Hunt’s House, Guy’s Campus, London SE1 1UL, UKMRC Centre for Developmental Neurobiology, King’s College London, 4th Floor, New Hunt’s House, Guy’s Campus, London SE1 1UL, UKMRC Centre for Developmental Neurobiology, King’s College London, 4th Floor, New Hunt’s House, Guy’s Campus, London SE1 1UL, UKMRC Centre for Developmental Neurobiology, King’s College London, 4th Floor, New Hunt’s House, Guy’s Campus, London SE1 1UL, UKNeurons implement a variety of plasticity mechanisms to alter their function over timescales ranging from seconds to days. One powerful means of controlling excitability is to directly modulate the site of spike initiation, the axon initial segment (AIS). However, all plastic structural AIS changes reported thus far have been slow, involving days of neuronal activity perturbation. Here, we show that AIS plasticity can be induced much more rapidly. Just 3 hr of elevated activity significantly shortened the AIS of dentate granule cells in a calcineurin-dependent manner. The functional effects of rapid AIS shortening were offset by dephosphorylation of voltage-gated sodium channels, another calcineurin-dependent mechanism. However, pharmacological separation of these phenomena revealed a significant relationship between AIS length and repetitive firing. The AIS can therefore undergo a rapid form of structural change over timescales that enable interactions with other forms of activity-dependent plasticity in the dynamic control of neuronal excitability.http://www.sciencedirect.com/science/article/pii/S2211124715011080
collection DOAJ
language English
format Article
sources DOAJ
author Mark D. Evans
Adna S. Dumitrescu
Dennis L.H. Kruijssen
Samuel E. Taylor
Matthew S. Grubb
spellingShingle Mark D. Evans
Adna S. Dumitrescu
Dennis L.H. Kruijssen
Samuel E. Taylor
Matthew S. Grubb
Rapid Modulation of Axon Initial Segment Length Influences Repetitive Spike Firing
Cell Reports
author_facet Mark D. Evans
Adna S. Dumitrescu
Dennis L.H. Kruijssen
Samuel E. Taylor
Matthew S. Grubb
author_sort Mark D. Evans
title Rapid Modulation of Axon Initial Segment Length Influences Repetitive Spike Firing
title_short Rapid Modulation of Axon Initial Segment Length Influences Repetitive Spike Firing
title_full Rapid Modulation of Axon Initial Segment Length Influences Repetitive Spike Firing
title_fullStr Rapid Modulation of Axon Initial Segment Length Influences Repetitive Spike Firing
title_full_unstemmed Rapid Modulation of Axon Initial Segment Length Influences Repetitive Spike Firing
title_sort rapid modulation of axon initial segment length influences repetitive spike firing
publisher Elsevier
series Cell Reports
issn 2211-1247
publishDate 2015-11-01
description Neurons implement a variety of plasticity mechanisms to alter their function over timescales ranging from seconds to days. One powerful means of controlling excitability is to directly modulate the site of spike initiation, the axon initial segment (AIS). However, all plastic structural AIS changes reported thus far have been slow, involving days of neuronal activity perturbation. Here, we show that AIS plasticity can be induced much more rapidly. Just 3 hr of elevated activity significantly shortened the AIS of dentate granule cells in a calcineurin-dependent manner. The functional effects of rapid AIS shortening were offset by dephosphorylation of voltage-gated sodium channels, another calcineurin-dependent mechanism. However, pharmacological separation of these phenomena revealed a significant relationship between AIS length and repetitive firing. The AIS can therefore undergo a rapid form of structural change over timescales that enable interactions with other forms of activity-dependent plasticity in the dynamic control of neuronal excitability.
url http://www.sciencedirect.com/science/article/pii/S2211124715011080
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