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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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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