Plasticity of GABAA receptor diffusion dynamics at the axon initial segment
The axon initial segment (AIS), a site of action potential initiation, undergoes activity-dependent homeostatic repositioning to fine-tune neuronal activity. However, little is known about the behaviour of GABAA receptors (GABAARs) at synapses made onto the axon and especially the AIS. Here, we stud...
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doaj-b594d8e1334e451a9eab2d91e53703e42020-11-24T21:01:27ZengFrontiers Media S.A.Frontiers in Cellular Neuroscience1662-51022014-06-01810.3389/fncel.2014.0015182329Plasticity of GABAA receptor diffusion dynamics at the axon initial segmentJames eMuir0Josef eKittler1University College LondonUniversity College LondonThe axon initial segment (AIS), a site of action potential initiation, undergoes activity-dependent homeostatic repositioning to fine-tune neuronal activity. However, little is known about the behaviour of GABAA receptors (GABAARs) at synapses made onto the axon and especially the AIS. Here, we study the clustering and lateral diffusion of GABAARs in the AIS under baseline conditions, and find that GABAAR lateral mobility is lower in the AIS than dendrites. We find differences in axonal clustering and lateral mobility between GABAARs containing the α1 or α2 subunits, which are known to localize differentially to the AIS. Interestingly, we find that chronic activity driving AIS repositioning does not alter GABAergic synapse location along the axon, but decreases GABAAR cluster size at the AIS. Moreover, in response to chronic depolarization, GABAAR diffusion is strikingly increased in the AIS, and not in dendrites, and this is coupled with a decrease in synaptic residency time of GABAARs at the AIS. We also demonstrate that activation of L-type voltage-gated calcium channels is important for regulating GABAAR lateral mobility at the AIS during chronic depolarization. Modulation of GABAAR diffusion dynamics at the AIS in response to prolonged activity may be a novel mechanism for regulating GABAergic control of information processing.http://journal.frontiersin.org/Journal/10.3389/fncel.2014.00151/fullCalciumDiffusionhomeostatic plasticityaxon initial segmentgaba receptorsQuantum dots |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
James eMuir Josef eKittler |
spellingShingle |
James eMuir Josef eKittler Plasticity of GABAA receptor diffusion dynamics at the axon initial segment Frontiers in Cellular Neuroscience Calcium Diffusion homeostatic plasticity axon initial segment gaba receptors Quantum dots |
author_facet |
James eMuir Josef eKittler |
author_sort |
James eMuir |
title |
Plasticity of GABAA receptor diffusion dynamics at the axon initial segment |
title_short |
Plasticity of GABAA receptor diffusion dynamics at the axon initial segment |
title_full |
Plasticity of GABAA receptor diffusion dynamics at the axon initial segment |
title_fullStr |
Plasticity of GABAA receptor diffusion dynamics at the axon initial segment |
title_full_unstemmed |
Plasticity of GABAA receptor diffusion dynamics at the axon initial segment |
title_sort |
plasticity of gabaa receptor diffusion dynamics at the axon initial segment |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Cellular Neuroscience |
issn |
1662-5102 |
publishDate |
2014-06-01 |
description |
The axon initial segment (AIS), a site of action potential initiation, undergoes activity-dependent homeostatic repositioning to fine-tune neuronal activity. However, little is known about the behaviour of GABAA receptors (GABAARs) at synapses made onto the axon and especially the AIS. Here, we study the clustering and lateral diffusion of GABAARs in the AIS under baseline conditions, and find that GABAAR lateral mobility is lower in the AIS than dendrites. We find differences in axonal clustering and lateral mobility between GABAARs containing the α1 or α2 subunits, which are known to localize differentially to the AIS. Interestingly, we find that chronic activity driving AIS repositioning does not alter GABAergic synapse location along the axon, but decreases GABAAR cluster size at the AIS. Moreover, in response to chronic depolarization, GABAAR diffusion is strikingly increased in the AIS, and not in dendrites, and this is coupled with a decrease in synaptic residency time of GABAARs at the AIS. We also demonstrate that activation of L-type voltage-gated calcium channels is important for regulating GABAAR lateral mobility at the AIS during chronic depolarization. Modulation of GABAAR diffusion dynamics at the AIS in response to prolonged activity may be a novel mechanism for regulating GABAergic control of information processing. |
topic |
Calcium Diffusion homeostatic plasticity axon initial segment gaba receptors Quantum dots |
url |
http://journal.frontiersin.org/Journal/10.3389/fncel.2014.00151/full |
work_keys_str_mv |
AT jamesemuir plasticityofgabaareceptordiffusiondynamicsattheaxoninitialsegment AT josefekittler plasticityofgabaareceptordiffusiondynamicsattheaxoninitialsegment |
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1716777975319363584 |