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Sensory input drives rapid homeostatic scaling of the axon initial segment in mouse barrel cortex

The axon initial segment (AIS) is a critical microdomain for action potential initiation and implicated in the regulation of neuronal excitability during activity-dependent plasticity. While structural AIS plasticity has been suggested to fine-tune neuronal activity when network states change, wheth...

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Autores principales: Jamann, Nora, Dannehl, Dominik, Lehmann, Nadja, Wagener, Robin, Thielemann, Corinna, Schultz, Christian, Staiger, Jochen, Kole, Maarten H. P., Engelhardt, Maren
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7782484/
https://www.ncbi.nlm.nih.gov/pubmed/33397944
http://dx.doi.org/10.1038/s41467-020-20232-x
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author Jamann, Nora
Dannehl, Dominik
Lehmann, Nadja
Wagener, Robin
Thielemann, Corinna
Schultz, Christian
Staiger, Jochen
Kole, Maarten H. P.
Engelhardt, Maren
author_facet Jamann, Nora
Dannehl, Dominik
Lehmann, Nadja
Wagener, Robin
Thielemann, Corinna
Schultz, Christian
Staiger, Jochen
Kole, Maarten H. P.
Engelhardt, Maren
author_sort Jamann, Nora
collection PubMed
description The axon initial segment (AIS) is a critical microdomain for action potential initiation and implicated in the regulation of neuronal excitability during activity-dependent plasticity. While structural AIS plasticity has been suggested to fine-tune neuronal activity when network states change, whether it acts in vivo as a homeostatic regulatory mechanism in behaviorally relevant contexts remains poorly understood. Using the mouse whisker-to-barrel pathway as a model system in combination with immunofluorescence, confocal analysis and electrophysiological recordings, we observed bidirectional AIS plasticity in cortical pyramidal neurons. Furthermore, we find that structural and functional AIS remodeling occurs in distinct temporal domains: Long-term sensory deprivation elicits an AIS length increase, accompanied with an increase in neuronal excitability, while sensory enrichment results in a rapid AIS shortening, accompanied by a decrease in action potential generation. Our findings highlight a central role of the AIS in the homeostatic regulation of neuronal input-output relations.
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spelling pubmed-77824842021-01-11 Sensory input drives rapid homeostatic scaling of the axon initial segment in mouse barrel cortex Jamann, Nora Dannehl, Dominik Lehmann, Nadja Wagener, Robin Thielemann, Corinna Schultz, Christian Staiger, Jochen Kole, Maarten H. P. Engelhardt, Maren Nat Commun Article The axon initial segment (AIS) is a critical microdomain for action potential initiation and implicated in the regulation of neuronal excitability during activity-dependent plasticity. While structural AIS plasticity has been suggested to fine-tune neuronal activity when network states change, whether it acts in vivo as a homeostatic regulatory mechanism in behaviorally relevant contexts remains poorly understood. Using the mouse whisker-to-barrel pathway as a model system in combination with immunofluorescence, confocal analysis and electrophysiological recordings, we observed bidirectional AIS plasticity in cortical pyramidal neurons. Furthermore, we find that structural and functional AIS remodeling occurs in distinct temporal domains: Long-term sensory deprivation elicits an AIS length increase, accompanied with an increase in neuronal excitability, while sensory enrichment results in a rapid AIS shortening, accompanied by a decrease in action potential generation. Our findings highlight a central role of the AIS in the homeostatic regulation of neuronal input-output relations. Nature Publishing Group UK 2021-01-04 /pmc/articles/PMC7782484/ /pubmed/33397944 http://dx.doi.org/10.1038/s41467-020-20232-x Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Jamann, Nora
Dannehl, Dominik
Lehmann, Nadja
Wagener, Robin
Thielemann, Corinna
Schultz, Christian
Staiger, Jochen
Kole, Maarten H. P.
Engelhardt, Maren
Sensory input drives rapid homeostatic scaling of the axon initial segment in mouse barrel cortex
title Sensory input drives rapid homeostatic scaling of the axon initial segment in mouse barrel cortex
title_full Sensory input drives rapid homeostatic scaling of the axon initial segment in mouse barrel cortex
title_fullStr Sensory input drives rapid homeostatic scaling of the axon initial segment in mouse barrel cortex
title_full_unstemmed Sensory input drives rapid homeostatic scaling of the axon initial segment in mouse barrel cortex
title_short Sensory input drives rapid homeostatic scaling of the axon initial segment in mouse barrel cortex
title_sort sensory input drives rapid homeostatic scaling of the axon initial segment in mouse barrel cortex
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7782484/
https://www.ncbi.nlm.nih.gov/pubmed/33397944
http://dx.doi.org/10.1038/s41467-020-20232-x
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