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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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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. |
format | Online Article Text |
id | pubmed-7782484 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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