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Neuromodulatory control of inhibitory network arborization in the developing postnatal neocortex
Interregional neuronal communication is pivotal to instructing and adjusting cortical circuit assembly. Subcortical neuromodulatory systems project long-range axons to the cortex and affect cortical processing. However, their roles and signaling mechanisms in cortical wiring remain poorly understood...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8906727/ https://www.ncbi.nlm.nih.gov/pubmed/35263136 http://dx.doi.org/10.1126/sciadv.abe7192 |
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author | Steinecke, André Bolton, McLean M. Taniguchi, Hiroki |
author_facet | Steinecke, André Bolton, McLean M. Taniguchi, Hiroki |
author_sort | Steinecke, André |
collection | PubMed |
description | Interregional neuronal communication is pivotal to instructing and adjusting cortical circuit assembly. Subcortical neuromodulatory systems project long-range axons to the cortex and affect cortical processing. However, their roles and signaling mechanisms in cortical wiring remain poorly understood. Here, we explored whether and how the cholinergic system regulates inhibitory axonal ramification of neocortical chandelier cells (ChCs), which control spike generation by innervating axon initial segments of pyramidal neurons. We found that acetylcholine (ACh) signaling through nicotinic ACh receptors (nAChRs) and downstream T-type voltage-dependent calcium (Ca(2+)) channels cell-autonomously controls axonal arborization in developing ChCs through regulating filopodia initiation. This signaling axis shapes the basal Ca(2+) level range in varicosities where filopodia originate. Furthermore, the normal development of ChC axonal arbors requires proper levels of activity in subcortical cholinergic neurons. Thus, the cholinergic system regulates inhibitory network arborization in the developing neocortex and may tune cortical circuit properties depending on early-life experiences. |
format | Online Article Text |
id | pubmed-8906727 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-89067272022-03-21 Neuromodulatory control of inhibitory network arborization in the developing postnatal neocortex Steinecke, André Bolton, McLean M. Taniguchi, Hiroki Sci Adv Neuroscience Interregional neuronal communication is pivotal to instructing and adjusting cortical circuit assembly. Subcortical neuromodulatory systems project long-range axons to the cortex and affect cortical processing. However, their roles and signaling mechanisms in cortical wiring remain poorly understood. Here, we explored whether and how the cholinergic system regulates inhibitory axonal ramification of neocortical chandelier cells (ChCs), which control spike generation by innervating axon initial segments of pyramidal neurons. We found that acetylcholine (ACh) signaling through nicotinic ACh receptors (nAChRs) and downstream T-type voltage-dependent calcium (Ca(2+)) channels cell-autonomously controls axonal arborization in developing ChCs through regulating filopodia initiation. This signaling axis shapes the basal Ca(2+) level range in varicosities where filopodia originate. Furthermore, the normal development of ChC axonal arbors requires proper levels of activity in subcortical cholinergic neurons. Thus, the cholinergic system regulates inhibitory network arborization in the developing neocortex and may tune cortical circuit properties depending on early-life experiences. American Association for the Advancement of Science 2022-03-09 /pmc/articles/PMC8906727/ /pubmed/35263136 http://dx.doi.org/10.1126/sciadv.abe7192 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Neuroscience Steinecke, André Bolton, McLean M. Taniguchi, Hiroki Neuromodulatory control of inhibitory network arborization in the developing postnatal neocortex |
title | Neuromodulatory control of inhibitory network arborization in the developing postnatal neocortex |
title_full | Neuromodulatory control of inhibitory network arborization in the developing postnatal neocortex |
title_fullStr | Neuromodulatory control of inhibitory network arborization in the developing postnatal neocortex |
title_full_unstemmed | Neuromodulatory control of inhibitory network arborization in the developing postnatal neocortex |
title_short | Neuromodulatory control of inhibitory network arborization in the developing postnatal neocortex |
title_sort | neuromodulatory control of inhibitory network arborization in the developing postnatal neocortex |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8906727/ https://www.ncbi.nlm.nih.gov/pubmed/35263136 http://dx.doi.org/10.1126/sciadv.abe7192 |
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