Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Steinecke, André, Bolton, McLean M., Taniguchi, Hiroki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2022
Materias:
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
_version_ 1784665457686478848
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
work_keys_str_mv AT steineckeandre neuromodulatorycontrolofinhibitorynetworkarborizationinthedevelopingpostnatalneocortex
AT boltonmcleanm neuromodulatorycontrolofinhibitorynetworkarborizationinthedevelopingpostnatalneocortex
AT taniguchihiroki neuromodulatorycontrolofinhibitorynetworkarborizationinthedevelopingpostnatalneocortex