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Somato-dendritic decoupling as a novel mechanism for protracted cortical maturation

BACKGROUND: Both human and animal data indicate that disruption of the endogenously slow maturation of temporal association cortical (TeA) networks is associated with abnormal higher order cognitive development. However, the neuronal mechanisms underlying the endogenous maturation delay of the TeA a...

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Autores principales: Chomiak, Taylor, Hung, Johanna, Nguyen, Minh Dang, Hu, Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4916537/
https://www.ncbi.nlm.nih.gov/pubmed/27328836
http://dx.doi.org/10.1186/s12915-016-0270-5
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author Chomiak, Taylor
Hung, Johanna
Nguyen, Minh Dang
Hu, Bin
author_facet Chomiak, Taylor
Hung, Johanna
Nguyen, Minh Dang
Hu, Bin
author_sort Chomiak, Taylor
collection PubMed
description BACKGROUND: Both human and animal data indicate that disruption of the endogenously slow maturation of temporal association cortical (TeA) networks is associated with abnormal higher order cognitive development. However, the neuronal mechanisms underlying the endogenous maturation delay of the TeA are poorly understood. RESULTS: Here we report a novel form of developmental plasticity that is present in the TeA. It was found that deep layer TeA neurons, but not hippocampal or primary visual neurons, exist in a protracted ’embryonic-like’ state through a mechanism involving reduced somato-dendritic communication and a non-excitable somatic membrane. This mechanism of neural inactivity is present in intact tissue and shows a remarkable transition into an active somato-dendritically coupled state. The quantity of decoupled cells diminishes in a protracted and age-dependent manner, continuing into adolescence. CONCLUSIONS: Based on our data, we propose a model of neural plasticity through which protracted compartmentalization and decoupling in somato-dendritic signalling plays a key role in controlling how excitable neurons are incorporated into recurrent cortical networks independent of neurogenesis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12915-016-0270-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-49165372016-06-23 Somato-dendritic decoupling as a novel mechanism for protracted cortical maturation Chomiak, Taylor Hung, Johanna Nguyen, Minh Dang Hu, Bin BMC Biol Research Article BACKGROUND: Both human and animal data indicate that disruption of the endogenously slow maturation of temporal association cortical (TeA) networks is associated with abnormal higher order cognitive development. However, the neuronal mechanisms underlying the endogenous maturation delay of the TeA are poorly understood. RESULTS: Here we report a novel form of developmental plasticity that is present in the TeA. It was found that deep layer TeA neurons, but not hippocampal or primary visual neurons, exist in a protracted ’embryonic-like’ state through a mechanism involving reduced somato-dendritic communication and a non-excitable somatic membrane. This mechanism of neural inactivity is present in intact tissue and shows a remarkable transition into an active somato-dendritically coupled state. The quantity of decoupled cells diminishes in a protracted and age-dependent manner, continuing into adolescence. CONCLUSIONS: Based on our data, we propose a model of neural plasticity through which protracted compartmentalization and decoupling in somato-dendritic signalling plays a key role in controlling how excitable neurons are incorporated into recurrent cortical networks independent of neurogenesis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12915-016-0270-5) contains supplementary material, which is available to authorized users. BioMed Central 2016-06-21 /pmc/articles/PMC4916537/ /pubmed/27328836 http://dx.doi.org/10.1186/s12915-016-0270-5 Text en © Chomiak et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Chomiak, Taylor
Hung, Johanna
Nguyen, Minh Dang
Hu, Bin
Somato-dendritic decoupling as a novel mechanism for protracted cortical maturation
title Somato-dendritic decoupling as a novel mechanism for protracted cortical maturation
title_full Somato-dendritic decoupling as a novel mechanism for protracted cortical maturation
title_fullStr Somato-dendritic decoupling as a novel mechanism for protracted cortical maturation
title_full_unstemmed Somato-dendritic decoupling as a novel mechanism for protracted cortical maturation
title_short Somato-dendritic decoupling as a novel mechanism for protracted cortical maturation
title_sort somato-dendritic decoupling as a novel mechanism for protracted cortical maturation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4916537/
https://www.ncbi.nlm.nih.gov/pubmed/27328836
http://dx.doi.org/10.1186/s12915-016-0270-5
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