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A receptor-based analysis of local ecosystems in the human brain

BACKGROUND: As a complex system, the brain is a self-organizing entity that depends on local interactions among cells. Its regions (anatomically defined nuclei and areas) can be conceptualized as cellular ecosystems, but the similarity of their functional profiles is poorly understood. The study use...

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Autor principal: Janušonis, Skirmantas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5360078/
https://www.ncbi.nlm.nih.gov/pubmed/28320311
http://dx.doi.org/10.1186/s12868-017-0355-2
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author Janušonis, Skirmantas
author_facet Janušonis, Skirmantas
author_sort Janušonis, Skirmantas
collection PubMed
description BACKGROUND: As a complex system, the brain is a self-organizing entity that depends on local interactions among cells. Its regions (anatomically defined nuclei and areas) can be conceptualized as cellular ecosystems, but the similarity of their functional profiles is poorly understood. The study used the Allen Human Brain Atlas to classify 169 brain regions into hierarchically-organized environments based on their expression of 100 G protein-coupled neurotransmitter receptors, with no a priori reference to the regions’ positions in the brain’s anatomy or function. The analysis was based on hierarchical clustering, and multiscale bootstrap resampling was used to estimate the reliability of detected clusters. RESULTS: The study presents the first unbiased, hierarchical tree of functional environments in the human brain. The similarity of brain regions was strongly influenced by their anatomical proximity, even when they belonged to different functional systems. Generally, spatial vicinity trumped long-range projections or network connectivity. The main cluster of brain regions excluded the dentate gyrus of the hippocampus. The nuclei of the amygdala formed a cluster irrespective of their striatal or pallial origin. In its receptor profile, the hypothalamus was more closely associated with the midbrain than with the thalamus. The cerebellar cortical areas formed a tight and exclusive cluster. Most of the neocortical areas (with the exception of some occipital areas) clustered in a large, statistically well supported group that included no other brain regions. CONCLUSIONS: This study adds a new dimension to the established classifications of brain divisions. In a single framework, they are reconsidered at multiple scales—from individual nuclei and areas to their groups to the entire brain. The analysis provides support for predictive models of brain self-organization and adaptation.
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spelling pubmed-53600782017-03-24 A receptor-based analysis of local ecosystems in the human brain Janušonis, Skirmantas BMC Neurosci Research Article BACKGROUND: As a complex system, the brain is a self-organizing entity that depends on local interactions among cells. Its regions (anatomically defined nuclei and areas) can be conceptualized as cellular ecosystems, but the similarity of their functional profiles is poorly understood. The study used the Allen Human Brain Atlas to classify 169 brain regions into hierarchically-organized environments based on their expression of 100 G protein-coupled neurotransmitter receptors, with no a priori reference to the regions’ positions in the brain’s anatomy or function. The analysis was based on hierarchical clustering, and multiscale bootstrap resampling was used to estimate the reliability of detected clusters. RESULTS: The study presents the first unbiased, hierarchical tree of functional environments in the human brain. The similarity of brain regions was strongly influenced by their anatomical proximity, even when they belonged to different functional systems. Generally, spatial vicinity trumped long-range projections or network connectivity. The main cluster of brain regions excluded the dentate gyrus of the hippocampus. The nuclei of the amygdala formed a cluster irrespective of their striatal or pallial origin. In its receptor profile, the hypothalamus was more closely associated with the midbrain than with the thalamus. The cerebellar cortical areas formed a tight and exclusive cluster. Most of the neocortical areas (with the exception of some occipital areas) clustered in a large, statistically well supported group that included no other brain regions. CONCLUSIONS: This study adds a new dimension to the established classifications of brain divisions. In a single framework, they are reconsidered at multiple scales—from individual nuclei and areas to their groups to the entire brain. The analysis provides support for predictive models of brain self-organization and adaptation. BioMed Central 2017-03-20 /pmc/articles/PMC5360078/ /pubmed/28320311 http://dx.doi.org/10.1186/s12868-017-0355-2 Text en © The Author(s) 2017 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
Janušonis, Skirmantas
A receptor-based analysis of local ecosystems in the human brain
title A receptor-based analysis of local ecosystems in the human brain
title_full A receptor-based analysis of local ecosystems in the human brain
title_fullStr A receptor-based analysis of local ecosystems in the human brain
title_full_unstemmed A receptor-based analysis of local ecosystems in the human brain
title_short A receptor-based analysis of local ecosystems in the human brain
title_sort receptor-based analysis of local ecosystems in the human brain
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5360078/
https://www.ncbi.nlm.nih.gov/pubmed/28320311
http://dx.doi.org/10.1186/s12868-017-0355-2
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