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Human prefrontal layer II interneurons in areas 46, 10 and 24
BACKGROUND: Prefrontal cortex (PFC) represents the highest level of integration and control of psychic and behavioral states. Several dysfunctions such as autism, hyperactivity disorders, depression, and schizophrenia have been related with alterations in the prefrontal cortex (PFC). Among the corti...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Universidad del Valle
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4437283/ https://www.ncbi.nlm.nih.gov/pubmed/26019381 |
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author | Arteaga, Gabriel Buritica, Efrain Escobar, Martha Isabel Pimienta, Hernan |
author_facet | Arteaga, Gabriel Buritica, Efrain Escobar, Martha Isabel Pimienta, Hernan |
author_sort | Arteaga, Gabriel |
collection | PubMed |
description | BACKGROUND: Prefrontal cortex (PFC) represents the highest level of integration and control of psychic and behavioral states. Several dysfunctions such as autism, hyperactivity disorders, depression, and schizophrenia have been related with alterations in the prefrontal cortex (PFC). Among the cortical layers of the PFC, layer II shows a particular vertical pattern of organization, the highest cell density and the biggest non-pyramidal/pyramidal neuronal ratio. We currently characterized the layer II cytoarchitecture in human areas 10, 24, and 46. OBJECTIVE: We focused particularly on the inhibitory neurons taking into account that these cells are involved in sustained firing (SF) after stimuli disappearance. METHODS: Postmortem samples from five subjects who died by causes different to central nervous system diseases were studied. Immunohistochemistry for the neuronal markers, NeuN, parvalbumin (PV), calbindin (CB), and calretinin (CR) were used. NeuN targeted the total neuronal population while the rest of the markers specifically the interneurons. RESULTS: Cell density and soma size were statically different between areas 10, 46, 24 when using NeuN. Layer II of area 46 showed the highest cell density. Regarding interneurons, PV+-cells of area 46 showed the highest density and size, in accordance to the proposal of a dual origin of the cerebral cortex. Interhemispheric asymmetries were not identified between homologue areas. CONCLUSION: First, our findings suggest that layer II of area 46 exhibits the most powerful inhibitory system compared to the other prefrontal areas analyzed. This feature is not only characteristic of the PFC but also supports a particular role of layer II of area 46 in SF. Additionally, known functional asymmetries between hemispheres might not be supported by morphological asymmetries. |
format | Online Article Text |
id | pubmed-4437283 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Universidad del Valle |
record_format | MEDLINE/PubMed |
spelling | pubmed-44372832015-05-27 Human prefrontal layer II interneurons in areas 46, 10 and 24 Arteaga, Gabriel Buritica, Efrain Escobar, Martha Isabel Pimienta, Hernan Colomb Med (Cali) Original Article BACKGROUND: Prefrontal cortex (PFC) represents the highest level of integration and control of psychic and behavioral states. Several dysfunctions such as autism, hyperactivity disorders, depression, and schizophrenia have been related with alterations in the prefrontal cortex (PFC). Among the cortical layers of the PFC, layer II shows a particular vertical pattern of organization, the highest cell density and the biggest non-pyramidal/pyramidal neuronal ratio. We currently characterized the layer II cytoarchitecture in human areas 10, 24, and 46. OBJECTIVE: We focused particularly on the inhibitory neurons taking into account that these cells are involved in sustained firing (SF) after stimuli disappearance. METHODS: Postmortem samples from five subjects who died by causes different to central nervous system diseases were studied. Immunohistochemistry for the neuronal markers, NeuN, parvalbumin (PV), calbindin (CB), and calretinin (CR) were used. NeuN targeted the total neuronal population while the rest of the markers specifically the interneurons. RESULTS: Cell density and soma size were statically different between areas 10, 46, 24 when using NeuN. Layer II of area 46 showed the highest cell density. Regarding interneurons, PV+-cells of area 46 showed the highest density and size, in accordance to the proposal of a dual origin of the cerebral cortex. Interhemispheric asymmetries were not identified between homologue areas. CONCLUSION: First, our findings suggest that layer II of area 46 exhibits the most powerful inhibitory system compared to the other prefrontal areas analyzed. This feature is not only characteristic of the PFC but also supports a particular role of layer II of area 46 in SF. Additionally, known functional asymmetries between hemispheres might not be supported by morphological asymmetries. Universidad del Valle 2015-03-30 /pmc/articles/PMC4437283/ /pubmed/26019381 Text en http://creativecommons.org/licenses/by/3.0/ © 2015 Universidad del Valle. This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited |
spellingShingle | Original Article Arteaga, Gabriel Buritica, Efrain Escobar, Martha Isabel Pimienta, Hernan Human prefrontal layer II interneurons in areas 46, 10 and 24 |
title | Human prefrontal layer II interneurons in areas 46, 10 and 24
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title_full | Human prefrontal layer II interneurons in areas 46, 10 and 24
|
title_fullStr | Human prefrontal layer II interneurons in areas 46, 10 and 24
|
title_full_unstemmed | Human prefrontal layer II interneurons in areas 46, 10 and 24
|
title_short | Human prefrontal layer II interneurons in areas 46, 10 and 24
|
title_sort | human prefrontal layer ii interneurons in areas 46, 10 and 24 |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4437283/ https://www.ncbi.nlm.nih.gov/pubmed/26019381 |
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