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Stereological Study of Amygdala Glial Populations in Adolescents and Adults with Autism Spectrum Disorder
The amygdala undergoes aberrant development in autism spectrum disorder (ASD). We previously found that there are reduced neuron numbers in the adult postmortem amygdala from individuals with ASD compared to typically developing controls. The current study is a comprehensive stereological examinatio...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4201518/ https://www.ncbi.nlm.nih.gov/pubmed/25330013 http://dx.doi.org/10.1371/journal.pone.0110356 |
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author | Morgan, John T. Barger, Nicole Amaral, David G. Schumann, Cynthia M. |
author_facet | Morgan, John T. Barger, Nicole Amaral, David G. Schumann, Cynthia M. |
author_sort | Morgan, John T. |
collection | PubMed |
description | The amygdala undergoes aberrant development in autism spectrum disorder (ASD). We previously found that there are reduced neuron numbers in the adult postmortem amygdala from individuals with ASD compared to typically developing controls. The current study is a comprehensive stereological examination of four non-neuronal cell populations: microglia, oligodendrocytes, astrocytes, and endothelial cells, in the same brains studied previously. We provide a detailed neuroanatomical protocol for defining each cell type that may be applied to other studies of the amygdala in neurodevelopmental and psychiatric disorders. We then assess whether cell numbers and average volumes differ between ASD and typically developing brains. We hypothesized that a reduction in neuron numbers in ASD might relate to altered immune function and/or aberrant microglial activation, as indicated by increased microglial number and cell body volume. Overall, average non-neuronal cell numbers and volumes did not differ between ASD and typically developing brains. However, there was evident heterogeneity within the ASD cohort. Two of the eight ASD brains displayed strong microglial activation. Contrary to our original hypothesis, there was a trend toward a positive correlation between neuronal and microglial numbers in both ASD and control cases. There were fewer oligodendrocytes in the amygdala of adult individuals with ASD ages 20 and older compared to typically developing controls. This finding may provide a possible sign of altered connectivity or impaired neuronal communication that may change across the lifespan in ASD. |
format | Online Article Text |
id | pubmed-4201518 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-42015182014-10-21 Stereological Study of Amygdala Glial Populations in Adolescents and Adults with Autism Spectrum Disorder Morgan, John T. Barger, Nicole Amaral, David G. Schumann, Cynthia M. PLoS One Research Article The amygdala undergoes aberrant development in autism spectrum disorder (ASD). We previously found that there are reduced neuron numbers in the adult postmortem amygdala from individuals with ASD compared to typically developing controls. The current study is a comprehensive stereological examination of four non-neuronal cell populations: microglia, oligodendrocytes, astrocytes, and endothelial cells, in the same brains studied previously. We provide a detailed neuroanatomical protocol for defining each cell type that may be applied to other studies of the amygdala in neurodevelopmental and psychiatric disorders. We then assess whether cell numbers and average volumes differ between ASD and typically developing brains. We hypothesized that a reduction in neuron numbers in ASD might relate to altered immune function and/or aberrant microglial activation, as indicated by increased microglial number and cell body volume. Overall, average non-neuronal cell numbers and volumes did not differ between ASD and typically developing brains. However, there was evident heterogeneity within the ASD cohort. Two of the eight ASD brains displayed strong microglial activation. Contrary to our original hypothesis, there was a trend toward a positive correlation between neuronal and microglial numbers in both ASD and control cases. There were fewer oligodendrocytes in the amygdala of adult individuals with ASD ages 20 and older compared to typically developing controls. This finding may provide a possible sign of altered connectivity or impaired neuronal communication that may change across the lifespan in ASD. Public Library of Science 2014-10-17 /pmc/articles/PMC4201518/ /pubmed/25330013 http://dx.doi.org/10.1371/journal.pone.0110356 Text en © 2014 Morgan et al http://creativecommons.org/licenses/by/4.0/ 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 properly credited. |
spellingShingle | Research Article Morgan, John T. Barger, Nicole Amaral, David G. Schumann, Cynthia M. Stereological Study of Amygdala Glial Populations in Adolescents and Adults with Autism Spectrum Disorder |
title | Stereological Study of Amygdala Glial Populations in Adolescents and Adults with Autism Spectrum Disorder |
title_full | Stereological Study of Amygdala Glial Populations in Adolescents and Adults with Autism Spectrum Disorder |
title_fullStr | Stereological Study of Amygdala Glial Populations in Adolescents and Adults with Autism Spectrum Disorder |
title_full_unstemmed | Stereological Study of Amygdala Glial Populations in Adolescents and Adults with Autism Spectrum Disorder |
title_short | Stereological Study of Amygdala Glial Populations in Adolescents and Adults with Autism Spectrum Disorder |
title_sort | stereological study of amygdala glial populations in adolescents and adults with autism spectrum disorder |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4201518/ https://www.ncbi.nlm.nih.gov/pubmed/25330013 http://dx.doi.org/10.1371/journal.pone.0110356 |
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