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Altered gene expression in the dorsolateral prefrontal cortex of individuals with schizophrenia

The underlying pathology of schizophrenia (SZ) is likely as heterogeneous as its symptomatology. A variety of cortical and subcortical regions, including the prefrontal cortex, have been implicated in its pathology, and a number of genes have been identified as risk factors for disease development....

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Autores principales: Guillozet-Bongaarts, A L, Hyde, T M, Dalley, R A, Hawrylycz, M J, Henry, A, Hof, P R, Hohmann, J, Jones, A R, Kuan, C L, Royall, J, Shen, E, Swanson, B, Zeng, H, Kleinman, J E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3965839/
https://www.ncbi.nlm.nih.gov/pubmed/23528911
http://dx.doi.org/10.1038/mp.2013.30
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author Guillozet-Bongaarts, A L
Hyde, T M
Dalley, R A
Hawrylycz, M J
Henry, A
Hof, P R
Hohmann, J
Jones, A R
Kuan, C L
Royall, J
Shen, E
Swanson, B
Zeng, H
Kleinman, J E
author_facet Guillozet-Bongaarts, A L
Hyde, T M
Dalley, R A
Hawrylycz, M J
Henry, A
Hof, P R
Hohmann, J
Jones, A R
Kuan, C L
Royall, J
Shen, E
Swanson, B
Zeng, H
Kleinman, J E
author_sort Guillozet-Bongaarts, A L
collection PubMed
description The underlying pathology of schizophrenia (SZ) is likely as heterogeneous as its symptomatology. A variety of cortical and subcortical regions, including the prefrontal cortex, have been implicated in its pathology, and a number of genes have been identified as risk factors for disease development. We used in situ hybridization (ISH) to examine the expression of 58 genes in the dorsolateral prefrontal cortex (DLPFC, comprised of Brodmann areas 9 and 46) from 19 individuals with a premorbid diagnosis of SZ and 33 control individuals. Genes were selected based on: (1) previous identification as risk factors for SZ; (2) cell type markers or (3) laminar markers. Cell density and staining intensity were compared in the DLPFC, as well as separately in Brodmann areas 9 and 46. The expression patterns of a variety of genes, many of which are associated with the GABAergic system, were altered in SZ when compared with controls. Additional genes, including C8orf79 and NR4A2, showed alterations in cell density or staining intensity between the groups, highlighting the need for additional studies. Alterations were, with only a few exceptions, limited to Brodmann area 9, suggesting regional specificity of pathology in the DLPFC. Our results agree with previous studies on the GABAergic involvement in SZ, and suggest that areas 9 and 46 may be differentially affected in the disease. This study also highlights additional genes that may be altered in SZ, and indicates that these potentially interesting genes can be identified by ISH and high-throughput image analysis techniques.
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spelling pubmed-39658392014-03-27 Altered gene expression in the dorsolateral prefrontal cortex of individuals with schizophrenia Guillozet-Bongaarts, A L Hyde, T M Dalley, R A Hawrylycz, M J Henry, A Hof, P R Hohmann, J Jones, A R Kuan, C L Royall, J Shen, E Swanson, B Zeng, H Kleinman, J E Mol Psychiatry Original Article The underlying pathology of schizophrenia (SZ) is likely as heterogeneous as its symptomatology. A variety of cortical and subcortical regions, including the prefrontal cortex, have been implicated in its pathology, and a number of genes have been identified as risk factors for disease development. We used in situ hybridization (ISH) to examine the expression of 58 genes in the dorsolateral prefrontal cortex (DLPFC, comprised of Brodmann areas 9 and 46) from 19 individuals with a premorbid diagnosis of SZ and 33 control individuals. Genes were selected based on: (1) previous identification as risk factors for SZ; (2) cell type markers or (3) laminar markers. Cell density and staining intensity were compared in the DLPFC, as well as separately in Brodmann areas 9 and 46. The expression patterns of a variety of genes, many of which are associated with the GABAergic system, were altered in SZ when compared with controls. Additional genes, including C8orf79 and NR4A2, showed alterations in cell density or staining intensity between the groups, highlighting the need for additional studies. Alterations were, with only a few exceptions, limited to Brodmann area 9, suggesting regional specificity of pathology in the DLPFC. Our results agree with previous studies on the GABAergic involvement in SZ, and suggest that areas 9 and 46 may be differentially affected in the disease. This study also highlights additional genes that may be altered in SZ, and indicates that these potentially interesting genes can be identified by ISH and high-throughput image analysis techniques. Nature Publishing Group 2014-04 2013-03-26 /pmc/articles/PMC3965839/ /pubmed/23528911 http://dx.doi.org/10.1038/mp.2013.30 Text en Copyright © 2014 Macmillan Publishers Limited http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Original Article
Guillozet-Bongaarts, A L
Hyde, T M
Dalley, R A
Hawrylycz, M J
Henry, A
Hof, P R
Hohmann, J
Jones, A R
Kuan, C L
Royall, J
Shen, E
Swanson, B
Zeng, H
Kleinman, J E
Altered gene expression in the dorsolateral prefrontal cortex of individuals with schizophrenia
title Altered gene expression in the dorsolateral prefrontal cortex of individuals with schizophrenia
title_full Altered gene expression in the dorsolateral prefrontal cortex of individuals with schizophrenia
title_fullStr Altered gene expression in the dorsolateral prefrontal cortex of individuals with schizophrenia
title_full_unstemmed Altered gene expression in the dorsolateral prefrontal cortex of individuals with schizophrenia
title_short Altered gene expression in the dorsolateral prefrontal cortex of individuals with schizophrenia
title_sort altered gene expression in the dorsolateral prefrontal cortex of individuals with schizophrenia
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3965839/
https://www.ncbi.nlm.nih.gov/pubmed/23528911
http://dx.doi.org/10.1038/mp.2013.30
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