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Decreased Oligodendrocyte Number in Hippocampal Subfield CA4 in Schizophrenia: A Replication Study

Hippocampus-related cognitive deficits in working and verbal memory are frequent in schizophrenia, and hippocampal volume loss, particularly in the cornu ammonis (CA) subregions, was shown by magnetic resonance imaging studies. However, the underlying cellular alterations remain elusive. By using un...

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Autores principales: Schmitt, Andrea, Tatsch, Laura, Vollhardt, Alisa, Schneider-Axmann, Thomas, Raabe, Florian J., Roell, Lukas, Heinsen, Helmut, Hof, Patrick R., Falkai, Peter, Schmitz, Christoph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9600243/
https://www.ncbi.nlm.nih.gov/pubmed/36291109
http://dx.doi.org/10.3390/cells11203242
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author Schmitt, Andrea
Tatsch, Laura
Vollhardt, Alisa
Schneider-Axmann, Thomas
Raabe, Florian J.
Roell, Lukas
Heinsen, Helmut
Hof, Patrick R.
Falkai, Peter
Schmitz, Christoph
author_facet Schmitt, Andrea
Tatsch, Laura
Vollhardt, Alisa
Schneider-Axmann, Thomas
Raabe, Florian J.
Roell, Lukas
Heinsen, Helmut
Hof, Patrick R.
Falkai, Peter
Schmitz, Christoph
author_sort Schmitt, Andrea
collection PubMed
description Hippocampus-related cognitive deficits in working and verbal memory are frequent in schizophrenia, and hippocampal volume loss, particularly in the cornu ammonis (CA) subregions, was shown by magnetic resonance imaging studies. However, the underlying cellular alterations remain elusive. By using unbiased design-based stereology, we reported a reduction in oligodendrocyte number in CA4 in schizophrenia and of granular neurons in the dentate gyrus (DG). Here, we aimed to replicate these findings in an independent sample. We used a stereological approach to investigate the numbers and densities of neurons, oligodendrocytes, and astrocytes in CA4 and of granular neurons in the DG of left and right hemispheres in 11 brains from men with schizophrenia and 11 brains from age- and sex-matched healthy controls. In schizophrenia, a decreased number and density of oligodendrocytes was detected in the left and right CA4, whereas mean volumes of CA4 and the DG and the numbers and density of neurons, astrocytes, and granular neurons were not different in patients and controls, even after adjustment of variables because of positive correlations with postmortem interval and age. Our results replicate the previously described decrease in oligodendrocytes bilaterally in CA4 in schizophrenia and point to a deficit in oligodendrocyte maturation or a loss of mature oligodendrocytes. These changes result in impaired myelination and neuronal decoupling, both of which are linked to altered functional connectivity and subsequent cognitive dysfunction in schizophrenia.
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spelling pubmed-96002432022-10-27 Decreased Oligodendrocyte Number in Hippocampal Subfield CA4 in Schizophrenia: A Replication Study Schmitt, Andrea Tatsch, Laura Vollhardt, Alisa Schneider-Axmann, Thomas Raabe, Florian J. Roell, Lukas Heinsen, Helmut Hof, Patrick R. Falkai, Peter Schmitz, Christoph Cells Article Hippocampus-related cognitive deficits in working and verbal memory are frequent in schizophrenia, and hippocampal volume loss, particularly in the cornu ammonis (CA) subregions, was shown by magnetic resonance imaging studies. However, the underlying cellular alterations remain elusive. By using unbiased design-based stereology, we reported a reduction in oligodendrocyte number in CA4 in schizophrenia and of granular neurons in the dentate gyrus (DG). Here, we aimed to replicate these findings in an independent sample. We used a stereological approach to investigate the numbers and densities of neurons, oligodendrocytes, and astrocytes in CA4 and of granular neurons in the DG of left and right hemispheres in 11 brains from men with schizophrenia and 11 brains from age- and sex-matched healthy controls. In schizophrenia, a decreased number and density of oligodendrocytes was detected in the left and right CA4, whereas mean volumes of CA4 and the DG and the numbers and density of neurons, astrocytes, and granular neurons were not different in patients and controls, even after adjustment of variables because of positive correlations with postmortem interval and age. Our results replicate the previously described decrease in oligodendrocytes bilaterally in CA4 in schizophrenia and point to a deficit in oligodendrocyte maturation or a loss of mature oligodendrocytes. These changes result in impaired myelination and neuronal decoupling, both of which are linked to altered functional connectivity and subsequent cognitive dysfunction in schizophrenia. MDPI 2022-10-15 /pmc/articles/PMC9600243/ /pubmed/36291109 http://dx.doi.org/10.3390/cells11203242 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Schmitt, Andrea
Tatsch, Laura
Vollhardt, Alisa
Schneider-Axmann, Thomas
Raabe, Florian J.
Roell, Lukas
Heinsen, Helmut
Hof, Patrick R.
Falkai, Peter
Schmitz, Christoph
Decreased Oligodendrocyte Number in Hippocampal Subfield CA4 in Schizophrenia: A Replication Study
title Decreased Oligodendrocyte Number in Hippocampal Subfield CA4 in Schizophrenia: A Replication Study
title_full Decreased Oligodendrocyte Number in Hippocampal Subfield CA4 in Schizophrenia: A Replication Study
title_fullStr Decreased Oligodendrocyte Number in Hippocampal Subfield CA4 in Schizophrenia: A Replication Study
title_full_unstemmed Decreased Oligodendrocyte Number in Hippocampal Subfield CA4 in Schizophrenia: A Replication Study
title_short Decreased Oligodendrocyte Number in Hippocampal Subfield CA4 in Schizophrenia: A Replication Study
title_sort decreased oligodendrocyte number in hippocampal subfield ca4 in schizophrenia: a replication study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9600243/
https://www.ncbi.nlm.nih.gov/pubmed/36291109
http://dx.doi.org/10.3390/cells11203242
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