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The Sexual Dimorphic Synapse: From Spine Density to Molecular Composition

A synaptic sexual dimorphism is relevant in the context of multiple neurodevelopmental, neurodegenerative, and neuropsychiatric disorders. Many of these disorders show a different prevalence and progression in woman and man. A similar variance is also present in corresponding animal models. To under...

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Detalles Bibliográficos
Autores principales: Uhl, Mara, Schmeisser, Michael J., Schumann, Sven
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8894598/
https://www.ncbi.nlm.nih.gov/pubmed/35250477
http://dx.doi.org/10.3389/fnmol.2022.818390
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author Uhl, Mara
Schmeisser, Michael J.
Schumann, Sven
author_facet Uhl, Mara
Schmeisser, Michael J.
Schumann, Sven
author_sort Uhl, Mara
collection PubMed
description A synaptic sexual dimorphism is relevant in the context of multiple neurodevelopmental, neurodegenerative, and neuropsychiatric disorders. Many of these disorders show a different prevalence and progression in woman and man. A similar variance is also present in corresponding animal models. To understand and characterize this dimorphism in pathologies it is important to first understand sex differences in unaffected individuals. Therefore, sexual differences have been studied since 1788, first focusing on brain weight, size, and volume. But as these measures are not directly related to brain function, the investigation of sexual dimorphism also expanded to other organizational levels of the brain. This review is focused on sexual dimorphism at the synaptic level, as these specialized structures are the smallest functional units of the brain, determining cell communication, connectivity, and plasticity. Multiple differences between males and females can be found on the levels of spine density, synaptic morphology, and molecular synapse composition. These differences support the importance of sex-disaggregated data. The specificity of changes to a particular brain region or circuit might support the idea of a mosaic brain, in which each tile individually lies on a continuum from masculinization to feminization. Moreover, synapses can be seen as the smallest tiles of the mosaic determining the classification of larger areas.
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spelling pubmed-88945982022-03-05 The Sexual Dimorphic Synapse: From Spine Density to Molecular Composition Uhl, Mara Schmeisser, Michael J. Schumann, Sven Front Mol Neurosci Neuroscience A synaptic sexual dimorphism is relevant in the context of multiple neurodevelopmental, neurodegenerative, and neuropsychiatric disorders. Many of these disorders show a different prevalence and progression in woman and man. A similar variance is also present in corresponding animal models. To understand and characterize this dimorphism in pathologies it is important to first understand sex differences in unaffected individuals. Therefore, sexual differences have been studied since 1788, first focusing on brain weight, size, and volume. But as these measures are not directly related to brain function, the investigation of sexual dimorphism also expanded to other organizational levels of the brain. This review is focused on sexual dimorphism at the synaptic level, as these specialized structures are the smallest functional units of the brain, determining cell communication, connectivity, and plasticity. Multiple differences between males and females can be found on the levels of spine density, synaptic morphology, and molecular synapse composition. These differences support the importance of sex-disaggregated data. The specificity of changes to a particular brain region or circuit might support the idea of a mosaic brain, in which each tile individually lies on a continuum from masculinization to feminization. Moreover, synapses can be seen as the smallest tiles of the mosaic determining the classification of larger areas. Frontiers Media S.A. 2022-02-18 /pmc/articles/PMC8894598/ /pubmed/35250477 http://dx.doi.org/10.3389/fnmol.2022.818390 Text en Copyright © 2022 Uhl, Schmeisser and Schumann. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Uhl, Mara
Schmeisser, Michael J.
Schumann, Sven
The Sexual Dimorphic Synapse: From Spine Density to Molecular Composition
title The Sexual Dimorphic Synapse: From Spine Density to Molecular Composition
title_full The Sexual Dimorphic Synapse: From Spine Density to Molecular Composition
title_fullStr The Sexual Dimorphic Synapse: From Spine Density to Molecular Composition
title_full_unstemmed The Sexual Dimorphic Synapse: From Spine Density to Molecular Composition
title_short The Sexual Dimorphic Synapse: From Spine Density to Molecular Composition
title_sort sexual dimorphic synapse: from spine density to molecular composition
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8894598/
https://www.ncbi.nlm.nih.gov/pubmed/35250477
http://dx.doi.org/10.3389/fnmol.2022.818390
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