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Synapse-specific roles for microglia in development: New horizons in the prefrontal cortex
Dysfunction of both microglia and circuitry in the medial prefrontal cortex (mPFC) have been implicated in numerous neuropsychiatric disorders, but how microglia affect mPFC development in health and disease is not well understood. mPFC circuits undergo a prolonged maturation after birth that is dri...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9394540/ https://www.ncbi.nlm.nih.gov/pubmed/36003220 http://dx.doi.org/10.3389/fnmol.2022.965756 |
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author | Blagburn-Blanco, Sara V. Chappell, Megan S. De Biase, Lindsay M. DeNardo, Laura A. |
author_facet | Blagburn-Blanco, Sara V. Chappell, Megan S. De Biase, Lindsay M. DeNardo, Laura A. |
author_sort | Blagburn-Blanco, Sara V. |
collection | PubMed |
description | Dysfunction of both microglia and circuitry in the medial prefrontal cortex (mPFC) have been implicated in numerous neuropsychiatric disorders, but how microglia affect mPFC development in health and disease is not well understood. mPFC circuits undergo a prolonged maturation after birth that is driven by molecular programs and activity-dependent processes. Though this extended development is crucial to acquire mature cognitive abilities, it likely renders mPFC circuitry more susceptible to disruption by genetic and environmental insults that increase the risk of developing mental health disorders. Recent work suggests that microglia directly influence mPFC circuit maturation, though the biological factors underlying this observation remain unclear. In this review, we discuss these recent findings along with new studies on the cellular mechanisms by which microglia shape sensory circuits during postnatal development. We focus on the molecular pathways through which glial cells and immune signals regulate synaptogenesis and activity-dependent synaptic refinement. We further highlight how disruptions in these pathways are implicated in the pathogenesis of neurodevelopmental and psychiatric disorders associated with mPFC dysfunction, including schizophrenia and autism spectrum disorder (ASD). Using these disorders as a framework, we discuss microglial mechanisms that could link environmental risk factors including infections and stress with ongoing genetic programs to aberrantly shape mPFC circuitry. |
format | Online Article Text |
id | pubmed-9394540 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93945402022-08-23 Synapse-specific roles for microglia in development: New horizons in the prefrontal cortex Blagburn-Blanco, Sara V. Chappell, Megan S. De Biase, Lindsay M. DeNardo, Laura A. Front Mol Neurosci Molecular Neuroscience Dysfunction of both microglia and circuitry in the medial prefrontal cortex (mPFC) have been implicated in numerous neuropsychiatric disorders, but how microglia affect mPFC development in health and disease is not well understood. mPFC circuits undergo a prolonged maturation after birth that is driven by molecular programs and activity-dependent processes. Though this extended development is crucial to acquire mature cognitive abilities, it likely renders mPFC circuitry more susceptible to disruption by genetic and environmental insults that increase the risk of developing mental health disorders. Recent work suggests that microglia directly influence mPFC circuit maturation, though the biological factors underlying this observation remain unclear. In this review, we discuss these recent findings along with new studies on the cellular mechanisms by which microglia shape sensory circuits during postnatal development. We focus on the molecular pathways through which glial cells and immune signals regulate synaptogenesis and activity-dependent synaptic refinement. We further highlight how disruptions in these pathways are implicated in the pathogenesis of neurodevelopmental and psychiatric disorders associated with mPFC dysfunction, including schizophrenia and autism spectrum disorder (ASD). Using these disorders as a framework, we discuss microglial mechanisms that could link environmental risk factors including infections and stress with ongoing genetic programs to aberrantly shape mPFC circuitry. Frontiers Media S.A. 2022-08-08 /pmc/articles/PMC9394540/ /pubmed/36003220 http://dx.doi.org/10.3389/fnmol.2022.965756 Text en Copyright © 2022 Blagburn-Blanco, Chappell, De Biase and DeNardo. 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 | Molecular Neuroscience Blagburn-Blanco, Sara V. Chappell, Megan S. De Biase, Lindsay M. DeNardo, Laura A. Synapse-specific roles for microglia in development: New horizons in the prefrontal cortex |
title | Synapse-specific roles for microglia in development: New horizons in the prefrontal cortex |
title_full | Synapse-specific roles for microglia in development: New horizons in the prefrontal cortex |
title_fullStr | Synapse-specific roles for microglia in development: New horizons in the prefrontal cortex |
title_full_unstemmed | Synapse-specific roles for microglia in development: New horizons in the prefrontal cortex |
title_short | Synapse-specific roles for microglia in development: New horizons in the prefrontal cortex |
title_sort | synapse-specific roles for microglia in development: new horizons in the prefrontal cortex |
topic | Molecular Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9394540/ https://www.ncbi.nlm.nih.gov/pubmed/36003220 http://dx.doi.org/10.3389/fnmol.2022.965756 |
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