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Microglia as hackers of the matrix: sculpting synapses and the extracellular space
Microglia shape the synaptic environment in health and disease, but synapses do not exist in a vacuum. Instead, pre- and postsynaptic terminals are surrounded by extracellular matrix (ECM), which together with glia comprise the four elements of the contemporary tetrapartite synapse model. While rese...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8546068/ https://www.ncbi.nlm.nih.gov/pubmed/34413489 http://dx.doi.org/10.1038/s41423-021-00751-3 |
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author | Crapser, Joshua D. Arreola, Miguel A. Tsourmas, Kate I. Green, Kim N. |
author_facet | Crapser, Joshua D. Arreola, Miguel A. Tsourmas, Kate I. Green, Kim N. |
author_sort | Crapser, Joshua D. |
collection | PubMed |
description | Microglia shape the synaptic environment in health and disease, but synapses do not exist in a vacuum. Instead, pre- and postsynaptic terminals are surrounded by extracellular matrix (ECM), which together with glia comprise the four elements of the contemporary tetrapartite synapse model. While research in this area is still just beginning, accumulating evidence points toward a novel role for microglia in regulating the ECM during normal brain homeostasis, and such processes may, in turn, become dysfunctional in disease. As it relates to synapses, microglia are reported to modify the perisynaptic matrix, which is the diffuse matrix that surrounds dendritic and axonal terminals, as well as perineuronal nets (PNNs), specialized reticular formations of compact ECM that enwrap neuronal subsets and stabilize proximal synapses. The interconnected relationship between synapses and the ECM in which they are embedded suggests that alterations in one structure necessarily affect the dynamics of the other, and microglia may need to sculpt the matrix to modify the synapses within. Here, we provide an overview of the microglial regulation of synapses, perisynaptic matrix, and PNNs, propose candidate mechanisms by which these structures may be modified, and present the implications of such modifications in normal brain homeostasis and in disease. |
format | Online Article Text |
id | pubmed-8546068 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-85460682021-10-29 Microglia as hackers of the matrix: sculpting synapses and the extracellular space Crapser, Joshua D. Arreola, Miguel A. Tsourmas, Kate I. Green, Kim N. Cell Mol Immunol Review Article Microglia shape the synaptic environment in health and disease, but synapses do not exist in a vacuum. Instead, pre- and postsynaptic terminals are surrounded by extracellular matrix (ECM), which together with glia comprise the four elements of the contemporary tetrapartite synapse model. While research in this area is still just beginning, accumulating evidence points toward a novel role for microglia in regulating the ECM during normal brain homeostasis, and such processes may, in turn, become dysfunctional in disease. As it relates to synapses, microglia are reported to modify the perisynaptic matrix, which is the diffuse matrix that surrounds dendritic and axonal terminals, as well as perineuronal nets (PNNs), specialized reticular formations of compact ECM that enwrap neuronal subsets and stabilize proximal synapses. The interconnected relationship between synapses and the ECM in which they are embedded suggests that alterations in one structure necessarily affect the dynamics of the other, and microglia may need to sculpt the matrix to modify the synapses within. Here, we provide an overview of the microglial regulation of synapses, perisynaptic matrix, and PNNs, propose candidate mechanisms by which these structures may be modified, and present the implications of such modifications in normal brain homeostasis and in disease. Nature Publishing Group UK 2021-08-19 2021-11 /pmc/articles/PMC8546068/ /pubmed/34413489 http://dx.doi.org/10.1038/s41423-021-00751-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Article Crapser, Joshua D. Arreola, Miguel A. Tsourmas, Kate I. Green, Kim N. Microglia as hackers of the matrix: sculpting synapses and the extracellular space |
title | Microglia as hackers of the matrix: sculpting synapses and the extracellular space |
title_full | Microglia as hackers of the matrix: sculpting synapses and the extracellular space |
title_fullStr | Microglia as hackers of the matrix: sculpting synapses and the extracellular space |
title_full_unstemmed | Microglia as hackers of the matrix: sculpting synapses and the extracellular space |
title_short | Microglia as hackers of the matrix: sculpting synapses and the extracellular space |
title_sort | microglia as hackers of the matrix: sculpting synapses and the extracellular space |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8546068/ https://www.ncbi.nlm.nih.gov/pubmed/34413489 http://dx.doi.org/10.1038/s41423-021-00751-3 |
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