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Direct association with the vascular basement membrane is a frequent feature of myelinating oligodendrocytes in the neocortex
BACKGROUND: Oligodendrocyte lineage cells interact with the vasculature in the gray matter. Physical and functional interactions between blood vessels and oligodendrocyte precursor cells play an essential role in both the developing and adult brain. Oligodendrocyte precursor cells have been shown to...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10069068/ https://www.ncbi.nlm.nih.gov/pubmed/37013659 http://dx.doi.org/10.1186/s12987-023-00425-4 |
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author | Palhol, Justine S. C. Balia, Maddalena Sánchez-Román Terán, Fernando Labarchède, Mélody Gontier, Etienne Battefeld, Arne |
author_facet | Palhol, Justine S. C. Balia, Maddalena Sánchez-Román Terán, Fernando Labarchède, Mélody Gontier, Etienne Battefeld, Arne |
author_sort | Palhol, Justine S. C. |
collection | PubMed |
description | BACKGROUND: Oligodendrocyte lineage cells interact with the vasculature in the gray matter. Physical and functional interactions between blood vessels and oligodendrocyte precursor cells play an essential role in both the developing and adult brain. Oligodendrocyte precursor cells have been shown to migrate along the vasculature and subsequently detach from it during their differentiation to oligodendrocytes. However, the association of mature oligodendrocytes with blood vessels has been noted since the discovery of this glial cell type almost a century ago, but this interaction remains poorly explored. RESULTS: Here, we systematically investigated the extent of mature oligodendrocyte interaction with the vasculature in mouse brain. We found that ~ 17% of oligodendrocytes were in contact with blood vessels in the neocortex, the hippocampal CA1 region and the cerebellar cortex. Contacts were made mainly with capillaries and sparsely with larger arterioles or venules. By combining light and serial electron microscopy, we demonstrated that oligodendrocytes are in direct contact with the vascular basement membrane, raising the possibility of direct signaling pathways and metabolite exchange with endothelial cells. During experimental remyelination in the adult, oligodendrocytes were regenerated and associated with blood vessels in the same proportion compared to control cortex, suggesting a homeostatic regulation of the vasculature-associated oligodendrocyte population. CONCLUSIONS: Based on their frequent and close association with blood vessels, we propose that vasculature-associated oligodendrocytes should be considered as an integral part of the brain vasculature microenvironment. This particular location could underlie specific functions of vasculature-associated oligodendrocytes, while contributing to the vulnerability of mature oligodendrocytes in neurological diseases. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12987-023-00425-4. |
format | Online Article Text |
id | pubmed-10069068 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-100690682023-04-04 Direct association with the vascular basement membrane is a frequent feature of myelinating oligodendrocytes in the neocortex Palhol, Justine S. C. Balia, Maddalena Sánchez-Román Terán, Fernando Labarchède, Mélody Gontier, Etienne Battefeld, Arne Fluids Barriers CNS Research BACKGROUND: Oligodendrocyte lineage cells interact with the vasculature in the gray matter. Physical and functional interactions between blood vessels and oligodendrocyte precursor cells play an essential role in both the developing and adult brain. Oligodendrocyte precursor cells have been shown to migrate along the vasculature and subsequently detach from it during their differentiation to oligodendrocytes. However, the association of mature oligodendrocytes with blood vessels has been noted since the discovery of this glial cell type almost a century ago, but this interaction remains poorly explored. RESULTS: Here, we systematically investigated the extent of mature oligodendrocyte interaction with the vasculature in mouse brain. We found that ~ 17% of oligodendrocytes were in contact with blood vessels in the neocortex, the hippocampal CA1 region and the cerebellar cortex. Contacts were made mainly with capillaries and sparsely with larger arterioles or venules. By combining light and serial electron microscopy, we demonstrated that oligodendrocytes are in direct contact with the vascular basement membrane, raising the possibility of direct signaling pathways and metabolite exchange with endothelial cells. During experimental remyelination in the adult, oligodendrocytes were regenerated and associated with blood vessels in the same proportion compared to control cortex, suggesting a homeostatic regulation of the vasculature-associated oligodendrocyte population. CONCLUSIONS: Based on their frequent and close association with blood vessels, we propose that vasculature-associated oligodendrocytes should be considered as an integral part of the brain vasculature microenvironment. This particular location could underlie specific functions of vasculature-associated oligodendrocytes, while contributing to the vulnerability of mature oligodendrocytes in neurological diseases. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12987-023-00425-4. BioMed Central 2023-04-03 /pmc/articles/PMC10069068/ /pubmed/37013659 http://dx.doi.org/10.1186/s12987-023-00425-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Palhol, Justine S. C. Balia, Maddalena Sánchez-Román Terán, Fernando Labarchède, Mélody Gontier, Etienne Battefeld, Arne Direct association with the vascular basement membrane is a frequent feature of myelinating oligodendrocytes in the neocortex |
title | Direct association with the vascular basement membrane is a frequent feature of myelinating oligodendrocytes in the neocortex |
title_full | Direct association with the vascular basement membrane is a frequent feature of myelinating oligodendrocytes in the neocortex |
title_fullStr | Direct association with the vascular basement membrane is a frequent feature of myelinating oligodendrocytes in the neocortex |
title_full_unstemmed | Direct association with the vascular basement membrane is a frequent feature of myelinating oligodendrocytes in the neocortex |
title_short | Direct association with the vascular basement membrane is a frequent feature of myelinating oligodendrocytes in the neocortex |
title_sort | direct association with the vascular basement membrane is a frequent feature of myelinating oligodendrocytes in the neocortex |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10069068/ https://www.ncbi.nlm.nih.gov/pubmed/37013659 http://dx.doi.org/10.1186/s12987-023-00425-4 |
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