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Microglia subtypes in acute, subacute, and chronic multiple sclerosis
The study was designed to examine microglia morphology in early and late forms of multiple sclerosis (MS). Archival paraffin embedded tissue samples from 25 cases were examined immunohistochemically. Pío del Río Hortega reported that phagocytes in acute focal destructive CNS lesions develop from mic...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10357941/ https://www.ncbi.nlm.nih.gov/pubmed/37344153 http://dx.doi.org/10.1093/jnen/nlad046 |
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author | Prineas, John W Lee, Sandra |
author_facet | Prineas, John W Lee, Sandra |
author_sort | Prineas, John W |
collection | PubMed |
description | The study was designed to examine microglia morphology in early and late forms of multiple sclerosis (MS). Archival paraffin embedded tissue samples from 25 cases were examined immunohistochemically. Pío del Río Hortega reported that phagocytes in acute focal destructive CNS lesions develop from microglia with no early contribution from infiltrating monocytes. In this study, we were unable to identify the changes cited by del Río Hortega in support of his theory. Instead, myelin phagocytes in MS appear to originate chiefly from infiltrating monocytes. In 4 cases, walls composed of MHC class II antigen-positive “wall microglia” were observed at plaque margins separating demyelinated and bordering myelinated tissue. Wall microglia in 2 plaques were accompanied by AQP4-positive fiber-forming astrocytes. In chronic but not early disease MS cases, microglia were seen to interact with infiltrating monocytes to form microglial nodules of several types. Also, MHC II-positive “activated” microglia in bordering intact tissue were exceptionally prominent where there was little evidence of ongoing myelin loss. It is concluded that myelin phagocytes in MS derive entirely from infiltrating MRP14-positive monocytes and not from resident microglia and that Río Hortega’s microglia play an anti-inflammatory role in MS and not the destructive role favored by the current literature. |
format | Online Article Text |
id | pubmed-10357941 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-103579412023-07-21 Microglia subtypes in acute, subacute, and chronic multiple sclerosis Prineas, John W Lee, Sandra J Neuropathol Exp Neurol Original Article The study was designed to examine microglia morphology in early and late forms of multiple sclerosis (MS). Archival paraffin embedded tissue samples from 25 cases were examined immunohistochemically. Pío del Río Hortega reported that phagocytes in acute focal destructive CNS lesions develop from microglia with no early contribution from infiltrating monocytes. In this study, we were unable to identify the changes cited by del Río Hortega in support of his theory. Instead, myelin phagocytes in MS appear to originate chiefly from infiltrating monocytes. In 4 cases, walls composed of MHC class II antigen-positive “wall microglia” were observed at plaque margins separating demyelinated and bordering myelinated tissue. Wall microglia in 2 plaques were accompanied by AQP4-positive fiber-forming astrocytes. In chronic but not early disease MS cases, microglia were seen to interact with infiltrating monocytes to form microglial nodules of several types. Also, MHC II-positive “activated” microglia in bordering intact tissue were exceptionally prominent where there was little evidence of ongoing myelin loss. It is concluded that myelin phagocytes in MS derive entirely from infiltrating MRP14-positive monocytes and not from resident microglia and that Río Hortega’s microglia play an anti-inflammatory role in MS and not the destructive role favored by the current literature. Oxford University Press 2023-06-21 /pmc/articles/PMC10357941/ /pubmed/37344153 http://dx.doi.org/10.1093/jnen/nlad046 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of American Association of Neuropathologists, Inc. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Original Article Prineas, John W Lee, Sandra Microglia subtypes in acute, subacute, and chronic multiple sclerosis |
title | Microglia subtypes in acute, subacute, and chronic multiple sclerosis |
title_full | Microglia subtypes in acute, subacute, and chronic multiple sclerosis |
title_fullStr | Microglia subtypes in acute, subacute, and chronic multiple sclerosis |
title_full_unstemmed | Microglia subtypes in acute, subacute, and chronic multiple sclerosis |
title_short | Microglia subtypes in acute, subacute, and chronic multiple sclerosis |
title_sort | microglia subtypes in acute, subacute, and chronic multiple sclerosis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10357941/ https://www.ncbi.nlm.nih.gov/pubmed/37344153 http://dx.doi.org/10.1093/jnen/nlad046 |
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