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Fibrosis of the Choroid Plexus Filtration Membrane
We report a previously undescribed inflammatory lesion consisting of deposition of activated complement (C3d and C9neo) in association with major histocompatibility complex type II (MHC2)-positive activated microglia in choroid plexus villi exhibiting classical fibrous thickening of the pericapillar...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5015658/ https://www.ncbi.nlm.nih.gov/pubmed/27444353 http://dx.doi.org/10.1093/jnen/nlw061 |
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author | Prineas, John W. Parratt, John D. E. Kirwan, Paul D. |
author_facet | Prineas, John W. Parratt, John D. E. Kirwan, Paul D. |
author_sort | Prineas, John W. |
collection | PubMed |
description | We report a previously undescribed inflammatory lesion consisting of deposition of activated complement (C3d and C9neo) in association with major histocompatibility complex type II (MHC2)-positive activated microglia in choroid plexus villi exhibiting classical fibrous thickening of the pericapillary filtration membrane. The proportion of villi affected ranged from 5% to 90% in 56 adult subjects with diseases of the CNS and 11 subjects with no preexisting disease of the CNS. In 3 of the 4 children studied, 2% or less of examined villi showed stromal thickening, complement deposition, and the presence of MHC2-positive microglia; in adults, the proportion of villi affected increased with age. Other features of the lesion included loss of capillaries and failure by macrophages to clear extracellular particulate electron-dense material by clathrin-mediated phagocytosis. This choroid plexus lesion may relate pathogenetically to age-related macular degeneration and to Alzheimer disease, 2 other conditions with no known risk factors other than increasing age. All 3 conditions are characterized by the presence of damaged capillaries, inflammatory extracellular aggregates of mixed molecular composition and defective clearance of the deposits by macrophages. |
format | Online Article Text |
id | pubmed-5015658 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-50156582016-09-09 Fibrosis of the Choroid Plexus Filtration Membrane Prineas, John W. Parratt, John D. E. Kirwan, Paul D. J Neuropathol Exp Neurol Original Articles We report a previously undescribed inflammatory lesion consisting of deposition of activated complement (C3d and C9neo) in association with major histocompatibility complex type II (MHC2)-positive activated microglia in choroid plexus villi exhibiting classical fibrous thickening of the pericapillary filtration membrane. The proportion of villi affected ranged from 5% to 90% in 56 adult subjects with diseases of the CNS and 11 subjects with no preexisting disease of the CNS. In 3 of the 4 children studied, 2% or less of examined villi showed stromal thickening, complement deposition, and the presence of MHC2-positive microglia; in adults, the proportion of villi affected increased with age. Other features of the lesion included loss of capillaries and failure by macrophages to clear extracellular particulate electron-dense material by clathrin-mediated phagocytosis. This choroid plexus lesion may relate pathogenetically to age-related macular degeneration and to Alzheimer disease, 2 other conditions with no known risk factors other than increasing age. All 3 conditions are characterized by the presence of damaged capillaries, inflammatory extracellular aggregates of mixed molecular composition and defective clearance of the deposits by macrophages. Oxford University Press 2016-09 2016-07-19 /pmc/articles/PMC5015658/ /pubmed/27444353 http://dx.doi.org/10.1093/jnen/nlw061 Text en © 2016 Oxford University Press OR American Association of Neuropathologists. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://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 Articles Prineas, John W. Parratt, John D. E. Kirwan, Paul D. Fibrosis of the Choroid Plexus Filtration Membrane |
title | Fibrosis of the Choroid Plexus Filtration Membrane |
title_full | Fibrosis of the Choroid Plexus Filtration Membrane |
title_fullStr | Fibrosis of the Choroid Plexus Filtration Membrane |
title_full_unstemmed | Fibrosis of the Choroid Plexus Filtration Membrane |
title_short | Fibrosis of the Choroid Plexus Filtration Membrane |
title_sort | fibrosis of the choroid plexus filtration membrane |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5015658/ https://www.ncbi.nlm.nih.gov/pubmed/27444353 http://dx.doi.org/10.1093/jnen/nlw061 |
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