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Long-lasting perivascular accumulation of major histocompatibility complex class II-positive lipophages in the spinal cord of stroke patients: possible relevance for the immune privilege of the brain

Six cases of middle cerebral artery occlusion are presented in which the cellular changes accompanying descending degeneration of the lateral corticospinal tract were studied at different time points (5 days–10 years) following the insult. Microglia and perivascular cells were found to ingest large...

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Autores principales: Kösel, Siegfried, Egensperger, Rupert, Bise, Karl, Arbogast, Susanne, Mehraein, Parviz, Graeber, Manuel B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 1997
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7086531/
https://www.ncbi.nlm.nih.gov/pubmed/9444354
http://dx.doi.org/10.1007/s004010050747
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author Kösel, Siegfried
Egensperger, Rupert
Bise, Karl
Arbogast, Susanne
Mehraein, Parviz
Graeber, Manuel B.
author_facet Kösel, Siegfried
Egensperger, Rupert
Bise, Karl
Arbogast, Susanne
Mehraein, Parviz
Graeber, Manuel B.
author_sort Kösel, Siegfried
collection PubMed
description Six cases of middle cerebral artery occlusion are presented in which the cellular changes accompanying descending degeneration of the lateral corticospinal tract were studied at different time points (5 days–10 years) following the insult. Microglia and perivascular cells were found to ingest large amounts of myelin degradation products, while expressing high levels of major histocompatibility complex (MHC) class II molecules. Activation of perivascular macrophages, as indicated by increased class II expression, lasted for many years and appeared to follow down-regulation of both phagocytic activity and class II expression on parenchymal microglia. TUNEL labeling was absent from both microglia and perivascular cells at all time points investigated. Indirect evidence is presented that microglia may transfer myelin degradation products to the perivascular space. Perivascular cells which express MHC class II molecules constitutively do not appear to leave the perivascular compartment in large numbers and could release myelin degradation products into the cerebrospinal fluid. The possible immunological consequences of these findings are discussed with respect to their possible relevance for antigen presentation and autoimmune central nervous system disease.
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spelling pubmed-70865312020-03-23 Long-lasting perivascular accumulation of major histocompatibility complex class II-positive lipophages in the spinal cord of stroke patients: possible relevance for the immune privilege of the brain Kösel, Siegfried Egensperger, Rupert Bise, Karl Arbogast, Susanne Mehraein, Parviz Graeber, Manuel B. Acta Neuropathol Regular Paper Six cases of middle cerebral artery occlusion are presented in which the cellular changes accompanying descending degeneration of the lateral corticospinal tract were studied at different time points (5 days–10 years) following the insult. Microglia and perivascular cells were found to ingest large amounts of myelin degradation products, while expressing high levels of major histocompatibility complex (MHC) class II molecules. Activation of perivascular macrophages, as indicated by increased class II expression, lasted for many years and appeared to follow down-regulation of both phagocytic activity and class II expression on parenchymal microglia. TUNEL labeling was absent from both microglia and perivascular cells at all time points investigated. Indirect evidence is presented that microglia may transfer myelin degradation products to the perivascular space. Perivascular cells which express MHC class II molecules constitutively do not appear to leave the perivascular compartment in large numbers and could release myelin degradation products into the cerebrospinal fluid. The possible immunological consequences of these findings are discussed with respect to their possible relevance for antigen presentation and autoimmune central nervous system disease. Springer-Verlag 1997 /pmc/articles/PMC7086531/ /pubmed/9444354 http://dx.doi.org/10.1007/s004010050747 Text en © Springer-Verlag Berlin Heidelberg 1997 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Regular Paper
Kösel, Siegfried
Egensperger, Rupert
Bise, Karl
Arbogast, Susanne
Mehraein, Parviz
Graeber, Manuel B.
Long-lasting perivascular accumulation of major histocompatibility complex class II-positive lipophages in the spinal cord of stroke patients: possible relevance for the immune privilege of the brain
title Long-lasting perivascular accumulation of major histocompatibility complex class II-positive lipophages in the spinal cord of stroke patients: possible relevance for the immune privilege of the brain
title_full Long-lasting perivascular accumulation of major histocompatibility complex class II-positive lipophages in the spinal cord of stroke patients: possible relevance for the immune privilege of the brain
title_fullStr Long-lasting perivascular accumulation of major histocompatibility complex class II-positive lipophages in the spinal cord of stroke patients: possible relevance for the immune privilege of the brain
title_full_unstemmed Long-lasting perivascular accumulation of major histocompatibility complex class II-positive lipophages in the spinal cord of stroke patients: possible relevance for the immune privilege of the brain
title_short Long-lasting perivascular accumulation of major histocompatibility complex class II-positive lipophages in the spinal cord of stroke patients: possible relevance for the immune privilege of the brain
title_sort long-lasting perivascular accumulation of major histocompatibility complex class ii-positive lipophages in the spinal cord of stroke patients: possible relevance for the immune privilege of the brain
topic Regular Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7086531/
https://www.ncbi.nlm.nih.gov/pubmed/9444354
http://dx.doi.org/10.1007/s004010050747
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