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Oligodendroglial pathology in canine distemper

Canine distemper virus (CDV) causes a multifocal demyelinating disease in dogs. The mechanism of acute demyelination in distemper is still poorly understood. The initial demyelinating lesion in distemper is directly virus induced, since there is a clear correlation between the occurrence of demyelin...

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Autores principales: Zurbriggen, A., Schmid, I., Graber, H. U., Vandevelde, M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 1997
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7086659/
https://www.ncbi.nlm.nih.gov/pubmed/9452824
http://dx.doi.org/10.1007/s004010050767
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author Zurbriggen, A.
Schmid, I.
Graber, H. U.
Vandevelde, M.
author_facet Zurbriggen, A.
Schmid, I.
Graber, H. U.
Vandevelde, M.
author_sort Zurbriggen, A.
collection PubMed
description Canine distemper virus (CDV) causes a multifocal demyelinating disease in dogs. The mechanism of acute demyelination in distemper is still poorly understood. The initial demyelinating lesion in distemper is directly virus induced, since there is a clear correlation between the occurrence of demyelination and CDV replication in the cells of the white matter. Yet, there is little evidence for oligodendroglial infection. Changes of these cells have been reported in vitro and in vivo. The in vitro studies showed that – in contrast to other cells such as astrocytes and macrophages – oligodendrocytes hardly express CDV protein. However, we could show that these cells underwent a restricted infection with transcription of CDV RNA and that this phenomenon correlated with down-regulation of myelin gene transcription. The extension of these in vitro findings in vivo was obscured by the lack of reliable oligodendrocyte labelling techniques in canine brain tissue sections. In this study we combined immunohistochemistry with in situ hybridization to examine oligodendrocytes in demyelinating lesions and to investigate the question of oligodendrocyte infection in vivo. We could demonstrate that CDV infection leads to massive down-regulation of myelin gene expression in demyelinating lesions and that this effect correlates in part with a restricted infection of oligodendrocytes.
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spelling pubmed-70866592020-03-23 Oligodendroglial pathology in canine distemper Zurbriggen, A. Schmid, I. Graber, H. U. Vandevelde, M. Acta Neuropathol Regular Paper Canine distemper virus (CDV) causes a multifocal demyelinating disease in dogs. The mechanism of acute demyelination in distemper is still poorly understood. The initial demyelinating lesion in distemper is directly virus induced, since there is a clear correlation between the occurrence of demyelination and CDV replication in the cells of the white matter. Yet, there is little evidence for oligodendroglial infection. Changes of these cells have been reported in vitro and in vivo. The in vitro studies showed that – in contrast to other cells such as astrocytes and macrophages – oligodendrocytes hardly express CDV protein. However, we could show that these cells underwent a restricted infection with transcription of CDV RNA and that this phenomenon correlated with down-regulation of myelin gene transcription. The extension of these in vitro findings in vivo was obscured by the lack of reliable oligodendrocyte labelling techniques in canine brain tissue sections. In this study we combined immunohistochemistry with in situ hybridization to examine oligodendrocytes in demyelinating lesions and to investigate the question of oligodendrocyte infection in vivo. We could demonstrate that CDV infection leads to massive down-regulation of myelin gene expression in demyelinating lesions and that this effect correlates in part with a restricted infection of oligodendrocytes. Springer-Verlag 1997 /pmc/articles/PMC7086659/ /pubmed/9452824 http://dx.doi.org/10.1007/s004010050767 Text en © Springer-Verlag Berlin Heidelberg 1998 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
Zurbriggen, A.
Schmid, I.
Graber, H. U.
Vandevelde, M.
Oligodendroglial pathology in canine distemper
title Oligodendroglial pathology in canine distemper
title_full Oligodendroglial pathology in canine distemper
title_fullStr Oligodendroglial pathology in canine distemper
title_full_unstemmed Oligodendroglial pathology in canine distemper
title_short Oligodendroglial pathology in canine distemper
title_sort oligodendroglial pathology in canine distemper
topic Regular Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7086659/
https://www.ncbi.nlm.nih.gov/pubmed/9452824
http://dx.doi.org/10.1007/s004010050767
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