Serveur d'exploration Covid

Attention, ce site est en cours de développement !
Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.

Demyelination in canine distemper encephalomyelitis: An ultrastructural analysis

Identifieur interne : 001584 ( Main/Exploration ); précédent : 001583; suivant : 001585

Demyelination in canine distemper encephalomyelitis: An ultrastructural analysis

Auteurs : Brian A. Sumummers [États-Unis] ; Max J. G. Appel [États-Unis]

Source :

RBID : ISTEX:DA4530BFA28CD375BC4D62681FDDE9CE9D123171

English descriptors

Abstract

Summary: A morphological study of selected white matter lesions was carried out in three dogs with canine distemper encephalomyelitis. Two dogs had experimental infections while the third was a spontaneous case. Two stages were identified in the process of demyelination. The earliest evidence of myelin injury was a ballooning change in myelin sheaths involving single or multiple axons. This was followed by a progressive stripping of compact sheaths by the cytoplasmic fingers of phagocytic cells which infiltrated and removed myelin lamellae. Some axonal necrosis also accompanied these changes. Where demyelination occurred, canine distemper viral nucleocapsids were found in astrocytes, macrophages, ependymal cells and infiltrating lymphocytes. In contrast, oligodendrocytes were conspicuous by their apparent lack of infection. Thus it seems that myelin loss cannot be ascribed to oligodendrocyte infection. Perturbed astrocyte function following canine distemper viral infection may cause oedema of myelin sheaths, leading to ballooning and primary demyelination. Cells which phagocytosed myelin were mainly identified as microglial cells with lesser involvement by astrocytes. Rarely, oligodendrocytes also acted as macrophages. Myelin debris was engulfed in bulk or as small droplets into coated pits. Remyelination was present in established plaques although not in great abundance, perhaps due to the diminished oligodendrocyte numbers and a relative increase in immature forms of these cells. These observations are compared to similar changes observed in other demyelinating diseases of animals and man.

Url:
DOI: 10.1007/BF01611991


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

<record>
<TEI wicri:istexFullTextTei="biblStruct">
<teiHeader>
<fileDesc>
<titleStmt>
<title xml:lang="en">Demyelination in canine distemper encephalomyelitis: An ultrastructural analysis</title>
<author>
<name sortKey="Sumummers, Brian A" sort="Sumummers, Brian A" uniqKey="Sumummers B" first="Brian A." last="Sumummers">Brian A. Sumummers</name>
</author>
<author>
<name sortKey="Appel, Max J G" sort="Appel, Max J G" uniqKey="Appel M" first="Max J. G." last="Appel">Max J. G. Appel</name>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:DA4530BFA28CD375BC4D62681FDDE9CE9D123171</idno>
<date when="1987" year="1987">1987</date>
<idno type="doi">10.1007/BF01611991</idno>
<idno type="url">https://api.istex.fr/ark:/67375/1BB-C8FCQ2RT-C/fulltext.pdf</idno>
<idno type="wicri:Area/Istex/Corpus">000582</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">000582</idno>
<idno type="wicri:Area/Istex/Curation">000562</idno>
<idno type="wicri:Area/Istex/Checkpoint">000722</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Checkpoint">000722</idno>
<idno type="wicri:doubleKey">0300-4864:1987:Sumummers B:demyelination:in:canine</idno>
<idno type="wicri:Area/Main/Merge">001607</idno>
<idno type="wicri:Area/Main/Curation">001584</idno>
<idno type="wicri:Area/Main/Exploration">001584</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title level="a" type="main" xml:lang="en">Demyelination in canine distemper encephalomyelitis: An ultrastructural analysis</title>
<author>
<name sortKey="Sumummers, Brian A" sort="Sumummers, Brian A" uniqKey="Sumummers B" first="Brian A." last="Sumummers">Brian A. Sumummers</name>
<affiliation wicri:level="4">
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Pathology, New York State College of Veterinary Medicine, Cornell University, 14853, Ithaca, NY</wicri:regionArea>
<placeName>
<region type="state">État de New York</region>
<settlement type="city">Ithaca (New York)</settlement>
</placeName>
<orgName type="university">Université Cornell</orgName>
</affiliation>
</author>
<author>
<name sortKey="Appel, Max J G" sort="Appel, Max J G" uniqKey="Appel M" first="Max J. G." last="Appel">Max J. G. Appel</name>
<affiliation wicri:level="4">
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Microbiology (James A. Baker Institute), New York State College of Veterinary Medicine, Cornell University, 14853, Ithaca, NY</wicri:regionArea>
<placeName>
<region type="state">État de New York</region>
<settlement type="city">Ithaca (New York)</settlement>
</placeName>
<orgName type="university">Université Cornell</orgName>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series>
<title level="j">Journal of Neurocytology</title>
<title level="j" type="abbrev">J Neurocytol</title>
<idno type="ISSN">0300-4864</idno>
<idno type="eISSN">1573-7381</idno>
<imprint>
<publisher>Kluwer Academic Publishers</publisher>
<pubPlace>Dordrecht</pubPlace>
<date type="published" when="1987-12-01">1987-12-01</date>
<biblScope unit="volume">16</biblScope>
<biblScope unit="issue">6</biblScope>
<biblScope unit="page" from="871">871</biblScope>
<biblScope unit="page" to="881">881</biblScope>
</imprint>
<idno type="ISSN">0300-4864</idno>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt>
<idno type="ISSN">0300-4864</idno>
</seriesStmt>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="Teeft" xml:lang="en">
<term>Acta</term>
<term>Acta neuropathologica</term>
<term>Appel</term>
<term>Astrocyte</term>
<term>Astroglial</term>
<term>Axon</term>
<term>Ballooning</term>
<term>Brain research</term>
<term>Canine</term>
<term>Canine distemper</term>
<term>Canine distemper encephalomyelitis</term>
<term>Demyelinated</term>
<term>Demyelinated axons</term>
<term>Demyelinating</term>
<term>Demyelinating diseases</term>
<term>Demyelinating lesions</term>
<term>Demyelination</term>
<term>Distemper</term>
<term>Distemper virus</term>
<term>Electron microscopy</term>
<term>Encephalomyelitis</term>
<term>Endoplasmic</term>
<term>Endoplasmic reticulum</term>
<term>Ependymal cells</term>
<term>Fibre</term>
<term>Higgins</term>
<term>Hypertrophic astrocytes</term>
<term>Inflammatory</term>
<term>Intraperiod line</term>
<term>Laboratory investigation</term>
<term>Lesion</term>
<term>Lymphocyte</term>
<term>Macrophage</term>
<term>Microglia</term>
<term>Microglial</term>
<term>Microglial cell</term>
<term>Microglial cells</term>
<term>Mori leblond</term>
<term>Multiple sclerosis</term>
<term>Myelin</term>
<term>Myelin ballooning</term>
<term>Myelin loss</term>
<term>Myelin phagocytosis</term>
<term>Myelin sheath</term>
<term>Myelin sheaths</term>
<term>Naked axons</term>
<term>Neurological sciences</term>
<term>Neurology</term>
<term>Neuropathologica</term>
<term>Oligodendrocyte</term>
<term>Oligodendrocyte infection</term>
<term>Perivascular</term>
<term>Plaque</term>
<term>Primary demyelination</term>
<term>Raine</term>
<term>Remyelination</term>
<term>Reticulum</term>
<term>Rough endoplasmic reticulum</term>
<term>Sclerosis</term>
<term>Sheath</term>
<term>Spinal cord</term>
<term>Spontaneous case</term>
<term>Tubuloreticular inclusions</term>
<term>Ultrastructural</term>
<term>Viral</term>
<term>Virus encephalomyelitis</term>
<term>White matter</term>
<term>White matter lesions</term>
<term>Wisniewski</term>
</keywords>
</textClass>
<langUsage>
<language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">Summary: A morphological study of selected white matter lesions was carried out in three dogs with canine distemper encephalomyelitis. Two dogs had experimental infections while the third was a spontaneous case. Two stages were identified in the process of demyelination. The earliest evidence of myelin injury was a ballooning change in myelin sheaths involving single or multiple axons. This was followed by a progressive stripping of compact sheaths by the cytoplasmic fingers of phagocytic cells which infiltrated and removed myelin lamellae. Some axonal necrosis also accompanied these changes. Where demyelination occurred, canine distemper viral nucleocapsids were found in astrocytes, macrophages, ependymal cells and infiltrating lymphocytes. In contrast, oligodendrocytes were conspicuous by their apparent lack of infection. Thus it seems that myelin loss cannot be ascribed to oligodendrocyte infection. Perturbed astrocyte function following canine distemper viral infection may cause oedema of myelin sheaths, leading to ballooning and primary demyelination. Cells which phagocytosed myelin were mainly identified as microglial cells with lesser involvement by astrocytes. Rarely, oligodendrocytes also acted as macrophages. Myelin debris was engulfed in bulk or as small droplets into coated pits. Remyelination was present in established plaques although not in great abundance, perhaps due to the diminished oligodendrocyte numbers and a relative increase in immature forms of these cells. These observations are compared to similar changes observed in other demyelinating diseases of animals and man.</div>
</front>
</TEI>
<affiliations>
<list>
<country>
<li>États-Unis</li>
</country>
<region>
<li>État de New York</li>
</region>
<settlement>
<li>Ithaca (New York)</li>
</settlement>
<orgName>
<li>Université Cornell</li>
</orgName>
</list>
<tree>
<country name="États-Unis">
<region name="État de New York">
<name sortKey="Sumummers, Brian A" sort="Sumummers, Brian A" uniqKey="Sumummers B" first="Brian A." last="Sumummers">Brian A. Sumummers</name>
</region>
<name sortKey="Appel, Max J G" sort="Appel, Max J G" uniqKey="Appel M" first="Max J. G." last="Appel">Max J. G. Appel</name>
</country>
</tree>
</affiliations>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Sante/explor/CovidV1/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 001584 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 001584 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Sante
   |area=    CovidV1
   |flux=    Main
   |étape=   Exploration
   |type=    RBID
   |clé=     ISTEX:DA4530BFA28CD375BC4D62681FDDE9CE9D123171
   |texte=   Demyelination in canine distemper encephalomyelitis: An ultrastructural analysis
}}

Wicri

This area was generated with Dilib version V0.6.33.
Data generation: Fri Mar 27 18:14:15 2020. Site generation: Sun Jan 31 15:15:08 2021