Serveur d'exploration Chloroquine

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.

Pleomorphic mitochondrial and different filamentous inclusions in inflammatory myopathies associated with mtDNA deletions

Identifieur interne : 002800 ( Main/Exploration ); précédent : 002799; suivant : 002801

Pleomorphic mitochondrial and different filamentous inclusions in inflammatory myopathies associated with mtDNA deletions

Auteurs : M. Molnar [États-Unis] ; J. M. Schröder [États-Unis]

Source :

RBID : ISTEX:286DDA1F5267CB11B7B8B8B811BA346A39C39CA6

English descriptors

Abstract

Abstract: Mitochondrial changes are frequently observed in muscle fibers of patients with inclusion body myositis (IBM) and polymyositis (PM), suggesting that mitochondrial function may be especially impaired in these forms of inflammatory myopathies. Intranuclear and cytoplasmic tubulofilamentous inclusions are characteristic, although not totally specific for IBM. In the present cases, the inclusions were strikingly pleomorphic when chloroquine had been given for long periods. The nuclear inclusions were always tubular, whereas the cytoplasmic filaments had either a tubular, a helical, or a cross-striated structure with different diameters and arrangements in association with myelin-like figures, and vacuoles. Abnormal mitochondria containing paracrystalline, globoid, and other inclusions, noted in IBM, were occasionally also seen in PM or vasculitis. By contrast, in the latter, no intranuclear or cytoplasmic tubulofilamentous inclusions were apparent in muscle fibers. This study reports for the first time the presence of membrane-bound crystalloid inclusions in a muscle fiber with numerous abnormal mitochondria; similar structures have thus far only been observed in macrophages. The identity and function of these inclusions remains unknown. Using PCR analysis we detected different mtDNA deletions not only in IBM, but also in PM and vasculitis, indicating at least some degree of association between the structural mitochondrial abnormalities and the mtDNA mutations. There was no topographical correlation between the presence of tubular or helical filaments and the mitochondrial abnormalities. As already noted by others, the mitochondrial changes in IBM were more frequent than expected in this age group. It is suggested that the presence of the mtDNA deletions in IBM and PM are not primary, but rather the result of the underlying, presumably immunological disorder causing nuclear and secondary or simultaneous mitochondrial changes.

Url:
DOI: 10.1007/s004010050858


Affiliations:


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


Le document en format XML

<record>
<TEI wicri:istexFullTextTei="biblStruct">
<teiHeader>
<fileDesc>
<titleStmt>
<title xml:lang="en">Pleomorphic mitochondrial and different filamentous inclusions in inflammatory myopathies associated with mtDNA deletions</title>
<author>
<name sortKey="Molnar, M" sort="Molnar, M" uniqKey="Molnar M" first="M." last="Molnar">M. Molnar</name>
</author>
<author>
<name sortKey="Schroder, J M" sort="Schroder, J M" uniqKey="Schroder J" first="J. M." last="Schröder">J. M. Schröder</name>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">ISTEX</idno>
<idno type="RBID">ISTEX:286DDA1F5267CB11B7B8B8B811BA346A39C39CA6</idno>
<date when="1998" year="1998">1998</date>
<idno type="doi">10.1007/s004010050858</idno>
<idno type="url">https://api.istex.fr/ark:/67375/VQC-Z28LGRWP-0/fulltext.pdf</idno>
<idno type="wicri:Area/Istex/Corpus">000C18</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Corpus" wicri:corpus="ISTEX">000C18</idno>
<idno type="wicri:Area/Istex/Curation">000C18</idno>
<idno type="wicri:Area/Istex/Checkpoint">001604</idno>
<idno type="wicri:explorRef" wicri:stream="Istex" wicri:step="Checkpoint">001604</idno>
<idno type="wicri:doubleKey">0001-6322:1998:Molnar M:pleomorphic:mitochondrial:and</idno>
<idno type="wicri:Area/Main/Merge">002842</idno>
<idno type="wicri:Area/Main/Curation">002800</idno>
<idno type="wicri:Area/Main/Exploration">002800</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title level="a" type="main" xml:lang="en">Pleomorphic mitochondrial and different filamentous inclusions in inflammatory myopathies associated with mtDNA deletions</title>
<author>
<name sortKey="Molnar, M" sort="Molnar, M" uniqKey="Molnar M" first="M." last="Molnar">M. Molnar</name>
<affiliation wicri:level="2">
<country xml:lang="fr">États-Unis</country>
<placeName>
<region type="state">Delaware</region>
</placeName>
<wicri:cityArea>Institut für Neuropathologie, Universitätsklinikum der Rheinisch-Westfälischen Technischen Hochschule Aachen, Pauwelsstr. 30, D-52074 Aachen, Germany Tel.: 49-241-80 89428; Fax: 49-241-8888-416; e-mail: neupath@amsd.imib.rwth-aachen.de</wicri:cityArea>
</affiliation>
</author>
<author>
<name sortKey="Schroder, J M" sort="Schroder, J M" uniqKey="Schroder J" first="J. M." last="Schröder">J. M. Schröder</name>
<affiliation wicri:level="2">
<country xml:lang="fr">États-Unis</country>
<placeName>
<region type="state">Delaware</region>
</placeName>
<wicri:cityArea>Institut für Neuropathologie, Universitätsklinikum der Rheinisch-Westfälischen Technischen Hochschule Aachen, Pauwelsstr. 30, D-52074 Aachen, Germany Tel.: 49-241-80 89428; Fax: 49-241-8888-416; e-mail: neupath@amsd.imib.rwth-aachen.de</wicri:cityArea>
</affiliation>
</author>
</analytic>
<monogr></monogr>
<series>
<title level="j">Acta Neuropathologica</title>
<title level="j" type="abbrev">Acta Neuropathol</title>
<idno type="ISSN">0001-6322</idno>
<idno type="eISSN">1432-0533</idno>
<imprint>
<publisher>Springer-Verlag</publisher>
<pubPlace>Berlin/Heidelberg</pubPlace>
<date type="published" when="1998-06-01">1998-06-01</date>
<biblScope unit="volume">96</biblScope>
<biblScope unit="issue">1</biblScope>
<biblScope unit="page" from="41">41</biblScope>
<biblScope unit="page" to="51">51</biblScope>
</imprint>
<idno type="ISSN">0001-6322</idno>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt>
<idno type="ISSN">0001-6322</idno>
</seriesStmt>
</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="KwdEn" xml:lang="en">
<term>Crystalloid inclusion in macrophages</term>
<term>Key words Inclusion body myositis</term>
<term>Mitochondrial abnormalities</term>
<term>Polymyositis</term>
<term>mtDNA deletion</term>
</keywords>
</textClass>
<langUsage>
<language ident="en">en</language>
</langUsage>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">Abstract: Mitochondrial changes are frequently observed in muscle fibers of patients with inclusion body myositis (IBM) and polymyositis (PM), suggesting that mitochondrial function may be especially impaired in these forms of inflammatory myopathies. Intranuclear and cytoplasmic tubulofilamentous inclusions are characteristic, although not totally specific for IBM. In the present cases, the inclusions were strikingly pleomorphic when chloroquine had been given for long periods. The nuclear inclusions were always tubular, whereas the cytoplasmic filaments had either a tubular, a helical, or a cross-striated structure with different diameters and arrangements in association with myelin-like figures, and vacuoles. Abnormal mitochondria containing paracrystalline, globoid, and other inclusions, noted in IBM, were occasionally also seen in PM or vasculitis. By contrast, in the latter, no intranuclear or cytoplasmic tubulofilamentous inclusions were apparent in muscle fibers. This study reports for the first time the presence of membrane-bound crystalloid inclusions in a muscle fiber with numerous abnormal mitochondria; similar structures have thus far only been observed in macrophages. The identity and function of these inclusions remains unknown. Using PCR analysis we detected different mtDNA deletions not only in IBM, but also in PM and vasculitis, indicating at least some degree of association between the structural mitochondrial abnormalities and the mtDNA mutations. There was no topographical correlation between the presence of tubular or helical filaments and the mitochondrial abnormalities. As already noted by others, the mitochondrial changes in IBM were more frequent than expected in this age group. It is suggested that the presence of the mtDNA deletions in IBM and PM are not primary, but rather the result of the underlying, presumably immunological disorder causing nuclear and secondary or simultaneous mitochondrial changes.</div>
</front>
</TEI>
<affiliations>
<list>
<country>
<li>États-Unis</li>
</country>
<region>
<li>Delaware</li>
</region>
</list>
<tree>
<country name="États-Unis">
<region name="Delaware">
<name sortKey="Molnar, M" sort="Molnar, M" uniqKey="Molnar M" first="M." last="Molnar">M. Molnar</name>
</region>
<name sortKey="Schroder, J M" sort="Schroder, J M" uniqKey="Schroder J" first="J. M." last="Schröder">J. M. Schröder</name>
</country>
</tree>
</affiliations>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Sante/explor/ChloroquineV1/Data/Main/Exploration
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 002800 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd -nk 002800 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Sante
   |area=    ChloroquineV1
   |flux=    Main
   |étape=   Exploration
   |type=    RBID
   |clé=     ISTEX:286DDA1F5267CB11B7B8B8B811BA346A39C39CA6
   |texte=   Pleomorphic mitochondrial and different filamentous inclusions in inflammatory myopathies associated with mtDNA deletions
}}

Wicri

This area was generated with Dilib version V0.6.33.
Data generation: Wed Mar 25 22:43:59 2020. Site generation: Sun Jan 31 12:44:45 2021