In vitro models of multiple system atrophy
Identifieur interne :
001D72 ( PascalFrancis/Corpus );
précédent :
001D71;
suivant :
001D73
In vitro models of multiple system atrophy
Auteurs : Nadia Stefanova ;
Markus Reindl ;
Werner Poewe ;
Gregor K. WenningSource :
-
Movement disorders [ 0885-3185 ] ; 2005.
RBID : Pascal:05-0457543
Descripteurs français
English descriptors
Abstract
α-Synuclein represents the major constituent of oligodendroglial cytoplasmic inclusions, the hallmark lesion of multiple system atrophy (MSA), a progressive disorder that is associated with selective degenerative cell loss in basal ganglia, cerebellum, brainstem, and spinal cord. The role of abnormal α-synuclein aggregation in oligodendroglial cells is still obscure, in particular, whether α-synuclein might impair oligodendroglial and, secondarily, neuronal integrity of those cells in the diseased brain. In an attempt to answer some of these questions, we have developed an "in vitro model of MSA" by expressing the wild-type or C-terminally truncated form of α-synuclein in glial cell cultures. With this simplified system, we have demonstrated that α-synuclein significantly affects the survival of glia and its vulnerability to environmental stress, which might represent a major step in the pathogenesis of MSA.
Notice en format standard (ISO 2709)
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Format Inist (serveur)
NO : | PASCAL 05-0457543 INIST |
ET : | In vitro models of multiple system atrophy |
AU : | STEFANOVA (Nadia); REINDL (Markus); POEWE (Werner); WENNING (Gregor K.); POEWE (Werner); WENNING (Gregor K.) |
AF : | Neurological Research Laboratory, Department of Neurology, University Hospital of Innsbruck/Autriche (1 aut., 2 aut., 3 aut., 4 aut.); Department of Neurology, Medical University Innsbruck/Innsbruck/Autriche (1 aut., 2 aut.) |
DT : | Publication en série; Congrès; Niveau analytique |
SO : | Movement disorders; ISSN 0885-3185; Etats-Unis; Da. 2005; Vol. 20; No. SUP12; S53-S56; Bibl. 13 ref. |
LA : | Anglais |
EA : | α-Synuclein represents the major constituent of oligodendroglial cytoplasmic inclusions, the hallmark lesion of multiple system atrophy (MSA), a progressive disorder that is associated with selective degenerative cell loss in basal ganglia, cerebellum, brainstem, and spinal cord. The role of abnormal α-synuclein aggregation in oligodendroglial cells is still obscure, in particular, whether α-synuclein might impair oligodendroglial and, secondarily, neuronal integrity of those cells in the diseased brain. In an attempt to answer some of these questions, we have developed an "in vitro model of MSA" by expressing the wild-type or C-terminally truncated form of α-synuclein in glial cell cultures. With this simplified system, we have demonstrated that α-synuclein significantly affects the survival of glia and its vulnerability to environmental stress, which might represent a major step in the pathogenesis of MSA. |
CC : | 002B17; 002B17F; 002B17G |
FD : | Système nerveux pathologie; Atrophie multisystématisée; Modèle; Inclusion |
ED : | Nervous system diseases; Multiple system atrophy; Models; Inclusion |
SD : | Sistema nervioso patología; Atrofia multisistematizada; Modelo; Inclusión |
LO : | INIST-20953.354000132714250080 |
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