Viral-mediated oligodendroglial alpha-synuclein expression models multiple system atrophy.
Identifieur interne : 000065 ( Main/Exploration ); précédent : 000064; suivant : 000066Viral-mediated oligodendroglial alpha-synuclein expression models multiple system atrophy.
Auteurs : Fares Bassil [France] ; Paul A. Guerin [France] ; Nathalie Dutheil [France] ; Qin Li [République populaire de Chine] ; Matthias Klugmann [Australie] ; Wassilios G. Meissner [France] ; Erwan Bezard [France] ; Pierre-Olivier Fernagut [France]Source :
- Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2017.
Abstract
MSA is a fatal neurodegenerative disorder characterized by a combination of autonomic dysfunction, cerebellar ataxia, and l-dopa unresponsive parkinsonism. The hallmark of MSA is the accumulation of α-synuclein, forming cytoplasmic inclusions in oligodendrocytes. Adeno-associated viruses allow efficient targeting of disease-associated genes in selected cellular ensembles and have proven efficient for the neuronal overexpression of α-synuclein in the substantia nigra in the context of PD.
DOI: 10.1002/mds.27041
PubMed: 28556404
Affiliations:
- Australie, France, République populaire de Chine
- Aquitaine, Nouvelle-Aquitaine
- Bordeaux, Pékin
- Université de Bordeaux
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Le document en format XML
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<front><div type="abstract" xml:lang="en">MSA is a fatal neurodegenerative disorder characterized by a combination of autonomic dysfunction, cerebellar ataxia, and l-dopa unresponsive parkinsonism. The hallmark of MSA is the accumulation of α-synuclein, forming cytoplasmic inclusions in oligodendrocytes. Adeno-associated viruses allow efficient targeting of disease-associated genes in selected cellular ensembles and have proven efficient for the neuronal overexpression of α-synuclein in the substantia nigra in the context of PD.</div>
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