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Viral-mediated oligodendroglial alpha-synuclein expression models multiple system atrophy.

Identifieur interne : 000065 ( Main/Exploration ); précédent : 000064; suivant : 000066

Viral-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 :

RBID : pubmed:28556404

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:


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<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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