Neuroprotective effect of a CNTF-expressing lentiviral vector in the quinolinic acid rat model of Huntington's disease.

Détails

ID Serval
serval:BIB_67681C717613
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
Neuroprotective effect of a CNTF-expressing lentiviral vector in the quinolinic acid rat model of Huntington's disease.
Périodique
Neurobiology of Disease
Auteur⸱e⸱s
de Almeida L.P., Zala D., Aebischer P., Déglon N.
ISSN
0969-9961 (Print)
ISSN-L
0969-9961
Statut éditorial
Publié
Date de publication
2001
Volume
8
Numéro
3
Pages
433-446
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov'tPublication Status: ppublish
Résumé
Neurodegenerative diseases represent promising targets for gene therapy approaches provided effective transfer vectors. In the present study, we evaluated the effectiveness of LacZ-expressing lentiviral vectors with two different internal promoters, the mouse phosphoglycerate kinase 1 (PGK) and cytomegalovirus (CMV), to infect striatal cells. The intrastriatal injection of lenti-beta-Gal vectors lead to 207, 400 +/- 11,500 and 303,100 +/- 4,300 infected cells in adult rats, respectively. Importantly, the beta-galactosidase activity was higher in striatal extracts from PGK-LacZ-injected animals as compared to CMV-LacZ animals. The efficacy of the system was further examined with a potential therapeutic gene for the treatment of Huntington's disease, the human ciliary neurotrophic factor (CNTF). PGK-LacZ- or PGK-CNTF-expressing viruses were stereotaxically injected into the striatum of rats, 3 weeks later the animals were unilaterally lesioned with 180 nmol of quinolinic acid (QA). Control animals displayed 148 +/- 43 apomorphine-induced rotations ipsilateral to the lesion 5 days postlesion as compared to 26 +/- 22 turns/45 min in the CNTF-treated group. The extent of the striatal damage was significantly diminished in the CNTF-treated rats as indicated by the 52 +/- 9.7% decrease of the lesion volume and the sparing of DARPP-32, ChAT and NADPH-d neuronal populations. These results further establish that lentiviruses may represent an efficient gene delivery system for the screening of therapeutic molecules in Huntington's disease.
Mots-clé
Animals, Ciliary Neurotrophic Factor/genetics, Cytomegalovirus/genetics, Disease Models, Animal, Female, Gene Expression, Gene Therapy/methods, Genetic Vectors, Huntington Disease/chemically induced, Huntington Disease/therapy, Lentivirus/genetics, Neuroprotective Agents, Phosphoglycerate Kinase/genetics, Promoter Regions, Genetic, Quinolinic Acid, Rats, Rats, Wistar, beta-Galactosidase/genetics
Pubmed
Web of science
Création de la notice
13/12/2011 17:38
Dernière modification de la notice
20/08/2019 15:22
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