GDNF fails to exert neuroprotection in a rat α-synuclein model of Parkinson's disease

被引:152
作者
Decressac, Mickael [1 ]
Ulusoy, Ayse [2 ]
Mattsson, Bengt [1 ]
Georgievska, Biljana [1 ]
Romero-Ramos, Marina [2 ]
Kirik, Deniz [2 ]
Bjorklund, Anders [1 ]
机构
[1] Wallenberg Neurosci Ctr, S-22184 Lund, Sweden
[2] Lund Univ, Dept Expt Med Sci Brain Repair & Imaging Neural S, S-22184 Lund, Sweden
基金
瑞典研究理事会;
关键词
Parkinson's disease; alpha-synuclein; GDNF; lentiviral vector; adeno-associated viral vector; NEUROTROPHIC FACTOR; GENE-TRANSFER; TYROSINE-HYDROXYLASE; STRIATAL DELIVERY; DOWN-REGULATION; OVEREXPRESSION; NEURONS; NEURODEGENERATION; DEGENERATION; INFUSION;
D O I
10.1093/brain/awr149
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
The neuroprotective effect of the glial cell line-derived neurotrophic factor has been extensively studied in various toxic models of Parkinson's disease. However, it remains unclear whether this neurotrophic factor can protect against the toxicity induced by the aggregation-prone protein alpha-synuclein. Targeted overexpression of human wild-type alpha-synuclein in the nigrostriatal system, using adeno-associated viral vectors, causes a progressive degeneration of the nigral dopamine neurons and the development of axonal pathology in the striatum. In the present study, we investigated, using different paradigms of delivery, whether glial cell line-derived neurotrophic factor can protect against the neurodegenerative changes and the cellular stress induced by alpha-synuclein. We found that viral vector-mediated delivery of glial cell line-derived neurotrophic factor into substantia nigra and/or striatum, administered 2-3 weeks before alpha-synuclein, was inefficient in preventing the wild-type alpha-synuclein-induced loss of dopamine neurons and terminals. In addition, glial cell line-derived neurotrophic factor overexpression did not ameliorate the behavioural deficit in this rat model of Parkinson's disease. Quantification of striatal alpha-synuclein-positive aggregates revealed that glial cell line-derived neurotrophic factor had no effect on alpha-synuclein aggregation. These data provide the evidence for the lack of neuroprotective effect of glial cell line-derived neurotrophic factor against the toxicity of human wild-type alpha-synuclein in an in vivo model of Parkinson's disease. The difference in neuroprotective efficacy of glial cell line-derived neurotrophic factor seen in our model and the commonly used neurotoxin models of Parkinson's disease, raises important issues pertinent to the interpretation of the results obtained in preclinical models of Parkinson's disease, and their relevance for the therapeutic use glial cell line-derived neurotrophic factor in patients with Parkinson's disease.
引用
收藏
页码:2302 / 2311
页数:10
相关论文
共 34 条
[1]
Repairing the parkinsonian brain with neurotrophic factors [J].
Aron, Liviu ;
Klein, Ruediger .
TRENDS IN NEUROSCIENCES, 2011, 34 (02) :88-100
[2]
Bioactivity of AAV2-Neurturin Gene Therapy (CERE-120): Differences Between Parkinson's Disease and Nonhuman Primate Brains [J].
Bartus, Raymond T. ;
Herzog, Christopher D. ;
Chu, Yaping ;
Wilson, Alistair ;
Brown, Lamar ;
Siffert, Joao ;
Johnson, Eugene M., Jr. ;
Olanow, C. Warren ;
Mufson, Elliott J. ;
Kordower, Jeffrey H. .
MOVEMENT DISORDERS, 2011, 26 (01) :27-36
[3]
Towards a neuroprotective gene therapy for Parkinson's disease:: use of adenovirus, AAV and lentivirus vectors for gene transfer of GDNF to the nigrostriatal system in the rat Parkinson model [J].
Björklund, A ;
Kirik, D ;
Rosenblad, C ;
Georgievska, B ;
Lundberg, C ;
Mandel, RJ .
BRAIN RESEARCH, 2000, 886 (1-2) :82-98
[4]
Dynamic Changes in Presynaptic and Axonal Transport Proteins Combined with Striatal Neuroinflammation Precede Dopaminergic Neuronal Loss in a Rat Model of AAV α-Synucleinopathy [J].
Chung, Chee Yeun ;
Koprich, James B. ;
Siddiqi, Hasan ;
Isacson, Ole .
JOURNAL OF NEUROSCIENCE, 2009, 29 (11) :3365-3373
[5]
Striatal delivery of neurturin by CERE-120, an AAV2 vector for the treatment of dopaminergic neuron degeneration in Parkinson's disease [J].
Gasmi, Mehdi ;
Herzog, Christopher D. ;
Brandon, Eugene P. ;
Cunningham, Justine J. ;
Ramirez, G. Anthony ;
Ketchum, Elias T. ;
Bartus, Raymond T. .
MOLECULAR THERAPY, 2007, 15 (01) :62-68
[6]
Overexpression of glial cell line-derived neurotrophic factor using a lentiviral vector induces time-and dose-dependent downregulation of tyrosine hydroxylase in the intact nigrostriatal dopamine system [J].
Georgievska, B ;
Kirik, D ;
Björklund, A .
JOURNAL OF NEUROSCIENCE, 2004, 24 (29) :6437-6445
[7]
Neuroprotection in the rat Parkinson model by intrastriatal GDNF gene transfer using a lentiviral vector [J].
Georgievska, B ;
Kirik, D ;
Rosenblad, C ;
Lundberg, C ;
Björklund, A .
NEUROREPORT, 2002, 13 (01) :75-82
[8]
Aberrant sprouting and downregulation of tyrosine hydroxylase in lesioned nigrostriatal dopamine neurons induced by long-lasting overexpression of glial cell line derived neurotrophic factor in the striatum by lentiviral gene transfer [J].
Georgievska, B ;
Kirik, D ;
Björklund, A .
EXPERIMENTAL NEUROLOGY, 2002, 177 (02) :461-474
[9]
Direct brain infusion of glial cell line-derived neurotrophic factor in Parkinson disease [J].
Gill, SS ;
Patel, NK ;
Hotton, GR ;
O'Sullivan, K ;
McCarter, R ;
Bunnage, M ;
Brooks, DJ ;
Svendsen, CN ;
Heywood, P .
NATURE MEDICINE, 2003, 9 (05) :589-595
[10]
Production methods for gene transfer vectors based on adeno-associated virus serotypes [J].
Grimm, D .
METHODS, 2002, 28 (02) :146-157