Enhanced Efficacy of the CDNF/MANF Family by Combined Intranigral Overexpression in the 6-OHDA Rat Model of Parkinson's Disease

被引:70
作者
Cordero-Llana, Oscar [1 ]
Houghton, Benjamin C. [1 ]
Rinaldi, Federica [1 ]
Taylor, Hannah [1 ]
Yanez-Munoz, Rafael J. [2 ]
Uney, James B. [1 ,3 ]
Wong, Liang-Fong [1 ,3 ]
Caldwell, Maeve A. [1 ,3 ]
机构
[1] Sch Clin Sci, Bristol BS8 1TD, Avon, England
[2] Univ London, Sch Biol Sci, Egham, Surrey, England
[3] Regenerat Med Lab, Bristol, Avon, England
基金
英国生物技术与生命科学研究理事会;
关键词
NIGROSTRIATAL DOPAMINE SYSTEM; DEFICIENT LENTIVIRAL VECTORS; NEUROTROPHIC FACTOR; GENE-THERAPY; CONTROLLED-TRIAL; CDNF PROTECTS; DOUBLE-BLIND; IN-VIVO; DELIVERY; NEURONS;
D O I
10.1038/mt.2014.206
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
Cerebral Dopamine Neurotrophic Factor (CDNF) and Mesencephalic Astrocyte-derived Neurotrophic factor (MANF) are members of a recently discovered family of neurotrophic factors (NTFs). Here, we used intranigral or intrastriatal lentiviral vector-mediated expression to evaluate their efficacy at protecting dopaminergic function in the 6-OHDA model of Parkinson's disease (PD). In contrast to the well-studied Glial-Derived Neurotrophic Factor (GDNF), no beneficial effects were demonstrated by striatal overexpression of either protein. Interestingly, nigral overexpression of CDNF decreased amphetamine-induced rotations and increased tyroxine hydroxylase (TH) striatal fiber density but had no effect on numbers of TH+ cells in the SN. Nigral MANF overexpression had no effect on amphetamine-induced rotations or TH striatat fiber density but resulted in a significant preservation of TH+ cells. Combined nigral overexpression of both factors led to a robust reduction in amphetamine-induced rotations, greater increase in striatal TH-fiber density and significant protection of TH+ cells in the SN. We conclude that nigral CDNF and MANF delivery is more efficacious than striatal delivery. This is also the first study to demonstrate that combined NTF can have synergistic effects that result in enhanced neuroprotection, suggesting that multiple NTF delivery may be more efficacious for the treatment of PD than the single NTF approaches attempted so far.
引用
收藏
页码:244 / 254
页数:11
相关论文
共 42 条
[1]
The GDNF family: Signalling, biological functions and therapeutic value [J].
Airaksinen, MS ;
Saarma, M .
NATURE REVIEWS NEUROSCIENCE, 2002, 3 (05) :383-394
[2]
CDNF Protects the Nigrostriatal Dopamine System and Promotes Recovery After MPTP Treatment in Mice [J].
Airavaara, Mikko ;
Harvey, Brandon K. ;
Voutilainen, Merja H. ;
Shen, Hui ;
Chou, Jenny ;
Lindholm, Paivi ;
Lindahl, Maria ;
Tuominen, Raimo K. ;
Saarma, Mart ;
Hoffer, Barry ;
Wang, Yun .
CELL TRANSPLANTATION, 2012, 21 (06) :1213-1223
[3]
Gene therapy with AAV2-CDNF provides functional benefits in a rat model of Parkinson's disease [J].
Back, Susanne ;
Peranen, Johan ;
Galli, Emilia ;
Pulkkila, Paivi ;
Lonka-Nevalaita, Liina ;
Tamminen, Tuulia ;
Voutilainen, Merja H. ;
Raasmaja, Atso ;
Saarma, Mart ;
Mannisto, Pekka T. ;
Tuominen, Raimo K. .
BRAIN AND BEHAVIOR, 2013, 3 (02) :75-88
[4]
Clinical Progression in Parkinson Disease and the Neurobiology of Axons [J].
Cheng, Hsiao-Chun ;
Ulane, Christina M. ;
Burke, Robert E. .
ANNALS OF NEUROLOGY, 2010, 67 (06) :715-725
[5]
Lentiviral-mediated transfer of CDNF promotes nerve regeneration and functional recovery after sciatic nerve injury in adult rats [J].
Cheng, Lei ;
Liu, Yi ;
Zhao, Hua ;
Zhang, Wen ;
Guo, Ying-Jun ;
Nie, Lin .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2013, 440 (02) :330-335
[6]
Galanin promotes neuronal differentiation from neural progenitor cells in vitro and contributes to the generation of new olfactory neurons in the adult mouse brain [J].
Cordero-Llana, Oscar ;
Rinaldi, Federica ;
Brennan, Peter A. ;
Wynick, David ;
Caldwell, Maeve A. .
EXPERIMENTAL NEUROLOGY, 2014, 256 :93-104
[7]
GDNF fails to exert neuroprotection in a rat α-synuclein model of Parkinson's disease [J].
Decressac, Mickael ;
Ulusoy, Ayse ;
Mattsson, Bengt ;
Georgievska, Biljana ;
Romero-Ramos, Marina ;
Kirik, Deniz ;
Bjorklund, Anders .
BRAIN, 2011, 134 :2302-2311
[8]
Neurotrophic factors as a therapeutic target for Parkinson's disease [J].
Evans, Jonathan R. ;
Barker, Roger A. .
EXPERT OPINION ON THERAPEUTIC TARGETS, 2008, 12 (04) :437-447
[9]
AAV2 - mediated delivery of human neurturin to the rat nigrostriatal system: Long-term efficacy and tolerability of CERE-120 for Parkinson's disease [J].
Gasmi, Mehdi ;
Brandon, Eugene P. ;
Herzoga, Christopher D. ;
Wilson, Alistair ;
Bishop, Kathie M. ;
Hofer, Eva K. ;
Cunningham, Justine J. ;
Printz, Marie A. ;
Kordower, Jeffrey H. ;
Bartus, Raymond T. .
NEUROBIOLOGY OF DISEASE, 2007, 27 (01) :67-76
[10]
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