Neuroprotective Transcription Factors in Animal Models of Parkinson Disease

被引:32
作者
de The, Francois-Xavier Blaudin [1 ]
Rekaik, Hocine [1 ]
Prochiantz, Alain [1 ]
Fuchs, Julia [1 ]
Joshi, Rajiv L. [1 ]
机构
[1] Coll France, INSERM U1050, CNRS UMR 7241, CIRB,Labex Memolife, 11 Pl Marcelin Berthelot, F-75231 Paris 05, France
基金
欧洲研究理事会;
关键词
MIDBRAIN DOPAMINERGIC-NEURONS; VENTRAL TEGMENTAL AREA; PITX3 GENE POLYMORPHISM; FACTOR 4E EIF4E; SUBSTANTIA-NIGRA; OTX2; HOMEOPROTEIN; RET EXPRESSION; SELECTIVE LOSS; DNA-DAMAGE; STEM-CELLS;
D O I
10.1155/2016/6097107
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
A number of transcription factors, including En1/2, Foxa1/2, Lmx1a/b, Nurr1, Otx2, and Pitx3, with key roles in midbrain dopaminergic (mDA) neuron development, also regulate adult mDA neuron survival and physiology. Mouse models with targeted disruption of some of these genes display several features reminiscent of Parkinson disease (PD), in particular the selective and progressive loss of mDA neurons in the substantia nigra pars compacta (SNpc). The characterization of these animal models has provided valuable insights into various mechanisms of PD pathogenesis. Therefore, the dissection of the mechanisms and survival signalling pathways engaged by these transcription factors to protect mDA neuron from degeneration can suggest novel therapeutic strategies. The work on En1/2-mediated neuroprotection also highlights the potential of protein transduction technology for neuroprotective approaches in PD.
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页数:11
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