Neuroprotective Transcription Factors in Animal Models of Parkinson Disease

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 feature...

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Main Authors: François-Xavier Blaudin de Thé, Hocine Rekaik, Alain Prochiantz, Julia Fuchs, Rajiv L. Joshi
Format: Article
Language:English
Published: Hindawi Limited 2016-01-01
Series:Neural Plasticity
Online Access:http://dx.doi.org/10.1155/2016/6097107
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spelling doaj-bf32e04f1e9741b1acdcbdfeea52f41b2020-11-24T23:52:08ZengHindawi LimitedNeural Plasticity2090-59041687-54432016-01-01201610.1155/2016/60971076097107Neuroprotective Transcription Factors in Animal Models of Parkinson DiseaseFrançois-Xavier Blaudin de Thé0Hocine Rekaik1Alain Prochiantz2Julia Fuchs3Rajiv L. Joshi4Center for Interdisciplinary Research in Biology (CIRB), Labex Memolife, CNRS UMR 7241, INSERM U1050, Collège de France, 11 place Marcelin Berthelot, 75231 Paris Cedex 05, FranceCenter for Interdisciplinary Research in Biology (CIRB), Labex Memolife, CNRS UMR 7241, INSERM U1050, Collège de France, 11 place Marcelin Berthelot, 75231 Paris Cedex 05, FranceCenter for Interdisciplinary Research in Biology (CIRB), Labex Memolife, CNRS UMR 7241, INSERM U1050, Collège de France, 11 place Marcelin Berthelot, 75231 Paris Cedex 05, FranceCenter for Interdisciplinary Research in Biology (CIRB), Labex Memolife, CNRS UMR 7241, INSERM U1050, Collège de France, 11 place Marcelin Berthelot, 75231 Paris Cedex 05, FranceCenter for Interdisciplinary Research in Biology (CIRB), Labex Memolife, CNRS UMR 7241, INSERM U1050, Collège de France, 11 place Marcelin Berthelot, 75231 Paris Cedex 05, FranceA 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.http://dx.doi.org/10.1155/2016/6097107
collection DOAJ
language English
format Article
sources DOAJ
author François-Xavier Blaudin de Thé
Hocine Rekaik
Alain Prochiantz
Julia Fuchs
Rajiv L. Joshi
spellingShingle François-Xavier Blaudin de Thé
Hocine Rekaik
Alain Prochiantz
Julia Fuchs
Rajiv L. Joshi
Neuroprotective Transcription Factors in Animal Models of Parkinson Disease
Neural Plasticity
author_facet François-Xavier Blaudin de Thé
Hocine Rekaik
Alain Prochiantz
Julia Fuchs
Rajiv L. Joshi
author_sort François-Xavier Blaudin de Thé
title Neuroprotective Transcription Factors in Animal Models of Parkinson Disease
title_short Neuroprotective Transcription Factors in Animal Models of Parkinson Disease
title_full Neuroprotective Transcription Factors in Animal Models of Parkinson Disease
title_fullStr Neuroprotective Transcription Factors in Animal Models of Parkinson Disease
title_full_unstemmed Neuroprotective Transcription Factors in Animal Models of Parkinson Disease
title_sort neuroprotective transcription factors in animal models of parkinson disease
publisher Hindawi Limited
series Neural Plasticity
issn 2090-5904
1687-5443
publishDate 2016-01-01
description 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.
url http://dx.doi.org/10.1155/2016/6097107
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