| Literature DB >> 29486298 |
Nicoletta Rizzi1, Electra Brunialti1, Silvia Cerri2, Greta Cermisoni1, Giovanna Levandis2, Nicoletta Cesari3, Adriana Maggi1, Fabio Blandini2, Paolo Ciana4.
Abstract
The Parkinson's disease (PD) evolves over an extended period of time with the onset occurring long before clinical signs begin to manifest. Characterization of the molecular events underlying the PD onset is instrumental for the development of diagnostic markers and preventive treatments, progress in this field is hindered by technical limitations. We applied an imaging approach to demonstrate the activation of Nrf2 transcription factor as a hallmark of neurodegeneration in neurotoxin-driven models of PD. In dopaminergic SK-N-BE neuroblastoma cells, Nrf2 activation was detected in cells committed to die as proven by time lapse microscopy; in the substantia nigra pars compacta area of the mouse brain, the Nrf2 activation preceded dopaminergic neurodegeneration as demonstrated by in vivo and ex vivo optical imaging, a finding confirmed by co-localization experiments carried out by immunohistochemistry. Collectively, our results identify the Nrf2 signaling as an early marker of neurodegeneration, anticipating dopaminergic neurodegeneration and motor deficits.Entities:
Keywords: ARE-luc2 mouse; Anti-oxidant responsive elements; Bioluminescence; In vivo imaging; Nrf-2; Oxidative stress; Parkinson's disease; Reporter mouse
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Year: 2018 PMID: 29486298 DOI: 10.1016/j.nbd.2018.02.005
Source DB: PubMed Journal: Neurobiol Dis ISSN: 0969-9961 Impact factor: 5.996