| Title | S -Nitrosoglutathione Reductase Plays Opposite Roles in SH-SY5Y Models of Parkinson's Disease and Amyotrophic Lateral Sclerosis |
|---|---|
| Publication Type | Articolo su Rivista peer-reviewed |
| Year of Publication | 2015 |
| Authors | Rizza, S., Cirotti C., Montagna C., Cardaci S., Consales Claudia, Cozzolino M., Carrì M.T., Cecconi F., and Filomeni G. |
| Journal | Mediators of Inflammation |
| Volume | 2015 |
| ISSN | 09629351 |
| Keywords | amyotrophic lateral sclerosis, animal experiment, animal model, article, cell death, cell protection, cell viability, cellular distribution, controlled study, disease severity, DJ 1 protein, gene silencing, glutathione reductase, human, human cell, in vitro study, mouse, nerve cell, nerve degeneration, nitrosative stress, nitrosylation, nonhuman, Oxidative stress, Parkinson disease, Phenotype, protein expression, protein function, receptor down regulation, s nitrosoglutathione reductase, transcription factor Nrf2, unclassified drug, upregulation |
| Abstract | Oxidative and nitrosative stresses have been reported as detrimental phenomena concurring to the onset of several neurodegenerative diseases. Here we reported that the ectopic modulation of the denitrosylating enzyme S-nitrosoglutathione reductase (GSNOR) differently impinges on the phenotype of two SH-SY5Y-based in vitro models of neurodegeneration, namely, Parkinson's disease (PD) and familial amyotrophic lateral sclerosis (fALS). In particular, we provide evidence that GSNOR-knocking down protects SH-SY5Y against PD toxins, while, by contrast, its upregulation is required for G93A-SOD1 expressing cells resistance to NO-releasing drugs. Although completely opposite, both conditions are characterized by Nrf2 localization in the nuclear compartment: in the first case induced by GSNOR silencing, while in the second one underlying the antinitrosative response. Overall, our results demonstrate that GSNOR expression has different effect on neuronal viability in dependence on the stimulus applied and suggest that GSNOR could be a responsive gene downstream of Nrf2 activation. © 2015 Salvatore Rizza et al. |
| Notes | cited By 0 |
| URL | https://www.scopus.com/inward/record.uri?eid=2-s2.0-84944191410&doi=10.1155%2f2015%2f536238&partnerID=40&md5=f2c928c177f398ca73c2eb19c73b2f22 |
| DOI | 10.1155/2015/536238 |
| Citation Key | Rizza2015 |
