| Literature DB >> 28730349 |
Mayuko Y Kumasaka1,2,3, Ichiro Yajima1,2,3, Nobutaka Ohgami1,2,3, Hiromasa Ninomiya1,3, Machiko Iida1,2,3, Xiang Li1, Reina Oshino1,3, Hiroko Tanihata1, Masafumi Yoshinaga1,3, Masashi Kato4,5,6.
Abstract
Previous studies showed that overexposure to manganese causes parkinsonism, a disorder of dopaminergic neurons. Previous studies also showed that activity of c-RET kinase controls dopamine production through regulation of tyrosine hydroxylase (TH) expression, suggesting the involvement of c-RET in the development of parkinsonism. To our knowledge, however, there is no report showing a correlation between manganese-mediated parkinsonism and c-RET. In this study, we examined the effect of manganese on the expression and/or activation levels of c-RET and TH in human TH-expressing cells (TGW cells). We first found that treatment with 30 and 100 μM manganese resulted in reduction of c-RET transcript level and degradation of c-RET protein through promotion of ubiquitination. We then examined the biological significance of manganese-mediated decrease of c-RET protein expression. Decreased TH expression with decreased c-RET kinase activity was observed in c-RET protein-depleted TGW cells by treatment with manganese (30 μM) as well as by c-RET siRNA transfection. Since TH protein has been shown to be involved in the dopamine-producing pathway in previous studies, our results indicate the possibility that manganese-mediated reduction of TH expression and phosphorylation via decreased expression of c-RET protein in neural cells is involved in parkinsonism induced by manganese.Entities:
Keywords: Manganese; Metals; Protein expression; RET; Tyrosine kinase
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Year: 2017 PMID: 28730349 DOI: 10.1007/s12640-017-9783-0
Source DB: PubMed Journal: Neurotox Res ISSN: 1029-8428 Impact factor: 3.911