Manganese-Mediated Decrease in Levels of c-RET and Tyrosine Hydroxylase Expression In Vitro

Neurotox Res. 2017 Nov;32(4):661-670. doi: 10.1007/s12640-017-9783-0. Epub 2017 Jul 20.

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.

Keywords: Manganese; Metals; Protein expression; RET; Tyrosine kinase.

MeSH terms

  • Dopamine / metabolism*
  • Humans
  • Manganese / metabolism*
  • Mesencephalon / metabolism
  • Neurons / drug effects
  • Phosphorylation / drug effects
  • Proto-Oncogene Proteins c-ret / metabolism*
  • Tyrosine 3-Monooxygenase / metabolism*

Substances

  • Manganese
  • Tyrosine 3-Monooxygenase
  • Proto-Oncogene Proteins c-ret
  • RET protein, human
  • Dopamine