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Iron modulates the activity of monoamine oxidase B in SH-SY5Y cells.

Huiru LuJun ChenHui HuangMengxue ZhouQing ZhuShao Q YaoZhifang ChaiYi Hu
Published in: Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine (2017)
Both monoamine oxidase B (MAO-B) and iron accumulation are associated with neurologic diseases including Parkinson's disease. However, the association of iron with MAO-B activity was poorly understood. Here we took advantage of highly sensitive and specific fluorescence probes to examine the change in MAO-B activity in human dopaminergic neuroblastoma (SH-SY5Y) cells upon iron exposure. Both ferric and ferrous ions could significantly enhance the activity of MAO-B, instead of MAO-A, in SH-SY5Y cells. In addition, iron-induced increase in MAO-B probe fluorescence could be prevented by pargyline and other newly developed MAO-B inhibitors, suggesting that it was MAO-B activity-dependent. These findings may suggest MAO-B is an important sensor in iron-stressed neuronal cells.
Keyphrases
  • induced apoptosis
  • cell cycle arrest
  • iron deficiency
  • endothelial cells
  • small molecule
  • single molecule
  • cell death
  • cell proliferation
  • quantum dots
  • photodynamic therapy
  • fluorescence imaging
  • tandem mass spectrometry