Alpha-synuclein overexpression increases dopamine toxicity in BE2-M17 cells

BMC Neurosci. 2010 Mar 25:11:41. doi: 10.1186/1471-2202-11-41.

Abstract

Background: Oxidative stress has been proposed to be involved in the pathogenesis of Parkinson's disease (PD). A plausible source of oxidative stress in nigral dopaminergic neurons is the redox reactions that specifically involve dopamine and produce various toxic molecules, i.e., free radicals and quinone species. alpha-Synuclein, a protein found in Lewy bodies characteristic of PD, is also thought to be involved in the pathogenesis of PD and point mutations and multiplications in the gene coding for alpha-synuclein have been found in familial forms of PD.

Results: We used dopaminergic human neuroblastoma BE(2)-M17 cell lines stably transfected with WT or A30P mutant alpha-synuclein to characterize the effect of alpha-synuclein on dopamine toxicity. Cellular toxicity was analyzed by lactate dehydrogenase assay and by fluorescence-activated cell sorter analysis. Increased expression of either wild-type or mutant alpha-synuclein enhances the cellular toxicity induced by the accumulation of intracellular dopamine or DOPA.

Conclusions: Our results suggest that an interplay between dopamine and alpha-synuclein can cause cell death in a neuron-like background. The data presented here are compatible with several models of cytotoxicity, including the formation of alpha-synuclein oligomers and impairment of the lysosomal degradation.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, N.I.H., Intramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis / physiology
  • Cell Death / physiology
  • Cell Line, Tumor
  • Cell Survival / physiology
  • Dihydroxyphenylalanine / metabolism
  • Dopamine / metabolism*
  • Fluorescence
  • Humans
  • L-Lactate Dehydrogenase / metabolism
  • Mutation, Missense
  • Necrosis / metabolism
  • Neuroblastoma / metabolism*
  • Neurons / metabolism
  • Parkinson Disease
  • Transfection
  • alpha-Synuclein / genetics
  • alpha-Synuclein / metabolism*

Substances

  • alpha-Synuclein
  • Dihydroxyphenylalanine
  • L-Lactate Dehydrogenase
  • Dopamine