Enhanced vulnerability to oxidative stress by α-synuclein mutations and C-terminal truncation

S. Kanda, J. F. Bishop, M. A. Eglitis, Y. Yang, M. M. Mouradian

Research output: Contribution to journalArticlepeer-review

174 Scopus citations


α-Synuclein is a key component of Lewy bodies found in the brains of patients with Parkinson's disease and two point mutations in this protein, Ala53Thr and Ala30Pro, are associated with rare familial forms of the disease. Several lines of evidence suggest the involvement of oxidative stress in the pathogenesis of nigral neuronal death in Parkinson's disease. In the present work we studied the effects of changes in the α-synuclein sequence on the susceptibility of cells to reactive oxygen species. Human dopaminergic neuroblastoma SH-SY5Y cells were stably transduced with various isoforms of α-synuclein and their survival following exposure to hydrogen peroxide or to the dopaminergic neurotoxin MPP+ was assessed. Cells expressing the two point mutant isoforms of α-synuclein were significantly more vulnerable to oxidative stress, with the Ala53Thr engineered cells faring the worst. In addition, cells expressing C-terminally truncated α-synuclein, particularly the 1-120 residue protein, were more susceptible than control β-galactosidase engineered cells.The present experiments indicate that point mutations and C-terminal truncation of α-synuclein exaggerate the susceptibility of dopaminergic cells to oxidative damage. Thus, these observations provide a pathogenetic link between α-synuclein aberrations and a putative cell death mechanism in Parkinson's disease. Copyright (C) 2000 IBRO.

Original languageEnglish (US)
Pages (from-to)279-284
Number of pages6
Issue number2
StatePublished - Apr 2000
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • Neuroscience(all)


  • Cell death
  • Neuron
  • Oxidative stress
  • Parkinson's disease
  • α-Synuclein


Dive into the research topics of 'Enhanced vulnerability to oxidative stress by α-synuclein mutations and C-terminal truncation'. Together they form a unique fingerprint.

Cite this