PEP-1-SOD fusion protein efficiently protects against paraquat-induced dopaminergic neuron damage in a Parkinson disease mouse model

Hee Soon Choi, Jae Jin An, So Young Kim, Sun Hwa Lee, Dae Won Kim, Ki Yeon Yoo, Moo Ho Won, Tae Cheon Kang, Hyung Joo Kwon, Jung Hoon Kang, Sung Woo Cho, Oh Shin Kwon, Jinseu Park, Won Sik Eum, Soo Young Choi

Research output: Contribution to journalArticlepeer-review

76 Scopus citations

Abstract

Parkinson disease (PD) is a common neurodegenerative disorder characterized by the progressive loss of dopaminergic neurons in the substantia nigra (SN). However, the mechanism of the pathology of PD still remains poorly understood. Because the administration of the herbicide paraquat triggers selective dopaminergic neuronal cell death, exposure of mice to this herbicide is one valuable model for studying the pathological aspects of PD. In this study, we investigated the protective effects of PEP-1-SOD in vitro and in vivo under exposure to the herbicide paraquat. The viability of neuronal cells treated with paraquat was markedly increased by transduced PEP-1-SOD. When the PEP-1-SOD fusion protein was injected intraperitoneally into mice, a completely protective effect against dopaminergic neuronal cell death in the SN was observed. This protective effect was synergistically increased when the PEP-1-SOD was cotransduced with Tat-α-synuclein. These results suggest that PEP-1-SOD provides a strategy for therapeutic delivery in various human diseases related to reactive oxygen species, including PD.

Original languageEnglish
Pages (from-to)1058-1068
Number of pages11
JournalFree Radical Biology and Medicine
Volume41
Issue number7
DOIs
StatePublished - 1 Oct 2006

Keywords

  • Dopaminergic neuron
  • Free radicals
  • Oxidative stress
  • Parkinson disease
  • PEP-1-SOD
  • Protein therapy

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