DJ-1 protects against dopamine toxicity

被引:85
作者
Lev, Nirit [1 ]
Ickowicz, Debby [1 ]
Barhum, Yael [1 ]
Lev, Shaul [1 ]
Melamed, Eldad [1 ]
Offen, Daniel [1 ]
机构
[1] Tel Aviv Univ, Neurosci Lab, Dept Neurol, Felsenstein Med Res Ctr,Rabin Med Ctr, IL-49100 Petah Tiqwa, Israel
关键词
Dopamine; DJ-1; Parkinson's disease; Oxidative stress; MAP kinases; PARKINSONS-DISEASE; OXIDATIVE STRESS; MOLECULAR PATHWAYS; ALPHA-SYNUCLEIN; CELL-DEATH; MUTATIONS; PARK7; 6-HYDROXYDOPAMINE; NEURODEGENERATION; EXPRESSION;
D O I
10.1007/s00702-008-0134-4
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
Parkinson's disease (PD) is a slowly progressive neurodegenerative disorder characterized by the loss of dopaminergic neurons. Dopamine is a highly toxic compound leading to generation of reactive oxygen species (ROS). DJ-1 mutations lead to early-onset inherited PD. Here, we show that DJ-1 protects against dopamine toxicity. Dopamine-exposure led to upregulation of DJ-1. Overexpression of DJ-1 increased cell resistance to dopamine toxicity and reduced intracellular ROS. Contrary effects were achieved when DJ-1 levels were reduced by siRNA. Similarly, in vivo striatal administration of 6-hydroxydopamine led to upregulation of DJ-1. Upregulation of DJ-1 was mediated by the MAP kinases pathway through activation of ERK 1, 2 in vitro and in vivo. Hence, oxidative stress, generated by free cytoplasmic dopamine, leads to upregulation of DJ-1 through the MAP kinases pathway. This mechanism elucidates how mutations in DJ-1 prompt PD and imply that modulation of DJ-1 may serve as a novel neuroprotective modality.
引用
收藏
页码:151 / 160
页数:10
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