α-synuclein induces apoptosis by altered expression in human peripheral lymphocytes in Parkinson's disease

被引:69
作者
Kim, S
Jeon, BS
Heo, C
Im, PS
Ahn, TB
Seo, JH
Kim, HS
Park, CH
Choi, SH
Cho, SH
Lee, WJ
Suh, YH [1 ]
机构
[1] Seoul Natl Univ, Coll Med, Dept Pharmacol,MRC, Natl Creat Res Initiat Ctr Alzheimers Dementia &, Seoul 110799, South Korea
[2] Seoul Natl Univ, Coll Med, Dept Neurol, Clin Res Inst, Seoul 10799, South Korea
[3] Seoul Natl Univ Hosp, MRC, Seoul 10799, South Korea
[4] Kyung Hee Univ Hosp, Dept Neurol, Seoul 130702, South Korea
[5] Seoul Natl Univ, Coll Med, Dept Anat, Seoul 110799, South Korea
关键词
glucocorticoid receptor; reactive oxygen species; GC;
D O I
10.1096/fj.04-1917fje
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Though the etiology of Parkinson's disease (PD) remains unclear, alpha-synuclein (alpha-SN) is regarded as a major causative agent of PD. Several lines of evidence indicate that immunological abnormalities are associated with PD for unknown reasons. The present study was performed to assess whether peripheral blood mononuclear cells (PBMCs) show altered alpha-SN expression in PD patients and to identify its functions, which may be related to peripheral immune abnormalities in PD. alpha-SN was found to be expressed more in 151 idiopathic PD (IPD) patients than in 101 healthy controls, who nevertheless showed as age-dependent increases. By in vitro transfection, alpha-SN expression was shown to be correlated with glucocorticoid sensitive apoptosis, possibly caused by the enhanced expression of glucocorticoid receptor (GR), caspase activations (caspase-8, caspase-9), CD95 up-regulation, and reactive oxygen species (ROS) production. An understanding of the correlation between alpha-SN levels and apoptosis in the presence of the coordinated involvement of multiple processes would provide an insight into the molecular basis of the disease. The present study provides a clue that the alpha-SN may be one of the primary causes of the immune abnormalities observed in PD and offers new targets for pharmacotherapeutic intervention.
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收藏
页码:1615 / +
页数:21
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