Identification of the amino acid sequence motif of α-synuclein responsible for macrophage activation

被引:48
作者
Lee, Saet-byul [1 ,2 ]
Park, Sang Myun [3 ]
Ahn, Keun Jae [1 ,2 ]
Chung, Kwang Chul [4 ]
Paik, Seung R. [5 ]
Kim, Jongsun [1 ,2 ]
机构
[1] Yonsei Univ, Coll Med, Dept Microbiol, Seoul 120752, South Korea
[2] Yonsei Univ, Coll Med, Inst Immunol & Immunol Dis, Brain Korea Projects Med Sci 21, Seoul 120752, South Korea
[3] Ajou Univ, Sch Med, Dept Pharmacol, Suwon 441749, South Korea
[4] Yonsei Univ, Coll Sci, Dept Biol, Seoul 120749, South Korea
[5] Seoul Natl Univ, Sch Chem & Biol Engn, Coll Engn, Seoul, South Korea
关键词
Synuclein; TNF-alpha; Macrophage; Inflammation; Parkinson's disease; PARKINSONS-DISEASE; HUMAN PLASMA; MUTATION; PROTEIN; AGGREGATION; MICROGLIA; GENE; KINASES; FAMILY; CELLS;
D O I
10.1016/j.bbrc.2009.02.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
alpha-Synuclein (Syn) is implicated in the pathogenesis of PD and related neurodegenerative disorders. Recent studies have also shown that alpha-synuclein can activate microglia and enhance dopaminergic neurodegeneration. The mechanisms of microglia activation by alpha-synuclein, however, are not well understood. In this study, we found that not only alpha-synuclein but also beta- and gamma-synucleins activated macrophages (RAW 264.7) in vitro. Macrophages treated with synuclein proteins secreted TNF-alpha in a dose-dependent manner. Synuclein family proteins also increased mRNA transcription of COX-2 and iNOS. Two alpha-synuclein deletion mutants, Syn Delta NAC and Syn61-140, activated macrophages, while deletion mutants Syn1-60 and Syn96-140 did not significantly activate them. Finally, we demonstrated that macrophage activation by alpha-synuclein was accompanied by phosphorylation of ERK. These results suggest that synuclein family proteins can activate macrophages, and that macrophage activation needs both the N-terminal and C-terminal domains of alpha-synuclein, but not the central NAC region. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:39 / 43
页数:5
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