中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
A novel molecular mechanism for nitrated alpha-synuclein-induced cell death

文献类型:期刊论文

作者Liu, Yanying1; Qiang, Min1; Wei, Yan1; He, Rongqiao1,2
刊名JOURNAL OF MOLECULAR CELL BIOLOGY
出版日期2011-08-01
卷号3期号:4页码:239-249
关键词nitric oxide nitration neuronal death toxicity focal adhesion kinase calcium-independent inducible nitric oxide synthase
ISSN号1674-2788
产权排序2
通讯作者He, RQ (reprint author), Chinese Acad Sci, Inst Biophys, State Key Lab Brain & Cognit Sci, 15 Datun Rd, Beijing 100101, Peoples R China.
英文摘要Although previous studies have demonstrated the involvement of nitrated alpha-synuclein in neurodegenerative disorders (synucleinopathies), the effects of nitrated alpha-synuclein and the molecular mechanisms underlying its toxicity are still unclear. In the present study, nitrated alpha-synuclein with four 3-nitrotyrosines (Tyr(39), Tyr(125), Tyr(133), and Tyr(136)) was obtained non-enzymatically by incubation with nitrite. The nitrated protein existed as a mixture of monomers, dimers, and polymers in solution. The nitrated alpha-synuclein could induce cell death in a time-and concentration-dependent manner when SH-SY5Y cells (a human neuroblastoma cell line) were incubated with the dimers and polymers. Treatment with anti-integrin alpha 5 beta 1 antibody partially rescued the SH-SY5Y cells from the cell death. Dot blotting and immunoprecipitation revealed that the nitrated protein bound to integrin on the cell membranes. Level of nitric oxide (NO) and calcium-independent inducible NO synthase (iNOS) activity increased during the initial stages of the treatment. The expression of phosphorylated focal adhesion kinase (FAK) decreased in the cells. Subsequently, an increase in caspase 3 activity was observed in SH-SY5Y cells. Our results demonstrate that activation of iNOS and inhibition of FAK may both be responsible for the cell death induced by nitrated alpha-synuclein. These data suggest that the cytotoxicity of nitrated alpha-synuclein is mediated via an integrin-iNOS/-FAK signaling pathway, and that the nitration of alpha-synuclein plays a role in neuronal degeneration.
学科主题Physiological psychology/Biological Psychology
收录类别SCI
项目简介This work was supported by the grants from the China Postdoctoral Science Foundation (20070410153, 200801120), the National Science Foundation of China (30970695), the Major State Basic Research Development Program of China (973 Program) (2010CB912303), and the Chinese Academy of Sciences (KSCX2-YW-R-119, KSCX2-YW-R-256).
原文出处http://jmcb.oxfordjournals.org/content/3/4/239.full.pdf+html
语种英语
WOS记录号WOS:000293624000006
源URL[http://ir.psych.ac.cn/handle/311026/10852]  
专题心理研究所_脑与认知科学国家重点实验室
作者单位1.Chinese Acad Sci, Inst Biophys, State Key Lab Brain & Cognit Sci, Beijing 100101, Peoples R China
2.Chinese Acad Sci, Inst Psychol, Key Lab Mental Hlth, Beijing 100101, Peoples R China
推荐引用方式
GB/T 7714
Liu, Yanying,Qiang, Min,Wei, Yan,et al. A novel molecular mechanism for nitrated alpha-synuclein-induced cell death[J]. JOURNAL OF MOLECULAR CELL BIOLOGY,2011,3(4):239-249.
APA Liu, Yanying,Qiang, Min,Wei, Yan,&He, Rongqiao.(2011).A novel molecular mechanism for nitrated alpha-synuclein-induced cell death.JOURNAL OF MOLECULAR CELL BIOLOGY,3(4),239-249.
MLA Liu, Yanying,et al."A novel molecular mechanism for nitrated alpha-synuclein-induced cell death".JOURNAL OF MOLECULAR CELL BIOLOGY 3.4(2011):239-249.

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来源:心理研究所

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