中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Antiasthmatic Drugs Targeting the Cysteinyl Leukotriene Receptor 1 Alleviate Central Nervous System Inflammatory Cell Infiltration and Pathogenesis of Experimental Autoimmune Encephalomyelitis

文献类型:期刊论文

作者Wang, Liefeng1; Du, Changsheng1; Lv, Jie1; Wei, Wei1; Cui, Ye1; Xie, Xin1,2
刊名JOURNAL OF IMMUNOLOGY
出版日期2011-09-01
卷号187期号:5页码:2336-2345
ISSN号0022-1767
DOI10.4049/jimmunol.1100333
文献子类Article
英文摘要Cysteinyl leukotrienes (CysLTs) are potent proinflammatory mediators and are considered to play a key role in inflammatory diseases such as asthma. Antagonists targeting the receptor of CysLTs (CysLT1) are currently used as antiasthmatic drugs. CysLTs have also been implicated in other inflammatory reactions. In this study, we report that in experimental autoimmune encephalomyelitis animals, CysLT1 is upregulated in immune tissue and the spinal cord, and CysLT levels in the blood and cerebrospinal fluid are also higher than in normal mice. Two clinically used antiasthma drugs, montelukast and zafirlukast, both targeting CysLT1, effectively block the CNS infiltration of inflammatory cells and thus reduce the incidence, peak severity, and cumulative clinical scores. Further study indicated that CysLT1 signaling does not affect the differentiation of pathogenic T helper cells. It might affect the pathogenesis of experimental autoimmune encephalomyelitis by increasing the secretion of IL-17 from myelin oligodendrocyte glycoprotein-specific T cells, increasing the permeability of the blood-brain barrier and inducing chemotaxis of T cells. These effects can be blocked by CysLT1 antagonists. Our findings indicate that the antiasthmatic drugs against CysLT1 can also be used to treat multiple sclerosis. The Journal of Immunology, 2011, 187: 2336-2345.
WOS关键词BLOOD-BRAIN-BARRIER ; PROTEIN-COUPLED RECEPTORS ; TIGHT JUNCTION PROTEINS ; MULTIPLE-SCLEROSIS ; VASCULAR-PERMEABILITY ; GENE-EXPRESSION ; MURINE MODEL ; MOUSE MODEL ; MAST-CELLS ; DISEASE
资助项目National Natural Science Foundation of China[31000399] ; National Natural Science Foundation of China[90713047] ; Ministry of Science and Technology of China[2008DFB30150] ; Ministry of Science and Technology of China[2009ZX09302-001] ; Shanghai Commission of Science and Technology[08431910100] ; Shanghai Commission of Science and Technology[09DZ2260100] ; National Basic Research Program of China (973 Program)[2011CB965104] ; Roche RD Center China[00000000]
WOS研究方向Immunology
语种英语
WOS记录号WOS:000294059500038
出版者AMER ASSOC IMMUNOLOGISTS
源URL[http://119.78.100.183/handle/2S10ELR8/278426]  
专题国家新药筛选中心
中科院受体结构与功能重点实验室
新药研究国家重点实验室
通讯作者Xie, Xin
作者单位1.Tongji Univ, Shanghai Key Lab Signaling & Dis Res, Sch Life Sci & Technol, Shanghai 200092, Peoples R China;
2.Chinese Acad Sci, Shanghai Inst Mat Med, Natl Ctr Drug Screening, State Key Lab Drug Res, Shanghai 201203, Peoples R China
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Wang, Liefeng,Du, Changsheng,Lv, Jie,et al. Antiasthmatic Drugs Targeting the Cysteinyl Leukotriene Receptor 1 Alleviate Central Nervous System Inflammatory Cell Infiltration and Pathogenesis of Experimental Autoimmune Encephalomyelitis[J]. JOURNAL OF IMMUNOLOGY,2011,187(5):2336-2345.
APA Wang, Liefeng,Du, Changsheng,Lv, Jie,Wei, Wei,Cui, Ye,&Xie, Xin.(2011).Antiasthmatic Drugs Targeting the Cysteinyl Leukotriene Receptor 1 Alleviate Central Nervous System Inflammatory Cell Infiltration and Pathogenesis of Experimental Autoimmune Encephalomyelitis.JOURNAL OF IMMUNOLOGY,187(5),2336-2345.
MLA Wang, Liefeng,et al."Antiasthmatic Drugs Targeting the Cysteinyl Leukotriene Receptor 1 Alleviate Central Nervous System Inflammatory Cell Infiltration and Pathogenesis of Experimental Autoimmune Encephalomyelitis".JOURNAL OF IMMUNOLOGY 187.5(2011):2336-2345.

入库方式: OAI收割

来源:上海药物研究所

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