G protein-coupled receptors as therapeutic targets for multiple sclerosis

被引:41
|
作者
Du, Changsheng [1 ]
Xie, Xin [1 ,2 ]
机构
[1] Tongji Univ, Lab Receptor Based BioMed, Shanghai Key Lab Signaling & Dis Res, Sch Life Sci & Technol, Shanghai 200092, Peoples R China
[2] Chinese Acad Sci, State Key Lab Drug Res, Natl Ctr Drug Screening, Shanghai Inst Mat Med, Shanghai 201203, Peoples R China
基金
中国国家自然科学基金;
关键词
G protein-coupled receptors (GPCRs); multiple sclerosis (MS); experimental autoimmune encephalomyelitis (EAE); agonist; antagonist; therapeutic targets; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; CENTRAL-NERVOUS-SYSTEM; EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS; BLOOD MONONUCLEAR-CELLS; MACROPHAGE INFLAMMATORY PROTEIN-1-ALPHA; BETA-ENDORPHIN CONCENTRATIONS; IMMUNOMODULATORY DRUG FTY720; LYMPHOID CHEMOKINES CCL19; CLINICAL-DISEASE ACTIVITY; IA ANTIGEN-EXPRESSION;
D O I
10.1038/cr.2012.87
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
G protein-coupled receptors (GPCRs) mediate most of our physiological responses to hormones, neurotransmitters and environmental stimulants. They are considered as the most successful therapeutic targets for a broad spectrum of diseases. Multiple sclerosis (MS) is an inflammatory disease that is characterized by immune-mediated demyelination and degeneration of the central nervous system (CNS). It is the leading cause of non-traumatic disability in young adults. Great progress has been made over the past few decades in understanding the pathogenesis of MS. Numerous data from animal and clinical studies indicate that many GPCRs are critically involved in various aspects of MS pathogenesis, including antigen presentation, cytokine production, T-cell differentiation, T-cell proliferation, T-cell invasion, etc. In this review, we summarize the recent findings regarding the expression or functional changes of GPCRs in MS patients or animal models, and the influences of GPCRs on disease severity upon genetic or pharmacological manipulations. Hopefully some of these findings will lead to the development of novel therapies for MS in the near future.
引用
收藏
页码:1108 / 1128
页数:21
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