Chemokine receptor dimerization:: two are better than one

被引:92
作者
Rodríguez-Frade, JM [1 ]
Mellado, M [1 ]
Martínez, C [1 ]
机构
[1] Univ Autonoma Madrid, CSIC, Ctr Nacl Biotecnol, Dept Immunol & Oncol, E-28049 Madrid, Spain
关键词
D O I
10.1016/S1471-4906(01)02036-1
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The chemokines participate in an exceptional range of physiological and pathological processes, including the control of lymphocyte trafficking, tumor growth, wound healing, allograft rejection, regulation of T-cell differentiation, asthma, infection with HIV and atherosclerosis. This vast array of activities is triggered by the interaction of nearly 50 different chemokines with a relatively modest number of 20 G-protein-coupled receptors. The asymmetry between the number of receptors and ligands suggests an underlying, shared control mechanism activated at a very early stage of the response. One of the first events triggered by the binding of chemokines is the homo- and heterodimerization of their receptors; here, we outline these events and their consequences in chemokine signaling.
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页码:612 / 617
页数:6
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