Similarities and differences in RANTES- and (AOP)-RANTES-triggered signals:: Implications for chemotaxis

被引:105
作者
Rodríguez-Frade, JM
Vila-Coro, AJ
Martín, A
Nieto, M
Sánchez-Madrid, F
Proudfoot, AEI
Wells, TNC
Martínez, C
Mellado, M
机构
[1] Univ Autonoma Madrid, CSIC, Ctr Nacl Biotecnol, Dept Immunol & Oncol, E-28049 Madrid, Spain
[2] Univ Autonoma Madrid, Hosp Princesa, Serv Inmunol, E-28006 Madrid, Spain
[3] Serono Pharmaceut Res Inst, CH-1228 Geneva, Switzerland
关键词
chemokines; receptor dimerization; inflammation; HIV-1;
D O I
10.1083/jcb.144.4.755
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Chemokines are a family of proinflammatory cytokines that attract and activate specific types of leukocytes. Chemokines mediate their effects via interaction with seven transmembrane G protein-coupled receptors (GPCR). Using CCR5-transfected HEK-293 cells, we show that both the CCR5 ligand, RANTES, as well as its derivative, aminooxypentane (AOP)-RANTES, trigger immediate responses such as Ca2+ influx, receptor dimerization, tyrosine phosphorylation, and G alpha(i) as well as JAK/STAT association to the receptor. In contrast to RANTES, (AOP)-RANTES is unable to trigger late responses, as measured by the association of focal adhesion kinase (FAK) to the chemokine receptor complex, impaired cell polarization required for migration, or chemotaxis. The results are discussed in the context of the dissociation of the late signals, provoked by the chemokines required for cell migration, from early signals.
引用
收藏
页码:755 / 765
页数:11
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