CXCR4-CCR5: A couple modulating T cell functions

被引:175
作者
Contento, Rita Lucia [1 ,2 ]
Molon, Barbara [3 ]
Boularan, Cedric [4 ,7 ]
Pozzan, Tullio [1 ,2 ]
Manes, Santos [5 ]
Marullo, Stefano [4 ,7 ]
Viola, Antonella [1 ,6 ]
机构
[1] Venetian Inst Mol Med, I-35129 Padua, Italy
[2] Univ Padua, Dept Biomed Sci, I-35121 Padua, Italy
[3] Ist Ric & Cura Carattere Sci, Ist Oncol Veneto, I-35128 Padua, Italy
[4] Univ Paris 05, Inst Cochin, CNRS, UMR 8104, F-75014 Paris, France
[5] CSIC, Ctr Nacl Biotecnol, Dept Immunol & Oncol, E-28049 Madrid, Spain
[6] Ist Ric & Cura Carattere Sci, Ist Clin Humanitas, I-20089 Milan, Italy
[7] INSERM, U 567, F-75014 Paris, France
关键词
chemokine receptors; heterodimerization; T cell costimulation;
D O I
10.1073/pnas.0804286105
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Chemokines and their receptors direct leukocyte migration among blood, lymph and tissues. Evidence has recently accumulated that, besides their chemotactic functions, chemokine receptors are highly versatile players that fine tune immune responses. During human T cell activation by antigen-presenting cells, the chemokine receptors CCR5 and CXCR4 are recruited into the immunological synapse, where they deliver costimulatory signals. However, the molecular mechanisms allowing signaling versatility of chemokine receptors are unknown. Here, we describe the functional interaction between CXCR4 and CCR5 to exert specific biological functions and modulate T lymphocyte responses. We demonstrate that simultaneous expression and cooperation between CCR5 and CXCR4 are required for chemokine-induced T cell costimulation at the immunological synapse. In addition, we provide evidence for a physical association of the two receptors in a signaling complex that activates distinct T cell functions. We suggest that cooperation between receptors represents one key strategy for the functional plasticity of chemokines.
引用
收藏
页码:10101 / 10106
页数:6
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