Contento Rita Lucia, Molon Barbara, Boularan Cedric, Pozzan Tullio, Manes Santos, Marullo Stefano, Viola Antonella
Venetian Institute of Molecular Medicine, via Orus 2, 35129 Padua, Italy.
Proc Natl Acad Sci U S A. 2008 Jul 22;105(29):10101-6. doi: 10.1073/pnas.0804286105. Epub 2008 Jul 15.
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.
趋化因子及其受体引导白细胞在血液、淋巴和组织之间迁移。最近有越来越多的证据表明,除了其趋化功能外,趋化因子受体是调节免疫反应的高度多功能参与者。在抗原呈递细胞激活人类T细胞的过程中,趋化因子受体CCR5和CXCR4被招募到免疫突触中,在那里它们传递共刺激信号。然而,趋化因子受体实现信号传导多功能性的分子机制尚不清楚。在这里,我们描述了CXCR4和CCR5之间的功能相互作用,以发挥特定的生物学功能并调节T淋巴细胞反应。我们证明,CCR5和CXCR4的同时表达与合作是趋化因子在免疫突触处诱导T细胞共刺激所必需的。此外,我们提供了证据表明这两种受体在激活不同T细胞功能的信号复合物中存在物理关联。我们认为受体之间的合作是趋化因子功能可塑性的一种关键策略。