Atypical chemokine receptors: from silence to sound

被引:35
作者
Cancellieri, Cinzia [1 ,2 ]
Vacchini, Alessandro [1 ,2 ]
Locati, Massimo [1 ,2 ]
Bonecchi, Raffaella [1 ,2 ]
Borroni, Elena M. [1 ,2 ]
机构
[1] Univ Milan, Dept Med Biotechnol & Translat Med, I-20089 Rozzano, Italy
[2] Humanitas Clin & Res Ctr, I-20089 Rozzano, Italy
关键词
beta-arrestin; atypical chemokine receptor; chemokine; G-protein; PROTEIN-COUPLED RECEPTORS; BETA-ARRESTIN; DECOY RECEPTOR; SIGNAL-TRANSDUCTION; CELL-ADHESION; CXCR7; ACTIVATION; D6; ROLES; C5L2;
D O I
10.1042/BST20120246
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
ACRs (atypical chemokine receptors) were initially referred to as 'silent' receptors on the basis of a lack of signalling and functional activities that are typically observed with conventional chemokine receptors. Although ACRs do not directly induce cell migration, they indirectly control leucocyte recruitment by shaping chemokine gradients in tissues through degradation, transcytosis or local concentration of their cognate ligands. Recent evidence also suggests that these biological activities are supported by G-protein-independent, beta-arrestin-dependent signalling events. In the present article, we review current knowledge on structural and signalling properties of ACRs that are changing our view on this entire class of receptors from silent to endogenous beta-arrestin-biased signalling receptors.
引用
收藏
页码:231 / 236
页数:6
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