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CXCR7、CXCR4与CXCL12:一个奇特的组合?

CXCR7, CXCR4 and CXCL12: an eccentric trio?

作者信息

Thelen Marcus, Thelen Sylvia

机构信息

Institute for Research in Biomedicine, CH-6500 Bellinzona, Switzerland.

出版信息

J Neuroimmunol. 2008 Jul 31;198(1-2):9-13. doi: 10.1016/j.jneuroim.2008.04.020. Epub 2008 Jun 3.

Abstract

CXCR7, formerly called RDC1 is a recently deorphanized G-protein coupled receptor which binds with high affinity the inflammatory and homing chemokines CXCL11/ITAC and CXCL12/SDF-1. Despite its phylogenetic relation and ligand binding properties CXCR7 does not mediate typical chemokine receptor responses such as leukocyte trafficking. Recent findings in zebrafish indicate that a critical activity of the receptor is scavenging of CXCL12 thereby generating guidance cues for CXCR4-dependent migration. The observations do not exclude the possibility that the receptor is capable of inducing signal transduction which is suggestive from studies of tumor growth and survival. The pronounced expression in central and peripheral nervous tissue and the absence of a brain phenotype in CXCR7(-/-) mice suggest a subtle activity of the receptor.

摘要

CXCR7,以前称为RDC1,是一种最近才明确其功能的G蛋白偶联受体,它能与炎症趋化因子和归巢趋化因子CXCL11/ITAC以及CXCL12/SDF-1高亲和力结合。尽管CXCR7在系统发育关系和配体结合特性方面有一定特点,但它并不介导典型的趋化因子受体反应,如白细胞迁移。斑马鱼的最新研究结果表明,该受体的一个关键活性是清除CXCL12,从而为依赖CXCR4的迁移产生引导信号。这些观察结果并不排除该受体能够诱导信号转导的可能性,肿瘤生长和存活研究也暗示了这一点。CXCR7在中枢和外周神经组织中的显著表达以及CXCR7基因敲除小鼠中无脑部表型,提示该受体具有微妙的活性。

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