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Chemokines Cytokines and Interleukins: Scavenging roles of chemokine receptors: chemokine receptor deficiency is associated with increased levels of ligand in circulation and tissues

机译:趋化因子细胞因子和白介素:趋化因子受体的清除作用:趋化因子受体的缺乏与循环和组织中配体水平的升高有关

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摘要

In vitro studies have implicated chemokine receptors in consumption and clearance of specific ligands. We studied the role that various signaling chemokine receptors play during ligand homeostasis in vivo. We examined the levels of ligands in serum and CNS tissue in mice lacking chemokine receptors. Compared with receptor-sufficient controls, Cx3cr1−/− mice exhibited augmented levels of CX3CL1 both in serum and brain, and circulating levels of CXCL1 and CXCL2 were increased in Cxcr2−/− mice. CCR2-deficient mice showed significantly increased amounts of circulating CCL2 compared with wild-type mice. Cxcr3−/− mice revealed increased levels of circulating and brain CXCL10 after experimental autoimmune encephalomyelitis (EAE) induction. CCR2-deficient peripheral blood and resident peritoneal cells exhibited reduced binding capacity and biologic responses to the CCR1 ligand CCL3, suggesting that elevated levels of CCR2 ligands had down-regulated CCR1. The results indicate that signaling chemokine receptors clear chemokines from circulation and tissues. These homeostatic functions of signaling chemokine receptors need to be integrated into safety and efficacy calculations when considering therapeutic receptor blockade.
机译:体外研究表明趋化因子受体与特定配体的消耗和清除有关。我们研究了体内各种配体稳态过程中各种信号趋化因子受体的作用。我们检查了缺乏趋化因子受体的小鼠血清和中枢神经系统组织中的配体水平。与受体充足的对照组相比,Cx3cr1 -/-小鼠的血清和脑中CX3CL1的水平均升高,而Cxcr2 -/-老鼠。与野生型小鼠相比,缺乏CCR2的小鼠显示循环CCL2的量显着增加。 Cxcr3 -/-小鼠在实验性自身免疫性脑脊髓炎(EAE)诱导后显示循环和脑CXCL10水平升高。缺乏CCR2的外周血和常驻腹膜细胞对CCR1配体CCL3的结合能力和生物学反应降低,这表明CCR2配体水平的升高下调了CCR1。结果表明,信号趋化因子受体清除了循环和组织中的趋化因子。考虑治疗性受体阻滞时,需要将信号趋化因子受体的这些稳态功能整合到安全性和功效计算中。

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