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Chemokines Cytokines and Interleukins: The coordinated action of G-CSF and ELR + CXC chemokines in neutrophil mobilization during acute inflammation

机译:趋化因子细胞因子和白介素:G-CSF和ELR + CXC趋化因子在急性炎症期间中性粒细胞动员中的协同作用

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摘要

In this study, we have identified a unique combinatorial effect of the chemokines KC/MIP-2 and the cytokine granulocyte colony-stimulating factor (G-CSF) with respect to the rapid mobilization of neutrophils from the bone marrow in a model of acute peritonitis. At 2 hours following an intraperitoneal injection of thioglycollate, there was a 4.5-fold increase in blood neutrophil numbers, which was inhibited 84% and 72% by prior administration of blocking mAbs against either the chemokines KC/MIP-2 or G-CSF, respectively. An intraperitoneal injection of G-CSF acted remotely to stimulate neutrophil mobilization, but did not elicit recruitment into the peritoneum. Further, in vitro G-CSF was neither chemotactic nor chemokinetic for murine neutrophils, and had no priming effect on chemotaxis stimulated by chemokines. Here, we show that, in vitro and in vivo, G-CSF induces neutrophil mobilization by disrupting their SDF-1α–mediated retention in the bone marrow. Using an in situ perfusion system of the mouse femoral bone marrow to directly assess mobilization, KC and G-CSF mobilized 6.8 × 106 and 5.4 × 106 neutrophils, respectively, while the infusion of KC and G-CSF together mobilized 19.5 × 106 neutrophils, indicating that these factors act cooperatively with respect to neutrophil mobilization.
机译:在这项研究中,我们已经确定了趋化因子KC / MIP-2和细胞因子粒细胞集落刺激因子(G-CSF)在急性腹膜炎模型中从骨髓快速动员中性粒细胞方面具有独特的组合作用。腹腔内注射巯基乙酸盐后2小时,血液中性粒细胞数量增加了4.5倍,事先给予针对趋化因子KC / MIP-2或G-CSF的封闭mAb抑制了84%和72%,分别。腹膜内注射G-CSF可以远程刺激中性粒细胞的动员,但并未引起其募集进入腹膜。此外,体外G-CSF对鼠中性粒细胞既没有趋化性也没有化学动力学,对趋化因子刺激的趋化性没有引发作用。在这里,我们表明,在体外和体内,G-CSF都通过破坏SDF-1α介导的在骨髓中的滞留而诱导中性粒细胞动员。使用小鼠股骨原位灌注系统直接评估动员,KC和G-CSF分别动员了6.8×10 6 和5.4×10 6 中性粒细胞。而KC和G-CSF的输注一起动员了19.5×10 6 中性粒细胞,表明这些因素在中性粒细胞动员方面起协同作用。

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