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首页> 外文期刊>The Journal of Immunology: Official Journal of the American Association of Immunologists >Stem cell factor plays a major role in the recruitment of eosinophils in allergic pleurisy in mice via the production of leukotriene B4.
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Stem cell factor plays a major role in the recruitment of eosinophils in allergic pleurisy in mice via the production of leukotriene B4.

机译:通过白三烯B4的产生,干细胞因子在小鼠变应性胸膜炎中嗜酸性粒细胞的募集中起主要作用。

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The understanding of the mechanisms underlying eosinophil migration into tissue is an essential step in the development of novel therapies aimed at treating allergic diseases where eosinophil recruitment and activation are thought to play an essential role. In this study, we have examined the effects of the in vivo administration of stem cell factor (SCF) on eosinophil recruitment and tested whether endogenous SCF was involved in mediating eosinophil recruitment in response to Ag challenge in sensitized mice. The intrapleural injection of SCF induced a time- and concentration-dependent recruitment of eosinophils in mice. In allergic mice, SCF message was expressed early after Ag challenge and returned to baseline levels after 8 h. In agreement with the ability of SCF to induce eosinophil recruitment and its expression in the allergic reaction, an anti-SCF polyclonal Ab abrogated eosinophil recruitment when given before Ag challenge. SCF increased the levels of leukotriene B4 (LTB4) in the pleural cavity of mice and an LTB4 receptor antagonist, CP105,696, abrogated the effects of SCF on eosinophil recruitment. Similarly, recruitment of eosinophils in the allergic reaction was virtually abolished by CP105,696. Together, our data favor the hypothesis that the local release of SCF following Ag challenge may activate and/or prime mast cells for IgE-mediated release of inflammatory mediators, especially LTB4. The mediators released in turn drive the recruitment of eosinophils. Inhibition of the function of SCF in vivo may reduce the migration of eosinophils to sites of allergic inflammation and may, thus, be a relevant principle in the treatment of allergic diseases.
机译:理解嗜酸性粒细胞迁移进入组织的机制是开发旨在治疗变应性疾病的新方法的必不可少的步骤,其中认为嗜酸性粒细胞的募集和激活起着至关重要的作用。在这项研究中,我们检查了体内施用干细胞因子(SCF)对嗜酸性粒细胞募集的影响,并测试了内源性SCF是否参与介导嗜酸性粒细胞募集以应对敏感小鼠的Ag攻击。胸膜内注射SCF诱导小鼠嗜酸性粒细胞的时间和浓度依赖性募集。在变态反应小鼠中,Ag攻击后早期就表达了SCF信息,并在8小时后恢复到基线水平。与SCF诱导嗜酸性粒细胞募集及其在变态反应中的表达相一致,抗-SCF多克隆Ab在Ag攻击前给予可废除嗜酸性粒细胞募集。 SCF增加了小鼠胸膜腔中白三烯B4(LTB4)的水平,LTB4受体拮抗剂CP105,696废除了SCF对嗜酸性粒细胞募集的影响。同样,CP105,696实质上消除了过敏反应中嗜酸性粒细胞的募集。总之,我们的数据支持这样一个假说,即Ag攻击后SCF的局部释放可能激活和/或引发肥大细胞,用于IgE介导的炎症介质(尤其是LTB4)的释放。释放的介体又推动了嗜酸性粒细胞的募集。在体内抑制SCF的功能可以减少嗜酸性粒细胞向变应性炎症部位的迁移,因此可能是治疗变应性疾病的相关原理。

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