Elsner J, Dulkys Y, Kimmig D, Wells T N, Proudfoot A E, Kapp A
Department of Dermatology and Allergology, Hannover Medical University, Hannover, Germany.
Int Arch Allergy Immunol. 2001 Jan-Mar;124(1-3):227-9. doi: 10.1159/000053719.
Eosinophils are predominant effector cells in allergic diseases attracted by several CC chemokines into the inflammatory tissue. According to their important role in attracting leukocytes, several kinds of chemokine receptor antagonists have been developed. Therefore, the aim of this study was to investigate the effect of aminooxypentane (AOP)-RANTES on the activation of the CC chemokine receptor 3, CCR3, exemplary on human eosinophils, because they represent the dominant CCR3+ cell type. AOP-RANTES dose-dependently induced an increase of intracellular calcium concentration (Ca(2+)) and a release of reactive oxygen species, which could be inhibited by pertussis toxin, in human eosinophils from normal nonatopic donors. AOP-RANTES was as effective as RANTES but less effective than eotaxin and eotaxin-2 in the activation of the respiratory burst. Flow-cytometric analyses revealed that eosinophils constitutively expressed the CC chemokine receptors CCR1 and CCR3, whereas CCR5 was not expressed. AOP-RANTES, RANTES, eotaxin and eotaxin-2, but not Met-RANTES, induced a downregulation of CCR3 at 37 degrees C. Reexpression of CCR3 on eosinophils was observed within 120 min. Whereas no differences of CCR3 downregulation and recycling after stimulation with AOP-RANTES, RANTES, eotaxin and eotaxin-2 were found there exists a distinct profile of activity with respect to the activation of the respiratory burst in human eosinophils.
嗜酸性粒细胞是过敏性疾病中的主要效应细胞,被多种CC趋化因子吸引至炎症组织。鉴于其在吸引白细胞方面的重要作用,已开发出多种趋化因子受体拮抗剂。因此,本研究旨在探讨氨氧基戊烷(AOP)-RANTES对CC趋化因子受体3(CCR3)激活的影响,以人嗜酸性粒细胞为例,因为它们是主要的CCR3+细胞类型。AOP-RANTES可剂量依赖性地诱导正常非特应性供体的人嗜酸性粒细胞内细胞钙浓度(Ca(2+))升高和活性氧释放,这可被百日咳毒素抑制。在呼吸爆发的激活方面,AOP-RANTES与RANTES效果相当,但不如嗜酸性粒细胞趋化因子和嗜酸性粒细胞趋化因子-2有效。流式细胞术分析显示,嗜酸性粒细胞组成性表达CC趋化因子受体CCR1和CCR3,而不表达CCR5。AOP-RANTES、RANTES、嗜酸性粒细胞趋化因子和嗜酸性粒细胞趋化因子-2(而非甲硫氨酸-RANTES)在37℃时可诱导CCR3下调。在120分钟内可观察到嗜酸性粒细胞上CCR3的重新表达。虽然在用AOP-RANTES、RANTES、嗜酸性粒细胞趋化因子和嗜酸性粒细胞趋化因子-2刺激后,CCR3下调和再循环没有差异,但在人嗜酸性粒细胞呼吸爆发的激活方面存在明显的活性特征。