Tanaka Kento, Yoshitomi Tomomi, Hirahara Kazuki
Biologics & Immuno-Oncology Laboratories, Daiichi Sankyo Co., Ltd.
End-Organ Disease Laboratories, Daiichi Sankyo Co., Ltd.
Biol Pharm Bull. 2017;40(5):729-732. doi: 10.1248/bpb.b16-00918.
Chemokine receptors CXCR1 and CXCR2 are conserved between guinea pigs and humans, but the distinct role of each receptor in chemotactic responses of neutrophils against chemokine ligands has not been elucidated due in part to the lack of specific inhibitors against these receptors in guinea pigs. In this study, we investigated the roles of guinea pig CXCR1 and CXCR2 on neutrophils in chemotactic responses to guinea pig interleukin (IL)-8 and growth-regulated oncogene (GRO)α by using specific inhibitory antibodies against these receptors. Neutrophil migration induced by IL-8 was partially inhibited by either anti-CXCR1 antibody or anti-CXCR2 antibody. In addition, the migration was inhibited completely when both anti-CXCR1 and anti-CXCR2 antibodies were combined. On the other hand, neutrophil migration induced by GROα was not inhibited by anti-CXCR1 antibody while inhibited profoundly by anti-CXCR2 antibody. These results indicated that CXCR1 and CXCR2 mediated migration induced by the IL-8 synergistically and only CXCR2 mediated migration induced by GROα in guinea pig neutrophils. Our findings on ligand selectivity of CXCR1 and CXCR2 in guinea pigs are consistent with those in humans.
趋化因子受体CXCR1和CXCR2在豚鼠和人类之间具有保守性,但由于豚鼠缺乏针对这些受体的特异性抑制剂,每种受体在中性粒细胞对趋化因子配体的趋化反应中的独特作用尚未阐明。在本研究中,我们通过使用针对这些受体的特异性抑制抗体,研究了豚鼠CXCR1和CXCR2在中性粒细胞对豚鼠白细胞介素(IL)-8和生长调节致癌基因(GRO)α的趋化反应中的作用。IL-8诱导的中性粒细胞迁移被抗CXCR1抗体或抗CXCR2抗体部分抑制。此外,当抗CXCR1和抗CXCR2抗体联合使用时,迁移被完全抑制。另一方面,GROα诱导的中性粒细胞迁移不受抗CXCR1抗体抑制,而被抗CXCR2抗体显著抑制。这些结果表明,CXCR1和CXCR2协同介导IL-8诱导的迁移,而在豚鼠中性粒细胞中,只有CXCR2介导GROα诱导的迁移。我们关于豚鼠中CXCR1和CXCR2配体选择性的发现与人类中的一致。