Chadzinska M, Golbach L, Pijanowski L, Scheer M, Verburg-van Kemenade B M L
Department of Evolutionary Immunology, Institute of Zoology, Jagiellonian University, Gronostajowa 9, PL30-387 Krakow, Poland.
Cell Biology and Immunology Group, Dept of Animal Sciences, Wageningen University, P.O. Box 338, 6700 AH Wageningen, The Netherlands.
Dev Comp Immunol. 2014 Nov;47(1):68-76. doi: 10.1016/j.dci.2014.07.008. Epub 2014 Jul 15.
Chemokine and chemokine receptor signalling pairs play a crucial role in regulation of cell migration, morphogenesis, and cell activation. Expressed in mammals on activated T and NK cells, chemokine receptor CXCR3 binds interferon-γ inducible chemokines CXCL9-11 and CCL21. Here we sequenced the carp CXCR3 chemokine receptor and showed its relationship to CXCR3a receptors found in other teleosts. We found high expression of the CXCR3 gene in most of the organs and tissues of the immune system and in immune-related tissues such as gills and gut, corroborating a predominantly immune-related function. The very high expression in gill and gut moreover indicates a role for CXCR3 in cell recruitment during infection. High in vivo expression of CXCR3 at later stages of inflammation, as well as its in vitro sensitivity to IFN-γ2 stimulation indicate that in carp, CXCR3 is involved in macrophage-mediated responses. Moreover, as expression of the CXCR3 and CXCb genes coincides in the focus of inflammation and as both the CXCb chemokines and the CXCR3 receptor are significantly up-regulated upon IFN-γ stimulation it is hypothesized that CXCb chemokines may be putative ligands for CXCR3.
趋化因子和趋化因子受体信号对在细胞迁移、形态发生和细胞活化的调节中起着关键作用。趋化因子受体CXCR3在哺乳动物的活化T细胞和NK细胞上表达,它结合干扰素γ诱导的趋化因子CXCL9 - 11和CCL21。在此,我们对鲤鱼CXCR3趋化因子受体进行了测序,并展示了其与其他硬骨鱼中发现的CXCR3a受体的关系。我们发现CXCR3基因在免疫系统的大多数器官和组织以及鳃和肠道等免疫相关组织中高表达,这证实了其主要与免疫相关的功能。此外,CXCR3在鳃和肠道中的极高表达表明其在感染期间细胞募集过程中发挥作用。CXCR3在炎症后期的体内高表达及其在体外对IFN - γ2刺激的敏感性表明,在鲤鱼中CXCR3参与巨噬细胞介导的反应。此外,由于CXCR3和CXCb基因的表达在炎症灶中一致,并且CXCb趋化因子和CXCR3受体在IFN - γ刺激下均显著上调,因此推测CXCb趋化因子可能是CXCR3的假定配体。