Peiper S C, Wang Z X, Neote K, Martin A W, Showell H J, Conklyn M J, Ogborne K, Hadley T J, Lu Z H, Hesselgesser J, Horuk R
University of Louisville School of Medicine, Kentucky 40292, USA.
J Exp Med. 1995 Apr 1;181(4):1311-7. doi: 10.1084/jem.181.4.1311.
The Duffy antigen/receptor for chemokines (DARC), first identified on erythrocytes, functions not only as a promiscuous chemokine receptor but also as a receptor for the malarial parasite, Plasmodium vivax. The recent finding that DARC is ubiquitously expressed by endothelial cells lining postcapillary venules provides a possible insight into the function of this receptor because this anatomic site is an active interface for leukocyte trafficking. However, the biological significance of DARC is questionable since it has not yet been determined whether individuals lacking the expression of this protein on their erythrocytes (Duffy negative individuals), who are apparently immunologically normal, express the receptor on endothelial cells. However, we report here that DARC is indeed expressed in endothelial cells lining postcapillary venules and splenic sinusoids in individuals who lack the erythrocyte receptor. These findings are based on immunohistochemical, biochemical, and molecular biological analysis of tissues from Duffy negative individuals. We also present data showing that, in contrast to erythrocyte DARC, cells transfected with DARC internalize radiolabeled ligand. We conclude that the DARC may play a critical role in mediating the effects of proinflammatory chemokines on the interactions between leukocyte and endothelial cells since the molecular pathology of the Duffy negative genotype maintains expression on the latter cell type.
趋化因子的达菲抗原/受体(DARC)最初是在红细胞上发现的,它不仅作为一种通用的趋化因子受体发挥作用,还作为间日疟原虫这种疟原虫的受体。最近发现,毛细血管后微静脉的内皮细胞普遍表达DARC,这为了解该受体的功能提供了一个可能的切入点,因为这个解剖部位是白细胞运输的活跃界面。然而,DARC的生物学意义存在疑问,因为尚未确定红细胞上缺乏该蛋白表达的个体(达菲阴性个体),尽管他们显然免疫功能正常,其内皮细胞上是否表达该受体。然而,我们在此报告,在缺乏红细胞受体的个体中,DARC确实在毛细血管后微静脉和脾血窦的内皮细胞中表达。这些发现基于对达菲阴性个体组织的免疫组织化学、生物化学和分子生物学分析。我们还展示了数据,表明与红细胞DARC不同,转染了DARC的细胞会内化放射性标记的配体。我们得出结论,DARC可能在介导促炎趋化因子对白细胞与内皮细胞之间相互作用的影响中起关键作用,因为达菲阴性基因型的分子病理学在后者细胞类型上维持了表达。