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The Duffy antigen/receptor for chemokines (DARC) is expressed in endothelial cells of Duffy negative individuals who lack the erythrocyte receptor

机译:Duffy抗原/趋化因子受体(DARC)在缺乏红细胞受体的Duffy阴性个体的内皮细胞中表达

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摘要

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.
机译:达菲(Duffy)趋化因子抗原/受体(DARC),首先在红细胞上被发现,不仅起混杂的趋化因子受体的作用,而且还作为疟原虫间日疟原虫的受体。最近的发现表明DARC由毛细血管后小静脉内衬的内皮细胞广泛表达,为这种受体的功能提供了可能的见解,因为该解剖部位是白细胞运输的活跃界面。然而,DARC的生物学意义是有疑问的,因为尚未确定在免疫学上是否正常的红细胞上缺乏该蛋白表达的个体(达菲阴性个体)是否在内皮细胞上表达受体。但是,我们在这里报告说,在缺乏红细胞受体的个体中,DARC确实在毛细血管后小静脉和脾窦内衬的内皮细胞中表达。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。我们还提供的数据表明,与红细胞DARC相比,用DARC转染的细胞可将放射性标记的配体内化。我们得出结论,由于达菲阴性基因型的分子病理学在后一种细胞类型上保持表达,因此DARC可能在介导促炎性趋化因子对白细胞与内皮细胞之间的相互作用中起关键作用。

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