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PMID: 7699323 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

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

The Journal of experimental medicine ·Vol. 181 ·No. 4 ·1995-04-01 ·Pages 1311-7

Peiper SC, Wang ZX, Neote K, Martin AW, Showell HJ, Conklyn MJ, Ogborne K, Hadley TJ, Lu ZH, Hesselgesser J, Horuk R

Abstract

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.

MeSH Terms
Amino Acid Sequence Antigens, Protozoan Base Sequence Carrier Proteins/biosynthesis,genetics Chemokine CXCL1 Chemokines, CXC Chemotactic Factors/metabolism Duffy Blood-Group System/genetics,metabolism Endocytosis Endothelium, Vascular/metabolism Erythrocyte Membrane/chemistry Gene Expression Genes Genetic Predisposition to Disease Growth Substances/metabolism Humans Intercellular Signaling Peptides and Proteins Interleukin-8/metabolism Malaria, Vivax/genetics Molecular Sequence Data Polymerase Chain Reaction Protozoan Proteins Receptors, Cell Surface/biosynthesis,genetics Recombinant Fusion Proteins/metabolism Transfection Tumor Cells, Cultured Veins
Chemicals
ACKR1 protein, human Antigens, Protozoan CXCL1 protein, human Carrier Proteins Chemokine CXCL1 Chemokines, CXC Chemotactic Factors Duffy Blood-Group System Duffy antigen binding protein, Plasmodium Growth Substances Intercellular Signaling Peptides and Proteins Interleukin-8 Protozoan Proteins Receptors, Cell Surface Recombinant Fusion Proteins
Authors & Affiliations
11 authors, click to expand affiliations / ORCID
Peiper S C
University of Louisville School of Medicine, Kentucky 40292, USA.
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
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Article Info
Journal
The Journal of experimental medicine
Abbr.
J Exp Med
ISSN
0022-1007
Published
1995-04-01
Pages
1311-7
Language
English
Region
United States
NLM ID
2985109R
PMCID
PMC2191961
Subset
IM
Grants
NIDDK NIH HHS · R01-DK43662 · United States
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