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Differential expression of the Duffy antigen receptor for chemokines according to RBC age and FY genotype
Author(s) -
Woolley I.J.,
Hotmire K.A.,
Sramkoski R.M.,
Zimmerman P.A.,
Kazura J.W.
Publication year - 2000
Publication title -
transfusion
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.045
H-Index - 132
eISSN - 1537-2995
pISSN - 0041-1132
DOI - 10.1046/j.1537-2995.2000.40080949.x
Subject(s) - biology , context (archaeology) , genotype , plasmodium vivax , immunology , flow cytometry , chemokine , antigen , chemokine receptor , cc chemokine receptors , microbiology and biotechnology , proinflammatory cytokine , virology , immune system , malaria , gene , genetics , plasmodium falciparum , inflammation , paleontology
BACKGROUND: The Duffy (Fy) blood group (also known as Duffy antigen receptor for chemokines, or DARC ) may be involved in regulation of the level of circulating proinflammatory chemokines, and it is an obligatory receptor on RBCs for the human malaria parasite Plasmodium vivax . STUDY DESIGN AND METHODS: Because quantification of Fy expression by using RBCs of various ages will not detect acute changes associated with inflammatory states, and because P. vivax exclusively invades reticulocytes, a flow cytometric method was developed to measure the level of surface expression of Fy. Reticulocytes and mature RBCs from persons with different genotypes (GATA‐1 T→C promoter mutation at nt –46; FY*A and FY*B in the ORF) were used. RESULTS: Expression of the Fy6 epitope, which is required for P. vivax invasion, was 49 ± 19 percent higher on reticulocytes than on mature RBCs, regardless of donor genotype (p<0.0001). Fy6 levels were approximately 50 percent lower in persons who were heterozygous for the GATA‐1 promoter mutation and were significantly lower on reticulocytes and mature RBCs of the FY*B / FY*B genotype than on those of the FY*A / FY*A or FY*A / FY*B genotype. CONCLUSION: Fy has greater expression on reticulocytes than on mature RBCs in flow cytometry. This method may be useful in further studies of this antigen, such as characterization of reticulocytes and RBC phenotypes across populations, in response to chemokine regulation, and in the context of susceptibility to P. vivax and other parasites.