CHEMOATTRACTANT RECEPTORS FOR INTERLEUKIN-8 AND C5A - EXPRESSION ON PERIPHERAL-BLOOD LEUKOCYTES AND DIFFERENTIAL REGULATION ON HL-60 AND AML-193 CELLS BY VITAMIN-D-3 AND ALL-TRANS-RETINOIC ACID
S. Zahn et al., CHEMOATTRACTANT RECEPTORS FOR INTERLEUKIN-8 AND C5A - EXPRESSION ON PERIPHERAL-BLOOD LEUKOCYTES AND DIFFERENTIAL REGULATION ON HL-60 AND AML-193 CELLS BY VITAMIN-D-3 AND ALL-TRANS-RETINOIC ACID, European Journal of Immunology, 27(4), 1997, pp. 935-940
Two homologous high-affinity receptors for the chemoattractant interle
ukin-8, IL-8RA and IL-8RB, and one for the chemoattractant C5a (C5aR)
have been cloned. These membrane proteins are members of the rhodopsin
superfamily of G-protein coupled seven-transmembrane segment receptor
s. New monoclonal antibodies (mAb) directed against the deduced N-term
inal sequences of the IL-8RA (mAb SE2) and IL-8RB (mAb HC2) were gener
ated to determine the IL-8R expression on human blood leukocytes and t
wo human myeloid cell lines. The C5aR expression was detected using th
e mAb W17/1. Approximately 107 000 C5aR, 55 000 IL-8RA, and 25 000 IL-
8RB molecules per cell could be detected on human granulocytes by flow
cytometric analysis. On peripheral blood monocytes, 42 000 C5aR molec
ules/cell and 3000 IL-8RB molecules/cell were expressed. However, we w
ere unable to quantitate IL-8RA expression, which was detectable but b
elow 2500 molecules per cell and thus outside the standard range for t
he quantitation of receptor molecules by flow cytometry. On AML-193 ce
lls, only the IL-8RB was constitutively expressed, whereas on HL-60 ce
lls, we could not detect expression of any of the three receptors. Vit
amin D-3 (250 ng/ml, 7 days), which has been shown to induce different
iation of AML-193 and HL-60 cells into the monocytic phenotype, led to
an upregulation of IL-8RB and C5aR in both cell lines in the absence
of any expression of IL-8RA. In contrast, all-trans retinoic acid (0.1
mu M, 7 days), which induces differentiation into the granulocytic ph
enotype, led to an up-regulation of IL-8RB in AML-193 cells and to an
expression of IL-8RB and C5aR in HL-60 cells. Again, neither cell line
expressed IL-8RA. These findings suggest that regulation of IL-8RA ex
pression differs from that of its IL-8RB homolog and may be a late eve
nt in leukocyte maturation.