The C5a receptor belongs to the superfamily of G-protein coupled recep
tors with seven transmembrane segments. In this study we report on the
cloning of the rat C5a receptor (ratC5aR). We used a hybridization pr
obe produced by PCR utilizing degenerate primers which corresponded to
conserved parts of the human, canine and murine C5a receptor nucleoti
de sequences and to the published partial amino acid sequence of the r
at C5a receptor to screen a rat macrophage cDNA library. We found two
overlapping clones containing an open reading frame of 1056 bp, a 3' u
ntranslated region of 683 bp and a 5' untranslated region of 27 bp. Th
e overall nucleotide acid sequence identity, compared to the murine, h
uman and canine C5a receptor sequences, was 85.8, 70.5 and 68.9%, resp
ectively. The greatest diversity exists in the putative extracellular
domains, especially in the aminoterminal domain which is assumed to be
involved in ligand binding. An N-glycosylation site is present within
the N-terminal sequence at residue 6. One of the cDNA containing the
5' untranslated region, the coding sequence and part of the 3' untrans
lated region was cloned into an eucaryotic expression vector and stabl
y transfected into the rat basophilic leukemia cell line RBL-2H3. Expr
ession of the rat C5a receptor on the surface of these cells could be
demonstrated by flow cytometric analysis using FITC-labeled recombinan
t rat C5a (rrC5a). By measuring the release of calcium from intracellu
lar stores after stimulation with rrC5a it could further be shown that
the receptor is functionally coupled. Receptor binding assays showed
that rrC5a specifically binds to the ratC5aR with a K-D of 0.91 +/- 0.
36 and to the human C5a receptor (huCSaR) with a K-D of 7.19 +/- 1.56.
The determined K-D for binding of human C5a (huC5a) to the huC5aR was
2.16 +/- 0.65. No binding of huC5a to the ratC5aR could be observed a
lthough high concentrations of this ligand (> 60 nM) promoted chemotax
is of RBL cells transfected with the huC5aR. (C) 1998 Elsevier Science
Ltd. All rights reserved.