期刊
BIOCHEMICAL PHARMACOLOGY
卷 66, 期 11, 页码 2107-2115出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bcp.2003.07.009
关键词
adrenomedullin; calcitonin gene-related peptide; calcitonin-like receptor; receptor-activity-modifying protein; antagonist
Receptors for calcitonin gene-related peptide (CGRP) and adrenomedullin (AM) are heterodimeric complexes of the calcitonin-like receptor (CLR) together with associated receptor-activity-modifying proteins (RAMP)1, -2 or -3. The RAMP define the specificity of the CLR for CGRP or AM. Here, mouse (m)CLR/mRAMP1, -2 and -3 were expressed in COS-7 cells that lack detectable CGRP and AM receptors. myc epitope-tagged non-glycosylated mRAMP1 required V5-tagged mCLR for its translocation to the cell surface. The glycosylated myc-mRAMP2 and -3, on the other hand, were expressed at the cell surface in the absence of co-transfected mCLR. Selective binding of [I-125]halphaCGRP to mCLR/mRAMP1 expressing cells was inhibited by rat (r)alphaCGRP(1-37) and the CGRP antagonist ralphaCGRP(8-37) with IC50 of 7.0 +/- 1.6 nM and 1.0 +/- 0.1 nM (mean +/- SEM). rAM(1-50) and the AM antagonist rAM(20-50) inhibited [I-125]halphaCGRP binding at over 36-fold higher concentrations than raCGRP. In mCLR/mRAMP2 expressing cells, selective [I-125]rAM binding was inhibited by rAM(1-50) and -(20-50) with IC50 of 8.9 +/- 2.6 nM and 34 +/- 9 nM. ralphaCGRP(1-37) and -(8-37) displaced the binding at over 25-fold higher concentrations. mCLR/mRAMP3 expressing cells recognized both [I-125]halphaCGRP and -rAM. The IC50 of rAM and ralphaCGRP(8-37) ranged between 5.8 and 7.0 nM, and those of ralphaCGRP and rAM(20-50) were only 4- to 8-fold higher. raCGRP and rAM stimulated and ralphaCGRP(8-37) and rAM(20-50) antagonized mCLR/mRAMP1, -2 and -3 mediated cAMP formation with relative potencies that reflected the observed CGRP and AM selectivity of the three receptor types. In conclusion, mCLR/mRAMP1 and -2 are CGRP- and AM-selective receptors, respectively, whereas mCLR/mRAMP3 is an AM/CGRP receptor. (C) 2003 Elsevier Inc. All rights reserved.
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