Novel calcitonin-(8-32)-sensitive adrenomedullin receptors derived from co-expression of calcitonin receptor with receptor activity-modifying proteins

被引:16
作者
Kuwasako, K [1 ]
Kitamura, K [1 ]
Nagoshi, Y [1 ]
Eto, T [1 ]
机构
[1] Miyazaki Med Coll, Dept Internal Med 1, Kiyotake, Miyazaki 8891692, Japan
关键词
adrenomedullin; receptor activity-modifying protein; calcitonin receptor; antagonist; cAMP;
D O I
10.1016/S0006-291X(02)03072-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We tested whether heterodimers comprised of calcitonin (CT) receptor lacking the 16-amino acid insert in intracellular domain 1 (CTR11-) and receptor activity-modifying protein (RAMP) can function not only as calcitonin gene-related peptide (CGRP) receptors but also as adrenomedullin (AM) receptors. Whether transfected alone or together with RAMP, human (h)CTR11- appeared mainly at the surface of HEK-293 cells. Expression of CTR11- alone led to significant increases in cAMP in response to hCGRP or hAM, though both peptides remained about 100-fold less potent than hCT. However, the apparent potency of AM, like that of CGRP, approached that of CT when CTR11- was co-expressed with RAMP. CGRP- or AM-evoked cAMP production was strongly inhibited by salmon CT-(8-32), a selective amylin receptor antagonist, but not by hCGRP-(8-37) or hAM-(22-52), antagonists of CGRP and AM receptors, respectively. Moreover, the inhibitory effects of CT-(8-32) were much stronger in cells co-expressing CTR11- and RAMP than in cells expressing CTR11- alone. Co-expression of CTR11- with RAMP thus appears to produce functional CT-(8-32)-sensitive AM receptors. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:460 / 464
页数:5
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