Receptor activity modifying proteins regulate the activity of a calcitonin gene-related peptide receptor in rabbit aortic endothelial cells

被引:75
作者
Muff, R
Leuthäuser, K
Bühlmann, N
Foord, SM
Fischer, JA
Born, W
机构
[1] Univ Zurich, Dept Orthopaed Surg, Res Lab Calcium Metab, CH-8008 Zurich, Switzerland
[2] Univ Zurich, Dept Med, Res Lab Calcium Metab, CH-8008 Zurich, Switzerland
[3] Glaxo Wellcome Res & Dev Ltd, Med Res Ctr, Receptor Syst Unit, Stevenage SG1 2NY, Herts, England
关键词
neuropeptide; signal transduction; receptor expression; vascular cell;
D O I
10.1016/S0014-5793(98)01587-7
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
In Xenopus oocytes with an endogenous calcitonin gene-related peptide (CGRP) receptor, a receptor activity modifying protein (RAMP1) enhancing CGRP stimulated chloride currents of the cystic fibrosis transmembrane regulator was recently cloned [McLatchie, L.M. et al, (1998) Nature 393, 333-339], Here, transient expression of RAMP1 in rabbit aortic endothelial cells (RAEC) brought about stimulation of cAMP accumulation by human (h) alpha CGRP with an EC50 of 0.41 nM. This was antagonized by a CGRP receptor antagonist alpha CGRP(8-37). Co-expression of RAMP3 together with RAMP1 reduced the maximal cAMP response to h alpha CGRP by 47% (P < 0.05). The cells also express RAMP2 encoding mRNA and an adrenomedullin (ADM) receptor coupled to stimulation of cAMP formation by hADM (EC50 0.18 nM). The latter mas antagonized by an ADM receptor antagonist hADM(22-52). In conclusion, expression of a CGRP receptor in RAEC requires RAMP1. The same receptor presumably recognizes ADM making use of endogenous RAMP2. The results reveal competition between the different RAMPs in the regulation of CGRP/ADM receptor activity. (C) 1998 Federation of European Biochemical Societies.
引用
收藏
页码:366 / 368
页数:3
相关论文
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