Interaction of adrenomedullin with calcitonin receptor in cultured human breast cancer cells, T 47D

被引:16
作者
Disa, J
Dang, K
Tan, KB
Aiyar, N
机构
[1] SmithKline Beecham Pharmaceut, Dept Cardiovasc Pharmacol, King Of Prussia, PA 19406 USA
[2] SmithKline Beecham Pharmaceut, Dept Mol Immunol, King Of Prussia, PA 19406 USA
关键词
adrenomedullin; salmon calcitonin; antagonist; adenylyl cyclase; receptors;
D O I
10.1016/S0196-9781(97)00376-8
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
Human adrenomedullin (hADM), human calcitonin gene-related peptide (hCGRP), and salmon calcitonin (sCT)-activated adenylyl cyclase with EC50, values of 132, 764, and 0.5 nM, respectively, in human breast cancer cell line, T 47D. Treatment of T 47D cell membranes with near maximal concentrations of sCT, hADM and hCGRP had no additive effect on adenylyl cyclase activity. Salmon calcitonin (8-32)(sCT (8-32)), selective antagonist of calcitonin receptor, inhibited the activation of adenylyl cyclase by these three peptides. On the other hand, the putative ADM receptor antagonist, ADM (22-52), and CGRP receptor antagonist, CGRP (8-37), failed to inhibit ADM-, CGRP- or sCT-activated adenylyl cyclase. These results suggest that in T47D cells, both ADM and CGRP activated adenylyl cyclase through sCT receptors. (C) 1998 Elsevier Science Inc.
引用
收藏
页码:247 / 251
页数:5
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