Miyauchi K, Tadotsu N, Hayashi T, Ono Y, Tokoyoda K, Tsujikawa K, Yamamoto H
Department of Immunology, Graduate School of Pharmaceutical Sciences, Osaka University, 1-6 Yamadaoka, Suita, Osaka, 565-0871, Japan.
Neuropeptides. 2002 Feb;36(1):22-33. doi: 10.1054/npep.2002.0871.
The calcitonin gene-related peptide (CGRP) plays important roles as a neurotransmitter/neuromodulator in the central nervous system, and as a potent vasodilator when secreted from peripheral, perivascular nerves through its specific receptors. In this study, we cloned mouse cDNA counterparts of the human CGRP receptor composed of calcitonin receptor-like receptor (CRLR) and receptor activity modifying protein 1 (RAMP1) and examined the signal transduction mechanism through the CGRP receptor. Mouse CRLR (mCRLR) is a 462-amino acid G protein-coupled heptahelical receptor, and mouse RAMP1 (mRAMP1) is a 148-amino acid single membrane-spanning protein with a short cytoplasmic portion. Specific binding of (125)I-CGRP was detected only when both mCRLR and mRAMP1 cDNAs were cotransfected to COS-7 cells, and the Kd value of the receptor was 2.2 x 10(-10) M. CGRP induced a marked elevation of the intracellular cAMP levels in COS-7 cells cotransfected with mCRLR and mRAMP1. CGRP signaling through the mCRLR/mRAMP1 receptor complex was found to increase the promoter activities of cyclic AMP responsive element and serum responsive element in the co-transfected HeLa cells. These results indicate that mCRLR and mRAMP1 constitute a functional mouse CGRP receptor for the transduction of CGRP signaling by PKA and extracellular signal-regulated kinase signal transduction pathways.
降钙素基因相关肽(CGRP)在中枢神经系统中作为神经递质/神经调质发挥重要作用,当它从外周血管周围神经通过其特异性受体分泌时,又是一种强效血管舒张剂。在本研究中,我们克隆了由降钙素受体样受体(CRLR)和受体活性修饰蛋白1(RAMP1)组成的人CGRP受体的小鼠cDNA对应物,并研究了通过CGRP受体的信号转导机制。小鼠CRLR(mCRLR)是一种含462个氨基酸的G蛋白偶联七螺旋受体,小鼠RAMP1(mRAMP1)是一种含148个氨基酸的单跨膜蛋白,其胞质部分较短。仅当mCRLR和mRAMP1的cDNA共转染到COS-7细胞时,才能检测到(125)I-CGRP的特异性结合,该受体的Kd值为2.2×10(-10)M。CGRP可使共转染了mCRLR和mRAMP1的COS-7细胞内的cAMP水平显著升高。通过mCRLR/mRAMP1受体复合物的CGRP信号转导在共转染的HeLa细胞中可增加环磷酸腺苷反应元件和血清反应元件的启动子活性。这些结果表明,mCRLR和mRAMP1构成了功能性小鼠CGRP受体,可通过蛋白激酶A和细胞外信号调节激酶信号转导途径转导CGRP信号。