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仓鼠胰岛β细胞中特异性降钙素基因相关肽受体的特性研究

Characterization of specific calcitonin gene-related peptide receptors present in hamster pancreatic beta cells.

作者信息

Barakat A, Rosselin G, Marie J C

机构信息

Institut National de la Santé et de la Recherche Médicale U.55, Hôpital Saint-Antoine, Paris, France.

出版信息

Biosci Rep. 1993 Aug;13(4):221-31. doi: 10.1007/BF01123504.

Abstract

Calcitonin gene-related peptide (CGRP) shares about 46% and 20% amino acid sequence homology with islet amyloid polypeptide (IAPP) and salmon calcitonin (sCT). We investigated whether these related peptides could cross-react with the specific binding of 125I-[His]hCGRP I to the CGRP receptor in hamster insulinoma cell membranes. A rapid dissociation of membrane bound 125I-[His]hCGRP I could be induced in the presence of 1 microM chicken CGRP (cCGRP). The specific 125I-[His]hCGRP I binding was inhibited by the related peptides and their half-maximal inhibitory concentrations (IC50) were: cCGRP (0.1 nM), rat CGRP I and human CGRP I and II (1.0-2.0 nM), fragment of hCGRP I (8-37) (150 nM), human IAPP (440 nM). The non-amidated form of hIAPP; human diabetes-associated peptide (hDAP) did not inhibit the binding of 125I-[His]hCGRP I and sCT was only effective at a high concentration (1 microM). Binding of 125I-[His]hCGRP I was dose dependently inhibited by guanosine-5'-O-(3-thiotriphosphate) or (GTP gamma S) and a 70% reduction of binding was obtained with 0.1 mM GTP gamma S. The IC50 value of cCGRP (0.1 nM) was increased 100-fold in the presence of 0.1 mM GTP gamma S. Human CGRP I and cCGRP at 2.5 microM did not stimulate the activity of hamster insulinoma cell membranes adenylate cyclase, while glucagon (1 microM) induced a 2-fold increase. Thus, specific CGRP receptors present in hamster beta cells are associated with G protein (s) and IAPP can interact with these receptors. These results and the observation that cCGRP and hCGRP I did not influence adenylate cyclase activity provide further evidence for CGRP receptor subtypes.

摘要

降钙素基因相关肽(CGRP)与胰岛淀粉样多肽(IAPP)和鲑鱼降钙素(sCT)的氨基酸序列同源性分别约为46%和20%。我们研究了这些相关肽是否能与125I-[His]hCGRP I与仓鼠胰岛素瘤细胞膜上CGRP受体的特异性结合发生交叉反应。在1微摩尔鸡降钙素(cCGRP)存在的情况下,可诱导膜结合的125I-[His]hCGRP I快速解离。相关肽可抑制125I-[His]hCGRP I的特异性结合,其半数最大抑制浓度(IC50)分别为:cCGRP(0.1纳摩尔)、大鼠CGRP I和人CGRP I及II(1.0 - 2.0纳摩尔)、hCGRP I片段(8 - 37)(150纳摩尔)、人IAPP(440纳摩尔)。人IAPP的非酰胺化形式;人糖尿病相关肽(hDAP)不抑制125I-[His]hCGRP I的结合,而sCT仅在高浓度(1微摩尔)时有效。鸟苷-5'-O-(3-硫代三磷酸)或(GTPγS)可剂量依赖性抑制125I-[His]hCGRP I的结合,0.1毫摩尔GTPγS可使结合减少70%。在0.1毫摩尔GTPγS存在的情况下,cCGRP的IC50值(即抑制一半特异性结合所需的药物浓度)(0.1纳摩尔)增加了100倍。2.5微摩尔的人CGRP I和cCGRP不会刺激仓鼠胰岛素瘤细胞膜腺苷酸环化酶的活性,而胰高血糖素(1微摩尔)可使其活性增加2倍。因此,仓鼠β细胞中存在的特异性CGRP受体与G蛋白相关,且IAPP可与这些受体相互作用。这些结果以及cCGRP和hCGRP I不影响腺苷酸环化酶活性的观察结果为CGRP受体亚型提供了进一步的证据。

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