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人尤因肉瘤WE-68细胞中降钙素基因相关肽受体的功能特性

Functional characteristics of calcitonin gene-related peptide receptors in human Ewing's sarcoma WE-68 cells.

作者信息

van Valen F, Keck E, Jürgens H

机构信息

Universitätskinderklinik, Abt. für Hämatologie und Onkologie, Düsseldorf, FRG.

出版信息

FEBS Lett. 1989 Oct 9;256(1-2):170-4. doi: 10.1016/0014-5793(89)81742-9.

Abstract

Calcitonin gene-related peptide (CGRP) receptor activity was studied in WE-68 human Ewing's sarcoma cells. 125I-human CGRP bound in a time-dependent, reversible and saturable manner. Scatchard plots were compatible with the presence of a homogenous population of CGRP receptors with high affinity (Kd = 15 pM, and Bmax = 1.9 fmol/mg protein). The potency order of unlabeled peptides in the presence of radioligand, was: human CGRP-II greater than human CGRP = chick CGRP greater than rat CGRP = rat [Tyr0]CGRP greater than human [Tyr0] CGRP much greater than salmon calcitonin (CT) greater than rat [Tyr0]CGRP-(28-37). Each peptide except CT and [Tyr0]CGRP-(28-37) stimulated cyclic AMP generation in a concentration-dependent manner, and the relative potencies paralleled their relative ability in inhibiting 125I-human CGRP binding. We conclude that WE-68 Ewing's sarcoma cells express genuine CGRP receptors which upon activation lead to stimulation of cyclic AMP formation

摘要

在WE - 68人尤因肉瘤细胞中研究了降钙素基因相关肽(CGRP)受体活性。125I - 人CGRP以时间依赖性、可逆性和饱和性方式结合。Scatchard图与存在具有高亲和力的同质性CGRP受体群体(Kd = 15 pM,Bmax = 1.9 fmol/mg蛋白质)相符。在存在放射性配体的情况下,未标记肽的效价顺序为:人CGRP - II>人CGRP = 鸡CGRP>大鼠CGRP = 大鼠[Tyr0]CGRP>人[Tyr0]CGRP>>鲑鱼降钙素(CT)>大鼠[Tyr0]CGRP - (28 - 37)。除CT和[Tyr0]CGRP - (28 - 37)外,每种肽均以浓度依赖性方式刺激环磷酸腺苷生成,且相对效价与其抑制125I - 人CGRP结合的相对能力平行。我们得出结论,WE - 68尤因肉瘤细胞表达真正的CGRP受体,其激活后会刺激环磷酸腺苷的形成

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