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胰岛素分泌细胞系RINm5F表达α-2D肾上腺素能受体和非肾上腺素能咪唑克生结合位点。

The insulin-secreting cell line, RINm5F, expresses an alpha-2D adrenoceptor and nonadrenergic idazoxan-binding sites.

作者信息

Remaury A, Paris H

机构信息

I.N.S.E.R.M., Institut de Physiologie, Toulouse, France.

出版信息

J Pharmacol Exp Ther. 1992 Jan;260(1):417-26.

PMID:1346166
Abstract

The pharmacological properties of alpha-2 adrenoceptors and the existence of nonadrenergic idazoxan-binding sites (NAIBS) were investigated in the insulin-secreting cell-line, RINm5F, using [3H]RX821002 and [3H]idazoxan. Analysis of [3H]RX821002 saturation isotherms revealed the presence of a single class of binding sites (Bmax = 47.5 +/- 3.5 fmol/mg protein) having high affinity (Kd = 1.26 +/- 0.18 nM). Inhibition of [3H]RX821002 binding by adrenergic compounds showed that the labeled sites displayed the properties expected for an alpha-2 adrenoceptor. Based on competition data with drugs having alpha-2 adrenoceptor subtype selectivity, the receptor from RINm5F is neither an alpha-2B nor an alpha-2C. It resembles the alpha-2A, but deviates from this subtype because of a weak affinity for yohimbine and rauwolscine. In this respect, RINm5F alpha-2 adrenoceptor is identical to the receptor previously described in rat intestinal mucosa and corresponds to a fourth subtype: alpha-2D. Agonist inhibition curves were better fitted by a two-site model and indicated that about half of the receptor population was under a high-affinity state corresponding to G protein-coupled receptors. [32P]ADP-ribosylation with pertussis toxin and immunodetection with specific antibodies permitted the identification of three distinct G proteins: Gi2, Gi3 and G0. Binding experiments with [3H]idazoxan showed that this imidazoline labeled two types of sites corresponding to alpha-2 adrenoceptors and NAIBS. Analysis of saturation isotherms under binding conditions allowing to discriminate between the two site populations indicated that the density of NAIBS (44 +/- 2 fmol/mg protein) was fairly identical to that of alpha-2 adrenoceptors. The pharmacological properties of NAIBS, as assessed by determining the relative affinity of imidazolinic and nonimidazolinic compounds, reasonably matched that reported in other tissues. Taken together, these data make the RINm5F cell-line 1) the first model in permanent culture known as expressing an alpha-2 adrenoceptor of the alpha-2D subtype; 2) a good system for studying in vitro the respective role of alpha-2 adrenoceptors and NAIBS in the regulation of insulin secretion by beta cells.

摘要

利用[3H]RX821002和[3H]咪唑克生,在胰岛素分泌细胞系RINm5F中研究了α-2肾上腺素能受体的药理学特性以及非肾上腺素能咪唑克生结合位点(NAIBS)的存在情况。对[3H]RX821002饱和等温线的分析显示存在一类单一的结合位点(Bmax = 47.5 +/- 3.5 fmol/mg蛋白质),具有高亲和力(Kd = 1.26 +/- 0.18 nM)。肾上腺素能化合物对[3H]RX821002结合的抑制作用表明,标记位点表现出α-2肾上腺素能受体预期的特性。基于与具有α-2肾上腺素能受体亚型选择性的药物的竞争数据,RINm5F的受体既不是α-2B也不是α-2C。它类似于α-2A,但由于对育亨宾和萝芙木碱的亲和力较弱而偏离该亚型。在这方面,RINm5Fα-2肾上腺素能受体与先前在大鼠肠黏膜中描述的受体相同,对应于第四种亚型:α-2D。激动剂抑制曲线用双位点模型拟合得更好,表明约一半的受体群体处于与G蛋白偶联受体相对应的高亲和力状态。用百日咳毒素进行[32P]ADP-核糖基化和用特异性抗体进行免疫检测,可鉴定出三种不同的G蛋白:Gi2、Gi3和G0。用[3H]咪唑克生进行的结合实验表明,这种咪唑啉标记了与α-2肾上腺素能受体和NAIBS相对应的两种类型的位点。在允许区分两个位点群体的结合条件下对饱和等温线的分析表明,NAIBS的密度(44 +/- 2 fmol/mg蛋白质)与α-2肾上腺素能受体的密度相当。通过测定咪唑啉类和非咪唑啉类化合物的相对亲和力评估的NAIBS的药理学特性,与其他组织中报道的特性合理匹配。综上所述,这些数据使RINm5F细胞系成为:1)第一个已知表达α-2D亚型α-2肾上腺素能受体的永久培养模型;2)一个用于体外研究α-2肾上腺素能受体和NAIBS在β细胞胰岛素分泌调节中各自作用的良好系统。

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