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人类A1腺苷受体:配体结合特性、体细胞表达位点及染色体定位

The human A1 adenosine receptor: ligand binding properties, sites of somatic expression and chromosomal localization.

作者信息

Rivkees S A, Lasbury M E, Stiles G S, Henegariu O, Curtis C, Vance G

机构信息

Section of Pediatric Endocrinology, Herman B Wells Center for Pediatric Research, 46202, Indianapolis, Indiana, USA.

出版信息

Endocrine. 1995 Sep;3(9):623-9. doi: 10.1007/BF02746338.

Abstract

The A1 adenosine receptor (A1AR) exerts important biological effects in the mammalian biology. To provide insights into the role A1AR action in human physiology, we characterized the pharmacologic properties of the human A1AR, examined somatic sites of A1AR gene expression, and identified the chromosomal location of the human A1AR gene. Using stably transfected CHO cells, the ligand binding properties of human and rat A1ARs were directly compared. Saturation studies showed that the human and rat A1ARs had similar high affinity for the A1 agonist [(3)H]CCPA (human, K(d)=517±64 pM; B(max) 438±29 fmol/mg of protein; rat, K(d)=429±69 pM; B(max) 358±76 fmol/mg of protein). Competition studies performed using seven adenosine agonists and four adenosine antagonists also did not detect differences in the ligand binding properties among the rat and human A1ARs. Northern analysis of 16 human tissues revealed the presence of a single hybridizing transcript of 2.5 kb. Human A1AR receptor mRNA expression was greatest in brain and testis; lower levels of A1AR mRNA were present in heart, pancreas, kidney and spleen. Southern blotting and PCR analysis of human-rodent somatic cell hybrids showed that the A1AR gene is on human chromosome 1. Using fluorescence in situ hybridization, the human A1AR gene was further localized to the 1q32.1 region. These observations show that the human A1AR is a high affinity receptor that has ligand binding properties similar to the rat A1AR, human A1AR mRNA is heavily expressed in brain and testis, and the gene encoding the human A1AR is present on the long arm of chromosome 1.

摘要

A1 腺苷受体(A1AR)在哺乳动物生物学中发挥着重要的生物学作用。为深入了解 A1AR 作用在人类生理学中的角色,我们对人 A1AR 的药理学特性进行了表征,研究了 A1AR 基因表达的体细胞位点,并确定了人 A1AR 基因的染色体定位。利用稳定转染的 CHO 细胞,直接比较了人和大鼠 A1AR 的配体结合特性。饱和研究表明,人和大鼠 A1AR 对 A1 激动剂[(3)H]CCPA 具有相似的高亲和力(人,K(d)=517±64 pM;B(max) 438±29 fmol/mg 蛋白质;大鼠,K(d)=429±69 pM;B(max) 358±76 fmol/mg 蛋白质)。使用七种腺苷激动剂和四种腺苷拮抗剂进行的竞争研究也未检测到大鼠和人 A1AR 之间配体结合特性的差异。对 16 种人类组织的 Northern 分析显示存在一个 2.5 kb 的单一杂交转录本。人 A1AR 受体 mRNA 表达在脑和睾丸中最高;心脏、胰腺、肾脏和脾脏中 A1AR mRNA 水平较低。对人-啮齿动物体细胞杂种的 Southern 印迹和 PCR 分析表明,A1AR 基因位于人类染色体 1 上。利用荧光原位杂交,人 A1AR 基因进一步定位到 1q32.1 区域。这些观察结果表明,人 A1AR 是一种高亲和力受体,其配体结合特性与大鼠 A1AR 相似,人 A1AR mRNA 在脑和睾丸中大量表达,编码人 A1AR 的基因位于染色体 1 的长臂上。

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