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前列腺素E受体小鼠EP1亚型cDNA的克隆与表达

Cloning and expression of cDNA for a mouse EP1 subtype of prostaglandin E receptor.

作者信息

Watabe A, Sugimoto Y, Honda A, Irie A, Namba T, Negishi M, Ito S, Narumiya S, Ichikawa A

机构信息

Department of Physiological Chemistry, Faculty of Pharmaceutical Sciences, Kyoto University, Japan.

出版信息

J Biol Chem. 1993 Sep 25;268(27):20175-8.

PMID:7690750
Abstract

A functional cDNA clone encoding a mouse EP1 subtype of prostaglandin (PG) E receptor was isolated from a mouse cDNA library by cross-hybridization with the mouse thromboxane A2 receptor cDNA. The clone isolated encodes a protein consisting of 405 amino acid residues with putative seven-transmembrane domains. [3H]PGE2 specifically bound to the membrane of Chinese hamster ovary cells expressing this clone. The binding to the membrane was displaced with unlabeled PGs in the order of PGE2 > iloprost (a prostacyclin analogue) > PGE1 > PGF2 alpha > U-46619 (a thromboxane A2 analogue) > PGD2. The binding was also inhibited by 17-phenyl trinor PGE2 (an EP1 agonist) and sulprostone (an EP1 and EP3 agonist) but not by 11-deoxy PGE1 (an EP2 and EP3 agonist) and butaprost (an EP2 agonist). PGE2 induced a rapid increase in intracellular Ca2+ concentration in Chinese hamster ovary cells expressing the receptor. These results suggest that this receptor belongs to EP1 subtype of PGE receptor. Northern blot analysis demonstrated that the mRNA of this receptor is expressed abundantly in kidney and in a lessor amount in lung.

摘要

通过与小鼠血栓素A2受体cDNA进行交叉杂交,从小鼠cDNA文库中分离出一个编码前列腺素(PG)E受体小鼠EP1亚型的功能性cDNA克隆。分离得到的克隆编码一种由405个氨基酸残基组成的蛋白质,具有假定的七个跨膜结构域。[3H]PGE2特异性结合表达该克隆的中国仓鼠卵巢细胞的膜。与膜的结合被未标记的PGs以PGE2>伊洛前列素(一种前列环素类似物)>PGE1 > PGF2α>U-46619(一种血栓素A2类似物)>PGD2的顺序取代。该结合也受到17-苯基三降PGE2(一种EP1激动剂)和舒前列素(一种EP1和EP3激动剂)的抑制,但不受11-脱氧PGE1(一种EP2和EP3激动剂)和布他前列素(一种EP2激动剂)的抑制。PGE2诱导表达该受体的中国仓鼠卵巢细胞内Ca2+浓度迅速升高。这些结果表明该受体属于PGE受体的EP1亚型。Northern印迹分析表明,该受体的mRNA在肾脏中大量表达,在肺中表达量较少。

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