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小鼠前列腺素E受体EP2亚型cDNA的克隆与表达

Cloning and expression of a cDNA for mouse prostaglandin E receptor EP2 subtype.

作者信息

Honda A, Sugimoto Y, Namba T, Watabe A, Irie A, Negishi M, 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 Apr 15;268(11):7759-62.

PMID:8385118
Abstract

A functional cDNA clone encoding mouse EP2 subtype of prostaglandin (PG) E receptor was isolated from a mouse cDNA library by cross-hybridization with the mouse EP3 subtype PGE receptor cDNA. The mouse EP2 receptor consists of 513 amino acid residues with putative seven-transmembrane domains. In contrast to EP3 receptor, this receptor possesses long third intracellular loop and carboxyl-terminal tail. [3H] PGE2 specifically bound to the membrane of mammalian COS cells transfected with the cDNA. The binding to the membrane was displaced with unlabeled PG in the order of PGE2 = PGE1 >> iloprost > or = PGF2 alpha > or = PGD2. The binding was also inhibited by misoprostol, an EP2 and EP3 agonist, but not by sulprostone, an EP1 and EP3 agonist, and SC-19220, an EP1 antagonist. PGE2 markedly increased cAMP level in COS cells transfected with the cDNA. These results suggest that this receptor is EP2 subtype. Northern blot analysis demonstrated that the EP2 mRNA is widely expressed in various tissues, the abundant expression being observed in ileum, thymus, and mastocytoma P-815 cells.

摘要

通过与小鼠EP3亚型前列腺素(PG)E受体cDNA进行交叉杂交,从小鼠cDNA文库中分离出一个编码小鼠前列腺素E受体EP2亚型的功能性cDNA克隆。小鼠EP2受体由513个氨基酸残基组成,具有假定的七跨膜结构域。与EP3受体不同,该受体具有较长的第三细胞内环和羧基末端尾巴。[3H]PGE2特异性结合用该cDNA转染的哺乳动物COS细胞膜。未标记的PG以PGE2 = PGE1 >> 伊洛前列素 ≥ PGF2α ≥ PGD2的顺序取代与膜的结合。米索前列醇(一种EP2和EP3激动剂)也能抑制这种结合,但EP1和EP3激动剂硫前列酮以及EP1拮抗剂SC-19220则不能。PGE2显著提高了用该cDNA转染的COS细胞中的cAMP水平。这些结果表明该受体是EP2亚型。Northern印迹分析表明,EP2 mRNA在各种组织中广泛表达,在回肠、胸腺和肥大细胞瘤P-815细胞中观察到丰富的表达。

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