Hirata M, Kakizuka A, Aizawa M, Ushikubi F, Narumiya S
Department of Pharmacology, Kyoto University Faculty of Medicine, Japan.
Proc Natl Acad Sci U S A. 1994 Nov 8;91(23):11192-6. doi: 10.1073/pnas.91.23.11192.
Prostanoid receptors belong to the family of G protein-coupled receptors with seven transmembrane domains. By taking advantage of nucleotide sequence homology among the prostanoid receptors, we have isolated and identified a cDNA fragment and its gene encoding a mouse prostaglandin (PG) D receptor by reverse transcription polymerase chain reaction and gene cloning. This gene codes for a polypeptide of 357 amino acids, with a calculated molecular weight of 40,012. The deduced amino acid sequence has a high degree of similarity with the mouse PGI receptor and the EP2 subtype of the PGE receptor, which together form a subgroup of the prostanoid receptors. Chinese hamster ovary cells stably expressing the gene showed a single class of binding sites for [#H]PGD2 with a Kd of 40 nM. This binding was displaced by unlabeled ligands in the following order: PGD2 > BW 245C (a PGD agonist) > BW A868C (a PGD antagonist) > STA2 (a thromboxane A2 agonist). PGE2, PGF2 alpha, and iloprost showed little displacement activity at concentrations up to 10 microM. PGD2 and BW 245C also increased cAMP levels in Chinese hamster ovary cells expressing the receptor, in a concentration-dependent manner. BW A868C showed a partial agonist activity in the cAMP assay. Northern blotting analysis with mouse poly(A)+ RNA identified a major mRNA species of 3.5 kb that was most abundantly expressed in the ileum, followed by lung, stomach, and uterus.
前列腺素受体属于具有七个跨膜结构域的G蛋白偶联受体家族。利用前列腺素受体之间的核苷酸序列同源性,我们通过逆转录聚合酶链反应和基因克隆分离并鉴定了一个编码小鼠前列腺素(PG)D受体的cDNA片段及其基因。该基因编码一个由357个氨基酸组成的多肽,计算分子量为40,012。推导的氨基酸序列与小鼠PGI受体和PGE受体的EP2亚型具有高度相似性,它们共同构成前列腺素受体的一个亚组。稳定表达该基因的中国仓鼠卵巢细胞显示出一类对[#H]PGD2的结合位点,Kd为40 nM。这种结合被未标记的配体按以下顺序取代:PGD2 > BW 245C(一种PGD激动剂)> BW A868C(一种PGD拮抗剂)> STA2(一种血栓素A2激动剂)。PGE2、PGF2α和伊洛前列素在浓度高达10 μM时显示出几乎没有取代活性。PGD2和BW 245C也以浓度依赖的方式增加表达该受体的中国仓鼠卵巢细胞中的cAMP水平。BW A868C在cAMP测定中显示出部分激动剂活性。用小鼠聚腺苷酸加尾RNA进行的Northern印迹分析鉴定出一种主要的3.5 kb mRNA种类,其在回肠中表达最丰富,其次是肺、胃和子宫。