Takeuchi K, Abe T, Takahashi N, Abe K
Second Department of Internal Medicine, Tohoku University School of Medicine, Sendai, Japan.
Biochem Biophys Res Commun. 1993 Jul 30;194(2):885-91. doi: 10.1006/bbrc.1993.1904.
A rat kidney cDNA library was screened with a mouse prostaglandin (PG) E2 receptor EP3 alpha subtype cDNA as a probe, and a 2.2-kilobase pair cDNA was isolated. The cDNA encodes 365 amino acids with 97.0% sequence identity to mouse EP3 alpha receptor. Specific binding of [3H]PGE2 was found in COS-7 cells transfected with the cDNA (Kd = 3.2nM) and was displaced with unlabeled prostaglandins in the order of PGE2 = PGE1 >> PGF2 alpha > PGD2. Thus, a cDNA for rat EP3 (rEP3) receptor was cloned. In situ hybridization revealed expression of rEP3 receptor principally in tubules of renal medulla. Consistent with this observation, the reverse transcription and polymerase chain reaction (RT-PCR) technique using dissected nephron segments showed the receptor expression specifically in medullary thick ascending limbs of Henle's loop (mTAL), cortical TAL (cTAL), cortical collecting ducts (CCD) and inner medullary collecting ducts (IMCD), indicating a possible diuretic and natriuretic role of rEP3 receptor at the distal nephron segments.
以小鼠前列腺素(PG)E2受体EP3α亚型cDNA为探针筛选大鼠肾cDNA文库,分离出一个2.2千碱基对的cDNA。该cDNA编码365个氨基酸,与小鼠EP3α受体的序列同一性为97.0%。在用该cDNA转染的COS-7细胞中发现了[3H]PGE2的特异性结合(Kd = 3.2nM),并且未标记的前列腺素以PGE2 = PGE1 >> PGF2α > PGD2的顺序取代了它。因此,克隆了大鼠EP3(rEP3)受体的cDNA。原位杂交显示rEP3受体主要在肾髓质的小管中表达。与这一观察结果一致,使用解剖的肾单位节段的逆转录聚合酶链反应(RT-PCR)技术显示该受体在亨氏袢髓质厚升支(mTAL)、皮质TAL(cTAL)、皮质集合管(CCD)和内髓质集合管(IMCD)中特异性表达,表明rEP3受体在远端肾单位节段可能具有利尿和排钠作用。