Farmer S G, Powell S J, Wilkins D E, Graham A
Zeneca Pharmaceuticals, Bioscience, B1124 Research Center, Wilmington, DE 19850, USA.
Eur J Pharmacol. 1998 Apr 10;346(2-3):291-8. doi: 10.1016/s0014-2999(98)00024-7.
Kinin receptors are classified as B1 and B2 based upon agonist and antagonist potencies and cloning and expression studies. Using sequences from human and rat bradykinin B2 receptors, polymerase chain reaction (PCR) was utilized to isolate cDNA from guinea pig lung. The receptor obtained is predicted to have 372 amino acids and shares > 80% sequence homology with human, rat, rabbit and mouse B2 receptors. In competition binding experiments in Chinese hamster ovary (CHO-K1) cells in which the guinea pig cDNA was expressed, [3H]bradykinin was displaced by kinin receptor ligands with an order of potency consistent with a B2 subtype. In CHO cells expressing the guinea pig receptor, bradykinin caused a concentration 45Ca2+ efflux. A B1 receptor agonist, desArg9-bradykinin, also caused 45Ca2+ efflux but with a potency several orders of magnitude lower than bradykinin. Curiously, several B1 and B2 receptor antagonists induced 45Ca2+ efflux, indicating that this receptor may be coupled differently in CHO cells than in native tissues.
根据激动剂和拮抗剂的效力以及克隆和表达研究,激肽受体被分为B1和B2。利用来自人和大鼠缓激肽B2受体的序列,采用聚合酶链反应(PCR)从豚鼠肺中分离出cDNA。所获得的受体预计有372个氨基酸,与人类、大鼠、兔子和小鼠的B2受体具有>80%的序列同源性。在表达豚鼠cDNA的中国仓鼠卵巢(CHO-K1)细胞的竞争结合实验中,[3H]缓激肽被激肽受体配体取代,其效力顺序与B2亚型一致。在表达豚鼠受体的CHO细胞中,缓激肽引起浓度依赖性的45Ca2+外流。一种B1受体激动剂,去精氨酸9-缓激肽,也引起45Ca2+外流,但效力比缓激肽低几个数量级。奇怪的是,几种B1和B2受体拮抗剂诱导45Ca2+外流,表明该受体在CHO细胞中的偶联方式可能与在天然组织中不同。