Brown M, Webb M, Phillips E, Skidmore E, McIntyre P
Sandoz Institute for Medical Research, London, United Kingdom.
Can J Physiol Pharmacol. 1995 Jul;73(7):780-6. doi: 10.1139/y95-105.
We describe the results of functional studies on DNA clones encoding functional bradykinin receptors derived from human, rat, and mouse sources and including both genomic and complementary DNA clones. In both the Xenopus oocyte and the COS cell expression systems, the receptors from human and rat showed the pharmacological properties of B2 receptors, but receptors from mouse displayed both B1- and B2-like pharmacological properties. We further investigated the molecular relationship between the B1 and B2 receptor subtypes expressed by a human fibroblast cell line, and we demonstrate that these two receptor subtypes are encoded by distinct mRNA species.
我们描述了对编码源自人、大鼠和小鼠的功能性缓激肽受体的DNA克隆进行功能研究的结果,这些克隆包括基因组DNA克隆和互补DNA克隆。在非洲爪蟾卵母细胞和COS细胞表达系统中,人和大鼠的受体表现出B2受体的药理学特性,但小鼠的受体表现出B1和B2样药理学特性。我们进一步研究了人成纤维细胞系表达的B1和B2受体亚型之间的分子关系,并证明这两种受体亚型由不同的mRNA种类编码。