Inagami T, Yamano Y, Bardhan S, Chaki S, Guo D F, Ohyama K, Kambayashi Y, Takahashi K, Ichiki T, Tsuzuki S
Department of Biochemistry, Vanderbilt University School of Medicine, Nashville, Tennessee 37232-0146, USA.
Adv Exp Med Biol. 1995;377:311-7. doi: 10.1007/978-1-4899-0952-7_21.
Complementary DNAs for angiotensin II type 1 receptor isoforms AT1A and AT1B were cloned by expression cloning from bovine adrenal and rat vascular smooth muscles. Human AT1 receptor was also cloned. Seven transmembrane structures emerged. The AT1 type receptor interacted with more than one type of G-proteins. The ligand binding site of AT1 involving Arg167, Lys199, and Asp263 has been identified by site directed mutagenesis. The regulation of the receptors occur at many stages. The isoform, AT2, was also expression cloned from rat pheochromocytoma cells. Although its ligand binding is not affected by stable GTP analogs, it is a seven transmembrane domain receptor. It mediates the modulations of phosphotyrosine phosphatase by angiotensin II and AT2 specific CGP42112A. The modulation was abolished by pertussis toxin. Thus, AT2 belongs to a new class of angiotensin receptors with unique signalling and regulatory mechanisms. AT1 mediates cellular growth. Interestingly, AT2 expression is inversely related to the mitogenic activity of cells.
通过从牛肾上腺和大鼠血管平滑肌中进行表达克隆,获得了血管紧张素II 1型受体亚型AT1A和AT1B的互补DNA。人AT1受体也被克隆出来。发现了七个跨膜结构。AT1型受体与不止一种类型的G蛋白相互作用。通过定点诱变确定了AT1的配体结合位点涉及精氨酸167、赖氨酸199和天冬氨酸263。受体的调节发生在多个阶段。亚型AT2也从大鼠嗜铬细胞瘤细胞中通过表达克隆获得。尽管其配体结合不受稳定GTP类似物的影响,但它是一个七跨膜结构域受体。它介导血管紧张素II和AT2特异性的CGP42112A对磷酸酪氨酸磷酸酶的调节。这种调节被百日咳毒素消除。因此,AT2属于一类具有独特信号传导和调节机制的新型血管紧张素受体。AT1介导细胞生长。有趣的是,AT2的表达与细胞的促有丝分裂活性呈负相关。