The cloning of AT1 and AT2 receptors reveals they are seven transmembrane domain receptors with distinct signaling mechanisms, including AT2's unique pertussis toxin-sensitive inhibition of phosphotyrosine phosphatase.
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Defines receptor signaling in recombinant systems; leaves open translation to cardiovascular disease models or therapies.
Angiotensin II isoform 1 (AT1) receptor cDNAs were cloned by expression cloning from bovine adrenal and rat vascular smooth muscles. Human AT1 receptor was also cloned. Seven transmembrane structures emerged. A single type of receptor seems to interact with more than one type of G-protein. AT1 consists of subtypes AT1A and AT1B, and the regulation of the receptors occurs at many stages. The isoform AT2 was also expression cloned from rat pheochromocytoma cells. Although its ligand binding is not affected by GTP analogs, it is a seven transmembrane domain receptor. It mediates the inhibition of phosphotyrosine phosphatase by angiotensin II and AT2 specific CGP42112A; the inhibition was abolished by pertussis toxin. Thus, AT2 belongs to a new class of angiotensin receptors with unique signalling and regulatory mechanisms.
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Inagami et al. (1994) studied this question.
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