Jansson C C, Savola J M, Akerman K E
Department of Biochemistry and Pharmacy, BioCity, Abo Akademi University, Turku, Finland.
Biochem Biophys Res Commun. 1994 Mar 15;199(2):869-75. doi: 10.1006/bbrc.1994.1309.
Two human alpha 2-adrenergic receptor subtypes, alpha 2A-C10 and alpha 2C-C4, were compared with respect to their ability to inhibit stimulated cAMP-production. The inhibition was transduced with about one order of magnitude higher sensitivity in the alpha 2C-C4 subtype than in the alpha 2A-C10 subtype. The phorbol ester, TPA, known to desensitize alpha 2-adrenergic receptor function, possible through phosphorylation of Gi, almost completely abolished the inhibition of cAMP-production in the alpha 2C-C4 subtype, while only a partial effect was seen in the alpha 2A-C10 subtype. These results suggest that the receptor subtypes differ with respect to their coupling efficiency to adenylyl cyclase.
对两种人类α2 - 肾上腺素能受体亚型α2A - C10和α2C - C4抑制刺激型cAMP生成的能力进行了比较。在α2C - C4亚型中,这种抑制作用的转导敏感性比α2A - C10亚型高约一个数量级。佛波酯TPA已知可使α2 - 肾上腺素能受体功能脱敏,可能是通过Gi的磷酸化,它几乎完全消除了α2C - C4亚型中cAMP生成的抑制作用,而在α2A - C10亚型中仅观察到部分作用。这些结果表明,受体亚型在与腺苷酸环化酶的偶联效率方面存在差异。