Johnson G L, Harden T K, Perkins J P
J Biol Chem. 1978 Mar 10;253(5):1465-71.
Human astrocytoma cells (EH118MG) respond to catecholamines and prostaglandins with a marked increase in the rate of formation of cyclic AMP. Treatment of EH118MG cells with cholera toxin (10 to 100 ng/ml) for 45 to 60 min caused an increase in cellular cyclic AMP content (5- to 10-fold over basal). Cholera toxin also decreased the K0.5 for isoproterenol 10- to 50-fold and decreased the K0.5 for prostaglandin E1 (PGE1)30- to 100-fold, while increasing the maximal response to PGE1 by 1.5- to 3-fold. Treatment with cholera toxin did not change the K1 values for beta-adrenergic receptor antagonists such as propranolol, alprenolol, and sotalol. Direct binding studies using [125I]iodohydroxybenzylpindolol indicated no significant changes in the number of beta-receptors or in the kinetics of the interaction of the radioligand with receptors after treatment of cells with the toxin. Competition binding studies with propranolol and sotalol revealed no toxin-induced change in Kd values for these antagonists. Treatment with cholera toxin caused only small decreases (2- to 3-fold) in the Kd values for binding of isoproterenol and norepinephrine. It is concluded that cholera toxin has little direct effect on the binding of agonists or antagonists to beta-receptors, but instead increases the efficiency of coupling of receptor and catalytic moieties of adenylate cyclase.
人星形细胞瘤细胞(EH118MG)对儿茶酚胺和前列腺素产生反应,环磷酸腺苷(cAMP)的生成速率显著增加。用霍乱毒素(10至100纳克/毫升)处理EH118MG细胞45至60分钟,可使细胞内cAMP含量增加(比基础水平高5至10倍)。霍乱毒素还使异丙肾上腺素的半最大效应浓度(K0.5)降低10至50倍,使前列腺素E1(PGE1)的K0.5降低30至100倍,同时使对PGE1的最大反应增加1.5至3倍。用霍乱毒素处理并未改变β-肾上腺素能受体拮抗剂(如普萘洛尔、阿普洛尔和索他洛尔)的K1值。使用[125I]碘羟基苄基吲哚洛尔进行的直接结合研究表明,用毒素处理细胞后,β-受体数量或放射性配体与受体相互作用的动力学没有显著变化。用普萘洛尔和索他洛尔进行的竞争结合研究显示,毒素处理后这些拮抗剂的解离常数(Kd)值没有变化。用霍乱毒素处理仅使异丙肾上腺素和去甲肾上腺素结合的Kd值略有降低(2至3倍)。结论是,霍乱毒素对激动剂或拮抗剂与β-受体的结合几乎没有直接影响,而是增加了受体与腺苷酸环化酶催化部分的偶联效率。