Heyworth C M, Wallace A V, Houslay M D
Biochem J. 1983 Jul 15;214(1):99-110. doi: 10.1042/bj2140099.
Glucagon (10 nM) caused a transient elevation of intracellular cyclic AMP concentrations, which reached a peak in around 5 min, and slowly returned to basal values in around 30 min. When 1 mM-3-isobutyl-1-methylxanthine (IBMX) was present, this process yielded a Ka of 1 nM for glucagon. The addition of insulin (10 nM) after 5 min exposure to glucagon (10 nM) caused intracellular cyclic AMP concentrations to fall dramatically, attaining basal values within 10 min. The regulation of this process was dose-dependent, exhibiting a Ka of 0.4 nM for insulin. If insulin and glucagon were added together to hepatocytes, then insulin decreased the magnitude of the cyclic AMP response to glucagon. IBMX (1 mM) prevented insulin antagonizing the action of glucagon in both of these instances. A gentle homogenization procedure followed by a rapid subcellular fractionation of hepatocytes on a Percoll gradient was developed. This was used to resolve subcellular membrane fractions and to identify cyclic AMP phosphodiesterase activity in both membrane and cytosol fractions. Glucagon and insulin only affected the activity of two distinct membrane-bound species, a plasma-membrane enzyme and a 'dense vesicle' enzyme. Glucagon (10 nM), insulin (10 nM), IBMX (1 mM), dibutyryl cyclic AMP (10 microM) and cholera toxin (1 microgram/ml) all elicited the activation of the 'dense vesicle' enzyme. The plasma-membrane enzyme was not activated by glucagon, IBMX or dibutyryl cyclic AMP, although insulin and cholera toxin both led to its activation. The degree of activation of the plasma-membrane enzyme produced by insulin was increased in the presence of IBMX or dibutyryl cyclic AMP. Glucagon pretreatment (5 min) of hepatocytes blocked the ability of insulin to activate the plasma-membrane enzyme. The activity state of these phosphodiesterases is discussed in relation to the observed changes in intracellular cyclic AMP concentrations. It is suggested that insulin exerts its action on the plasma-membrane phosphodiesterase through a mechanism involving a guanine nucleotide-regulatory protein.
胰高血糖素(10 nM)可引起细胞内环状AMP浓度短暂升高,约5分钟达到峰值,约30分钟后缓慢恢复至基础值。当存在1 mM - 3 - 异丁基 - 1 - 甲基黄嘌呤(IBMX)时,该过程得到胰高血糖素的解离常数(Ka)为1 nM。在暴露于胰高血糖素(10 nM)5分钟后加入胰岛素(10 nM),可使细胞内环状AMP浓度急剧下降,10分钟内达到基础值。该过程的调节呈剂量依赖性,胰岛素的解离常数(Ka)为0.4 nM。如果将胰岛素和胰高血糖素一起添加到肝细胞中,胰岛素会降低环状AMP对胰高血糖素的反应幅度。在这两种情况下,1 mM的IBMX均可阻止胰岛素拮抗胰高血糖素的作用。开发了一种温和的匀浆程序,随后在Percoll梯度上对肝细胞进行快速亚细胞分级分离。该方法用于分离亚细胞膜组分,并鉴定膜和胞质溶胶组分中的环状AMP磷酸二酯酶活性。胰高血糖素和胰岛素仅影响两种不同的膜结合酶的活性,一种是质膜酶,另一种是“致密囊泡”酶。胰高血糖素(10 nM)、胰岛素(10 nM)、IBMX(1 mM)、二丁酰环状AMP(10 μM)和霍乱毒素(1 μg/ml)均可引起“致密囊泡”酶的激活。尽管胰岛素和霍乱毒素均可导致质膜酶的激活,但胰高血糖素、IBMX或二丁酰环状AMP不会激活质膜酶。在存在IBMX或二丁酰环状AMP的情况下,胰岛素对质膜酶的激活程度会增加。对肝细胞进行胰高血糖素预处理(5分钟)可阻断胰岛素激活质膜酶的能力。结合观察到的细胞内环状AMP浓度变化,讨论了这些磷酸二酯酶的活性状态。研究表明,胰岛素通过涉及鸟嘌呤核苷酸调节蛋白的机制对质膜磷酸二酯酶发挥作用。