Habecker B A, Wang H, Nathanson N M
Department of Pharmacology, University of Washington School of Medicine, Seattle 98195.
Biochemistry. 1993 May 18;32(19):4986-90. doi: 10.1021/bi00070a003.
Muscarinic acetylcholine receptors in the embryonic chicken heart undergo agonist-induced internalization followed by decreases in both receptor number and mRNA expression. Muscarinic agonists cause both inhibition of adenylyl cyclase and activation of phospholipase C in chick heart cells. Treatment of cells with islet activating protein, which blocks coupling of muscarinic receptors to adenylyl cyclase but not phospholipase C, blocks muscarinic receptor-mediated regulation of receptor mRNA levels. Incubation of cells with the partial agonist pilocarpine, which causes inhibition of adenylyl cyclase but not stimulation of phospholipase C, induces less down-regulation of receptor mRNA levels than agonist which regulate both second-messenger systems. Thus, both second-messenger pathways are required for maximal regulation of muscarinic receptor mRNA levels in response to receptor activation. We also demonstrate that the regulation of receptor mRNA by agonist plays an important role in modulating the rate of recovery of muscarinic acetylcholine receptor number following agonist-induced down-regulation.
胚胎期鸡心脏中的毒蕈碱型乙酰胆碱受体在激动剂诱导下会发生内化,随后受体数量和mRNA表达均下降。毒蕈碱型激动剂可抑制鸡心脏细胞中的腺苷酸环化酶并激活磷脂酶C。用可阻断毒蕈碱型受体与腺苷酸环化酶偶联但不阻断与磷脂酶C偶联的百日咳毒素处理细胞,可阻断毒蕈碱型受体介导的受体mRNA水平调节。用可抑制腺苷酸环化酶但不刺激磷脂酶C的部分激动剂毛果芸香碱孵育细胞,与调节两种第二信使系统的激动剂相比,诱导的受体mRNA水平下调较少。因此,两种第二信使途径对于毒蕈碱型受体mRNA水平响应受体激活的最大调节都是必需的。我们还证明,激动剂对受体mRNA的调节在调节激动剂诱导的下调后毒蕈碱型乙酰胆碱受体数量的恢复速率中起重要作用。