Angers A, Storozhuk M V, Duchaîne T, Castellucci V F, DesGroseillers L
Département de biochimie, Université de Montréal, Montréal, Québec, Canada H3C 3J7.
J Neurosci. 1998 Aug 1;18(15):5586-93. doi: 10.1523/JNEUROSCI.18-15-05586.1998.
Serotonin (5-HT) is involved in the control of various behaviors in Aplysia californica, including reproduction, feeding, locomotion, circadian rhythm, synaptic plasticity, and synaptic growth. The large variety of functions of 5-HT is mediated by different receptor subtypes that are coupled to different second-messenger systems. Here, we report the cloning of a cDNA coding for an Aplysia G-protein-coupled 5-HT receptor (5-HTap1). Its deduced amino acid sequence resembles those of the 5-HT1 receptor subfamily. When expressed in stable cell lines, 5-HTap1 exhibits high-affinity binding for the serotonergic radioligand [N-methyl-3H]lysergic acid diethylamide. This binding is competed by several 5-HT agonists and antagonists, and the pharmacological profile of inhibition has some similarities with those of 5-HT1 and 5-HT7 receptors. Application of 5-HT or its agonists 5-carboxamidotryptamine maleate and (+/-)-8-hydroxy-2-(di-n-propyl-amino) tetralin hydrobromide on cells transformed with 5-HTap1 produced a dose-dependent inhibition of forskolin-stimulated cAMP accumulation. 5-HTap1 is thus negatively coupled to adenylate cyclase. The production of antiserum against the 5-HTap1 receptor allowed us to examine its expression in animal tissues. The receptor protein is detected in every tissue examined, although it seems only weakly expressed in some samples. The receptor is also found in every ganglia of the nervous system, both in the sheath and in the neurons. 5-HTap1 mRNA is absent from the sheath, indicating that the protein observed there is probably located on the nerve terminals.
血清素(5-羟色胺,5-HT)参与调控加州海兔的多种行为,包括繁殖、进食、运动、昼夜节律、突触可塑性和突触生长。5-HT的多种功能是由与不同第二信使系统偶联的不同受体亚型介导的。在此,我们报告了一个编码加州海兔G蛋白偶联5-HT受体(5-HTap1)的cDNA的克隆。其推导的氨基酸序列与5-HT1受体亚家族的序列相似。当在稳定细胞系中表达时,5-HTap1对血清素能放射性配体[甲基-3H]麦角酸二乙酰胺表现出高亲和力结合。这种结合被几种5-HT激动剂和拮抗剂竞争,并且抑制的药理学特征与5-HT1和5-HT7受体的特征有一些相似之处。将5-HT或其激动剂马来酸5-羧酰胺色胺和(±)-8-羟基-2-(二正丙基氨基)四氢萘氢溴酸盐应用于用5-HTap1转化的细胞,产生了对福斯高林刺激的环磷酸腺苷(cAMP)积累的剂量依赖性抑制。因此,5-HTap1与腺苷酸环化酶负偶联。针对5-HTap1受体产生的抗血清使我们能够检测其在动物组织中的表达。在所检查的每个组织中都检测到了受体蛋白,尽管在一些样品中它似乎表达较弱。在神经系统的每个神经节中,无论是在神经鞘还是在神经元中都发现了该受体。神经鞘中不存在5-HTap1 mRNA,这表明在那里观察到的蛋白质可能位于神经末梢上。