Alexander Jodi L, Oliphant Andrew, Wilcockson David C, Audsley Neil, Down Rachel E, Lafont Rene, Webster Simon G
School of Biological Sciences, Brambell Laboratories, Bangor University, Bangor, United Kingdom.
Institute of Biological Environmental and Rural Sciences, Aberystwyth University, Aberystwyth, United Kingdom.
Front Neurosci. 2018 Jan 15;11:752. doi: 10.3389/fnins.2017.00752. eCollection 2017.
Neuropeptides play a central role as neurotransmitters, neuromodulators and hormones in orchestrating arthropod physiology. The post-genomic surge in identified neuropeptides and their putative receptors has not been matched by functional characterization of ligand-receptor pairs. Indeed, until very recently no G protein-coupled receptors (GPCRs) had been functionally defined in any crustacean. Here we explore the structurally-related, functionally-diverse gonadotropin-releasing hormone paralogs, corazonin (CRZ) and red-pigment concentrating hormone (RPCH) and their G-protein coupled receptors (GPCRs) in the crab, . Using aequorin luminescence to measure Ca mobilization we demonstrated receptor-ligand pairings of CRZ and RPCH. CRZR-activated cell signaling in a dose-dependent manner (EC 0.75 nM) and comparative studies with insect CRZ peptides suggest that the C-terminus of this peptide is important in receptor-ligand interaction. RPCH interacted with RPCHR with extremely high sensitivity (EC 20 pM). Neither receptor bound GnRH, nor the AKH/CRZ-related peptide. Transcript distributions of both receptors indicate that CRZR expression was, unexpectedly, restricted to the Y-organs (YO). Application of CRZ peptide to YO had no effect on ecdysteroid biosynthesis, excepting a modest stimulation in early post-molt. CRZ had no effect on heart activity, blood glucose levels, lipid mobilization or pigment distribution in chromatophores, a scenario that reflected the distribution of its mRNA. Apart from the well-known activity of RPCH as a chromatophorotropin, it also indirectly elicited hyperglycemia (which was eyestalk-dependent). RPCHR mRNA was also expressed in the ovary, indicating possible roles in reproduction. The anatomy of CRZ and RPCH neurons in the nervous system is described in detail by immunohistochemistry and hybridization. Each peptide has extensive but non-overlapping distribution in the CNS, and neuroanatomy suggests that both are possibly released from the post-commissural organs. This study is one of the first to deorphanize a GPCR in a crustacean and to provide evidence for hitherto unknown and diverse functions of these evolutionarily-related neuropeptides.
神经肽作为神经递质、神经调质和激素,在节肢动物生理调节中发挥着核心作用。在后基因组时代,已鉴定出的神经肽及其假定受体数量激增,但配体 - 受体对的功能表征却未能与之匹配。事实上,直到最近,在任何甲壳类动物中都尚未对G蛋白偶联受体(GPCR)进行功能定义。在此,我们探索了结构相关、功能多样的促性腺激素释放激素旁系同源物、促心肽(CRZ)和红色素聚集激素(RPCH)及其在蟹中的G蛋白偶联受体(GPCR)。我们使用水母发光蛋白发光来测量钙离子动员,证实了CRZ和RPCH的受体 - 配体配对。CRZR以剂量依赖性方式激活细胞信号传导(EC50为0.75 nM),与昆虫CRZ肽的比较研究表明,该肽的C末端在受体 - 配体相互作用中很重要。RPCH与RPCHR的相互作用具有极高的敏感性(EC50为20 pM)。两种受体均不与促性腺激素释放激素(GnRH)或促脂解激素/促心肽相关肽结合。两种受体的转录本分布表明,出乎意料的是,CRZR的表达仅限于Y器官(YO)。将CRZ肽应用于YO对蜕皮甾体生物合成没有影响,除了在蜕皮后早期有适度刺激。CRZ对心脏活动、血糖水平、脂质动员或色素细胞中的色素分布均无影响,这种情况反映了其mRNA的分布。除了众所周知的RPCH作为色素细胞刺激素的活性外,它还间接引发高血糖(这依赖于眼柄)。RPCHR mRNA也在卵巢中表达,表明其在生殖中可能发挥作用。通过免疫组织化学和原位杂交详细描述了神经系统中CRZ和RPCH神经元的解剖结构。每种肽在中枢神经系统中都有广泛但不重叠的分布,神经解剖学表明两者可能都从 commissural 后器官释放。这项研究是首次在甲壳类动物中鉴定孤儿GPCR并为这些进化相关神经肽迄今未知的多样功能提供证据的研究之一。