Literature DB >> 12807445

Characterization of a novel G-protein coupled receptor from the parasitic nematode H. contortus with high affinity for serotonin.

Martin W Smith1, Tracy L Borts, Renee Emkey, Carolyn A Cook, Christina J Wiggins, Jesus A Gutierrez.   

Abstract

The neurotransmitter serotonin (5HT) has been shown to modulate mobility, feeding, egg-laying, and defecation behaviors in the saprophytic nematode Caenorhabditis elegans. Although the effects of serotonin on these behaviors in parasitic nematodes is under study, little is known about the diversity, ontogeny, signaling, and pharmacology of serotonin receptors in these organisms. In an effort to increase our understanding of this system, we cloned and characterized a novel cDNA (5HT1Hc) from the parasitic nematode Haemonchus contortus that has high amino acid sequence homology with known G-protein coupled 5HT1-receptors from invertebrates and vertebrates. Transcript expression studies in four development stages (egg, L1/L2, L3, and adult) revealed the presence of the mRNA in the L1/L2, L3, and adult stages. Membranes from insect cells (Sf9) expressing the 5HT1Hc-receptor cDNA displayed nanomolar binding affinity to serotonin and a unique pharmacological profile distinct from known invertebrate and mammalian 5HT-receptors. Receptor signaling studies with mammalian AV12 cells expressing the 5HT1Hc-receptor and the promiscuous G-protein, Galpha15, demonstrated dose-dependent intracellular signals with serotonin acting as an agonist. Together, these studies describe a novel invertebrate 5HT-receptor with high affinity for the indolealkylamine, serotonin, and pharmacological properties that do not conform to any known members of this superfamily of metabotropic receptors.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12807445     DOI: 10.1046/j.1471-4159.2003.01849.x

Source DB:  PubMed          Journal:  J Neurochem        ISSN: 0022-3042            Impact factor:   5.372


  5 in total

1.  Ionic liquid-supported synthesis of piperazine derivatives as potential insecticides.

Authors:  Yan Shen; Jia-Yi Wang; Gong-Hua Song
Journal:  Mol Divers       Date:  2013-11-27       Impact factor: 2.943

Review 2.  Ion channels and receptor as targets for the control of parasitic nematodes.

Authors:  Adrian J Wolstenholme
Journal:  Int J Parasitol Drugs Drug Resist       Date:  2011-10-14       Impact factor: 4.077

Review 3.  Monoaminergic signaling as a target for anthelmintic drug discovery: receptor conservation among the free-living and parasitic nematodes.

Authors:  Richard Komuniecki; Wen Jing Law; Aaron Jex; Peter Geldhof; John Gray; Bruce Bamber; Robin B Gasser
Journal:  Mol Biochem Parasitol       Date:  2012-02-11       Impact factor: 1.759

4.  Are Caenorhabditis elegans receptors useful targets for drug discovery: pharmacological comparison of tyramine receptors with high identity from C. elegans (TYRA-2) and Brugia malayi (Bm4).

Authors:  Katherine A Smith; Elizabeth B Rex; Richard W Komuniecki
Journal:  Mol Biochem Parasitol       Date:  2007-04-13       Impact factor: 1.759

5.  Heterologous Expression in Remodeled C. elegans: A Platform for Monoaminergic Agonist Identification and Anthelmintic Screening.

Authors:  Wenjing Law; Leah M Wuescher; Amanda Ortega; Vera M Hapiak; Patricia R Komuniecki; Richard Komuniecki
Journal:  PLoS Pathog       Date:  2015-04-30       Impact factor: 6.823

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.