三种G蛋白偶联乙酰胆碱受体在旋毛虫体内的功能表征

IF 4.1 2区 医学 Q1 PARASITOLOGY
Cáinà Nìng, Aurélie Heckmann, Lourdes Mateos-Hernández, Grégory Karadjian , Ladislav Šimo
{"title":"三种G蛋白偶联乙酰胆碱受体在旋毛虫体内的功能表征","authors":"Cáinà Nìng,&nbsp;Aurélie Heckmann,&nbsp;Lourdes Mateos-Hernández,&nbsp;Grégory Karadjian ,&nbsp;Ladislav Šimo","doi":"10.1016/j.ijpddr.2023.11.005","DOIUrl":null,"url":null,"abstract":"<div><p>The physiological significance of metabotropic acetylcholine receptors in parasitic nematodes remains largely unexplored. Here, three different <em>Trichinella spiralis</em> G protein-coupled acetylcholine receptors (TsGAR-1, -2, and -3) were identified in the genome of <em>T</em>. <em>spiralis</em>. The phylogenetic analyses showed that TsGAR-1 and -2 receptors belong to a distinct clade specific to invertebrates, while TsGAR-3 is closest to the cluster of mammalian-type muscarinic acetylcholine receptors (mAChR). The mRNA of TsGAR-1, -2, and -3 was detected in muscle larvae, newborn larvae, and adults. The functional aequorin-based assay in Chinese hamster ovary cells revealed that all three types of <em>T. spiralis</em> GARs trigger the G<sub>q/11</sub> pathway upon activation of the receptor with the acetylcholine ligand. TsGAR-1 and TsGAR-2 showed atypical affinity with classical muscarinic agonists, while TsGAR-3 was sensitive to all muscarinic agonists tested. High concentrations of propiverine antagonist blocked the activities of all three TsGARs, while atropine and scopolamine antagonists effectively inhibited only TsGAR-3. Our data indicate that the distinct pharmacological profile of TsGAR-1 and -2 receptors, as well as the phylogenetic distance between them and their mammalian orthologs, place them as attractive targets for the development of selective anthelmintic drugs interfering with nematodes’ cholinergic system.</p></div>","PeriodicalId":13775,"journal":{"name":"International Journal for Parasitology: Drugs and Drug Resistance","volume":"23 ","pages":"Pages 130-139"},"PeriodicalIF":4.1000,"publicationDate":"2023-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2211320723000386/pdfft?md5=517c5f15c13f7503e708a072bc43584c&pid=1-s2.0-S2211320723000386-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Functional characterization of three G protein-coupled acetylcholine receptors in parasitic nematode Trichinella spiralis\",\"authors\":\"Cáinà Nìng,&nbsp;Aurélie Heckmann,&nbsp;Lourdes Mateos-Hernández,&nbsp;Grégory Karadjian ,&nbsp;Ladislav Šimo\",\"doi\":\"10.1016/j.ijpddr.2023.11.005\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The physiological significance of metabotropic acetylcholine receptors in parasitic nematodes remains largely unexplored. Here, three different <em>Trichinella spiralis</em> G protein-coupled acetylcholine receptors (TsGAR-1, -2, and -3) were identified in the genome of <em>T</em>. <em>spiralis</em>. The phylogenetic analyses showed that TsGAR-1 and -2 receptors belong to a distinct clade specific to invertebrates, while TsGAR-3 is closest to the cluster of mammalian-type muscarinic acetylcholine receptors (mAChR). The mRNA of TsGAR-1, -2, and -3 was detected in muscle larvae, newborn larvae, and adults. The functional aequorin-based assay in Chinese hamster ovary cells revealed that all three types of <em>T. spiralis</em> GARs trigger the G<sub>q/11</sub> pathway upon activation of the receptor with the acetylcholine ligand. TsGAR-1 and TsGAR-2 showed atypical affinity with classical muscarinic agonists, while TsGAR-3 was sensitive to all muscarinic agonists tested. High concentrations of propiverine antagonist blocked the activities of all three TsGARs, while atropine and scopolamine antagonists effectively inhibited only TsGAR-3. Our data indicate that the distinct pharmacological profile of TsGAR-1 and -2 receptors, as well as the phylogenetic distance between them and their mammalian orthologs, place them as attractive targets for the development of selective anthelmintic drugs interfering with nematodes’ cholinergic system.</p></div>\",\"PeriodicalId\":13775,\"journal\":{\"name\":\"International Journal for Parasitology: Drugs and Drug Resistance\",\"volume\":\"23 \",\"pages\":\"Pages 130-139\"},\"PeriodicalIF\":4.1000,\"publicationDate\":\"2023-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2211320723000386/pdfft?md5=517c5f15c13f7503e708a072bc43584c&pid=1-s2.0-S2211320723000386-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal for Parasitology: Drugs and Drug Resistance\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2211320723000386\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PARASITOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal for Parasitology: Drugs and Drug Resistance","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2211320723000386","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PARASITOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

代谢性乙酰胆碱受体在寄生线虫中的生理意义仍未得到充分研究。本研究在旋毛虫基因组中鉴定了三种不同的旋毛虫G蛋白偶联乙酰胆碱受体(TsGAR-1、-2和-3)。系统发育分析表明,TsGAR-1和-2受体属于一个独特的无脊椎动物特异性分支,而TsGAR-3最接近哺乳动物型毒蕈碱乙酰胆碱受体(mAChR)簇。在肌肉幼虫、新生幼虫和成虫中检测到TsGAR-1、-2和-3 mRNA。在中国仓鼠卵巢细胞中进行的功能性黄秋素检测显示,这三种类型的螺旋绦虫GARs都是在乙酰胆碱配体激活受体后触发Gq/11通路的。TsGAR-1和TsGAR-2对经典毒蕈碱激动剂表现出非典型的亲和性,而TsGAR-3对所有毒蕈碱激动剂均敏感。高浓度的丙酸拮抗剂阻断了这三种tsgar的活性,而阿托品和东莨菪碱拮抗剂仅有效抑制TsGAR-3。我们的数据表明,TsGAR-1和-2受体的独特药理学特征,以及它们与哺乳动物同源物之间的系统发育距离,使它们成为开发干扰线虫胆碱能系统的选择性驱虫药的有吸引力的靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Functional characterization of three G protein-coupled acetylcholine receptors in parasitic nematode Trichinella spiralis

Functional characterization of three G protein-coupled acetylcholine receptors in parasitic nematode Trichinella spiralis

The physiological significance of metabotropic acetylcholine receptors in parasitic nematodes remains largely unexplored. Here, three different Trichinella spiralis G protein-coupled acetylcholine receptors (TsGAR-1, -2, and -3) were identified in the genome of T. spiralis. The phylogenetic analyses showed that TsGAR-1 and -2 receptors belong to a distinct clade specific to invertebrates, while TsGAR-3 is closest to the cluster of mammalian-type muscarinic acetylcholine receptors (mAChR). The mRNA of TsGAR-1, -2, and -3 was detected in muscle larvae, newborn larvae, and adults. The functional aequorin-based assay in Chinese hamster ovary cells revealed that all three types of T. spiralis GARs trigger the Gq/11 pathway upon activation of the receptor with the acetylcholine ligand. TsGAR-1 and TsGAR-2 showed atypical affinity with classical muscarinic agonists, while TsGAR-3 was sensitive to all muscarinic agonists tested. High concentrations of propiverine antagonist blocked the activities of all three TsGARs, while atropine and scopolamine antagonists effectively inhibited only TsGAR-3. Our data indicate that the distinct pharmacological profile of TsGAR-1 and -2 receptors, as well as the phylogenetic distance between them and their mammalian orthologs, place them as attractive targets for the development of selective anthelmintic drugs interfering with nematodes’ cholinergic system.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
7.90
自引率
7.50%
发文量
31
审稿时长
48 days
期刊介绍: The International Journal for Parasitology – Drugs and Drug Resistance is one of a series of specialist, open access journals launched by the International Journal for Parasitology. It publishes the results of original research in the area of anti-parasite drug identification, development and evaluation, and parasite drug resistance. The journal also covers research into natural products as anti-parasitic agents, and bioactive parasite products. Studies can be aimed at unicellular or multicellular parasites of human or veterinary importance.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信