{"title":"鉴定泥蟹Scylla paramamosain中的ETH受体及其可能的作用。","authors":"","doi":"10.1016/j.cbpa.2024.111692","DOIUrl":null,"url":null,"abstract":"<div><p>Ecdysis-triggering hormone (ETH) is a neuropeptide hormone characterized by a conserved KxxKxxPRx amide structure widely identified in arthropods. While its involvement in the regulation of molting and reproduction in insects is well-established, its role in crustaceans has been overlooked. This study aimed to de-orphanise a receptor for ETH in the mud crab <em>Scylla paramamosain</em> and explore its potential impact on ovarian development. A 513-amino-acid G protein-coupled receptor for ETH (<em>Sp</em>ETHR) was identified in <em>S. paramamosain</em>, exhibiting a dose-dependent activation by <em>Sp</em>ETH with an EC<sub>50</sub> value of 75.18 nM. Tissue distribution analysis revealed <em>SpETH</em> was in the cerebral ganglion and thoracic ganglion, while <em>SpETHR</em> was specifically expressed in the ovary, hepatopancreas, and Y-organ of female crabs. <em>In vitro</em> experiments demonstrated that synthetic <em>Sp</em>ETH (at a concentration of 10<sup>−8</sup> M) significantly increased the expression of <em>SpVgR</em> in the ovary and induced ecdysone biosynthesis in the Y-organ. <em>In vivo</em> experiments showed a significant upregulation of <em>SpEcR</em> in the ovary and <em>Disembodied</em> and <em>Shadow</em> in the Y-organ after 12 h of <em>Sp</em>ETH injection. Furthermore, a 16-day administration of <em>Sp</em>ETH significantly increased 20E titers in hemolymph, gonadosomatic index (GSI) and oocyte size of <em>S. paramamosain.</em> In conclusion, our findings suggest that <em>Sp</em>ETH may play stimulatory roles in ovarian development and ecdysone biosynthesis by the Y-organ.</p></div>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2024-07-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Identification of ETH receptor and its possible roles in the mud crab Scylla paramamosain\",\"authors\":\"\",\"doi\":\"10.1016/j.cbpa.2024.111692\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Ecdysis-triggering hormone (ETH) is a neuropeptide hormone characterized by a conserved KxxKxxPRx amide structure widely identified in arthropods. While its involvement in the regulation of molting and reproduction in insects is well-established, its role in crustaceans has been overlooked. This study aimed to de-orphanise a receptor for ETH in the mud crab <em>Scylla paramamosain</em> and explore its potential impact on ovarian development. A 513-amino-acid G protein-coupled receptor for ETH (<em>Sp</em>ETHR) was identified in <em>S. paramamosain</em>, exhibiting a dose-dependent activation by <em>Sp</em>ETH with an EC<sub>50</sub> value of 75.18 nM. Tissue distribution analysis revealed <em>SpETH</em> was in the cerebral ganglion and thoracic ganglion, while <em>SpETHR</em> was specifically expressed in the ovary, hepatopancreas, and Y-organ of female crabs. <em>In vitro</em> experiments demonstrated that synthetic <em>Sp</em>ETH (at a concentration of 10<sup>−8</sup> M) significantly increased the expression of <em>SpVgR</em> in the ovary and induced ecdysone biosynthesis in the Y-organ. <em>In vivo</em> experiments showed a significant upregulation of <em>SpEcR</em> in the ovary and <em>Disembodied</em> and <em>Shadow</em> in the Y-organ after 12 h of <em>Sp</em>ETH injection. Furthermore, a 16-day administration of <em>Sp</em>ETH significantly increased 20E titers in hemolymph, gonadosomatic index (GSI) and oocyte size of <em>S. paramamosain.</em> In conclusion, our findings suggest that <em>Sp</em>ETH may play stimulatory roles in ovarian development and ecdysone biosynthesis by the Y-organ.</p></div>\",\"PeriodicalId\":2,\"journal\":{\"name\":\"ACS Applied Bio Materials\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2024-07-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Applied Bio Materials\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1095643324001193\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MATERIALS SCIENCE, BIOMATERIALS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1095643324001193","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
引用次数: 0
摘要
蜕皮诱导激素(ETH)是一种神经肽激素,其特征是在节肢动物中广泛发现的保守的 KxxKxxPRx 酰胺结构。它参与昆虫蜕皮和繁殖的调节作用已得到公认,但在甲壳类动物中的作用却一直被忽视。本研究旨在对泥蟹Scylla paramamosain中的ETH受体进行去卟啉化,并探索其对卵巢发育的潜在影响。研究发现,Spylla paramamosain体内存在一种513氨基酸的G蛋白偶联ETH受体(SpETHR),它被SpETH激活时表现出剂量依赖性,EC50值为75.18 nM。组织分布分析表明,SpETH存在于雌蟹的大脑神经节和胸神经节,而SpETHR则特异性地表达于雌蟹的卵巢、肝胰腺和Y器官。体外实验表明,合成的 SpETH(浓度为 10-8 M)能显著增加卵巢中 SpVgR 的表达,并诱导 Y 器官中蜕皮激素的生物合成。体内实验表明,注射 SpETH 12 小时后,卵巢和 Y 器官中的 SpEcR 和 Disembodied 和 Shadow 表达明显上调。此外,注射 SpETH 16 天后,血淋巴中的 20E 滴度、性腺指数(GSI)和巴拉莫萨蟾蜍的卵母细胞大小均明显增加。总之,我们的研究结果表明,SpETH可能对卵巢发育和Y器官的蜕皮激素生物合成起到刺激作用。
Identification of ETH receptor and its possible roles in the mud crab Scylla paramamosain
Ecdysis-triggering hormone (ETH) is a neuropeptide hormone characterized by a conserved KxxKxxPRx amide structure widely identified in arthropods. While its involvement in the regulation of molting and reproduction in insects is well-established, its role in crustaceans has been overlooked. This study aimed to de-orphanise a receptor for ETH in the mud crab Scylla paramamosain and explore its potential impact on ovarian development. A 513-amino-acid G protein-coupled receptor for ETH (SpETHR) was identified in S. paramamosain, exhibiting a dose-dependent activation by SpETH with an EC50 value of 75.18 nM. Tissue distribution analysis revealed SpETH was in the cerebral ganglion and thoracic ganglion, while SpETHR was specifically expressed in the ovary, hepatopancreas, and Y-organ of female crabs. In vitro experiments demonstrated that synthetic SpETH (at a concentration of 10−8 M) significantly increased the expression of SpVgR in the ovary and induced ecdysone biosynthesis in the Y-organ. In vivo experiments showed a significant upregulation of SpEcR in the ovary and Disembodied and Shadow in the Y-organ after 12 h of SpETH injection. Furthermore, a 16-day administration of SpETH significantly increased 20E titers in hemolymph, gonadosomatic index (GSI) and oocyte size of S. paramamosain. In conclusion, our findings suggest that SpETH may play stimulatory roles in ovarian development and ecdysone biosynthesis by the Y-organ.