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Ecdysteroids Regulate the Levels of Molt-Inhibiting Hormone (MIH) Expression in the Blue Crab Callinectes sapidus

机译:蜕皮类固醇调节蓝蟹Callinectes sapidus中的蜕皮抑制激素(MIH)表达水平

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摘要

Arthropod molt is coordinated through the interplay between ecdysteroids and neuropeptide hormones. In crustaceans, changes in the activity of Y-organs during the molt cycle have been regulated by molt-inhibiting hormone (MIH) and crustacean hyperglycemic hormone (CHH). Little has been known of the mode of direct effects of ecdysteroids on the levels of MIH and CHH in the eyestalk ganglia during the molt cycle. This study focused on a putative feedback of ecdysteroids on the expression levels of MIH transcripts using in vitro incubation study with ecdysteroids and in vivo RNAi in the blue crab, Callinectes sapidus. Our results show a specific expression of ecdysone receptor (EcR) in which EcR1 is the major isoform in eyestalk ganglia. The initial elevation of MIH expression at the early premolt stages is replicated by in vitro incubations of eyestalk ganglia with ecdysteroids that mimic the intrinsic conditions of D0 stage: the concentration (75 ng/ml) and composition (ponasterone A and 20-hydroxyecdysone at a 3:1 (w:w) ratio). Additionally, multiple injections of EcR1-dsRNA reduce MIH expression by 67%, compared to the controls. Our data provide evidence on a putative feedback mechanism of hormonal regulation during molting cycle, specifically how the molt cycle is repeated during the life cycle of crustaceans. The elevated concentrations of ecdysteroids at early premolt stage may act positively on the levels of MIH expression in the eyestalk ganglia. Subsequently, the increased MIH titers in the hemolymph at postmolt would inhibit the synthesis and release of ecdysteroids by Y-organs, resulting in re-setting the subsequent molt cycle.
机译:节肢动物蜕皮是通过蜕皮类固醇和神经肽激素之间的相互作用来协调的。在甲壳类动物中,蜕皮周期中Y器官活性的变化已由蜕皮抑制激素(MIH)和甲壳类高血糖激素(CHH)调节。蜕皮类固醇对蜕皮周期中眼球神经节中MIH和CHH的直接作用方式知之甚少。这项研究集中在蜕皮类固醇对MIH转录物表达水平的推定反馈上,该研究利用蜕皮类固醇和体内RNAi在蓝蟹Callinectes sapidus中进行的体外温育研究。我们的结果显示了蜕皮激素受体(EcR)的特定表达,其中EcR1是眼球神经节中的主要同工型。在蜕皮前期早期,MIH表达的最初升高是通过将模仿E0内在条件的蜕皮类固醇在体外孵育眼轴神经节来复制的:浓度(75 ng / ml)和组成(桥骨酮A和20-羟基蜕皮酮在3:1(w:w)的比例)。此外,与对照组相比,多次注射EcR1-dsRNA可使MIH表达降低67%。我们的数据提供了蜕皮周期中激素调节的推定反馈机制的证据,特别是在甲壳动物的生命周期中蜕皮周期如何重复。蜕皮前期蜕皮类固醇的浓度升高可能对眼球神经节中MIH的表达有积极作用。随后,蜕皮后血淋巴中MIH滴度的增加会抑制Y器官对蜕皮类固醇的合成和释放,从而导致随后的蜕皮周期重新设定。

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    Sirinart Techa; J. Sook Chung;

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  • 年(卷),期 -1(10),4
  • 年度 -1
  • 页码 e0117278
  • 总页数 19
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