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土壤无脊椎动物胚胎中的高通量基因表达 - 穴居环节动物对镉毒性的作用机制。

High-throughput gene expression in soil invertebrate embryos - Mechanisms of Cd toxicity in Enchytraeus crypticus.

机构信息

Department of Biology & CESAM, University of Aveiro, 3810-193, Aveiro, Portugal.

Department of Biology & CESAM, University of Aveiro, 3810-193, Aveiro, Portugal.

出版信息

Chemosphere. 2018 Dec;212:87-94. doi: 10.1016/j.chemosphere.2018.08.068. Epub 2018 Aug 15.

DOI:10.1016/j.chemosphere.2018.08.068
PMID:30142569
Abstract

Gene expression can vary with the organisms' life stage. It is known that embryos can be more sensitive to toxicant exposure, as previously demonstrated for Enchytraeus crypticus (Oligochaeta) exposed to cadmium (Cd), known to cause embryotoxicity and hatching delay. It was shown that Ca enters embryos via the L-type Ca channels in the cocoon membrane, this being affected in Cd exposed embryos (Cd-Ca competition is well-known). In the present study, the embryotoxic mechanisms of Cd were studied via high-throughput gene expression for E. crypticus. Cocoons (1-2 days old), instead of the adult organism, were exposed in Cd spiked LUFA 2.2 soil during 1 day. Results showed that Cd affected Ca homeostasis which is implicated in several other molecular processes. Several of the major modulators of Cd toxicity (e.g., impaired gene expression, cell cycle arrest, DNA and mitochondrial damage) were identified in the embryos showing its relevancy as a model in ecotoxicogenomics. The draft Adverse Outcome Pathway was improved. Previously was hypothesized that gene regulation mechanisms were activated to synthesize more Ca channel proteins - this was confirmed here. Further, novel evidences were that, besides the extracellular competition, Cd competes intracellularly which causes a reduction in Ca efflux, and potentiates Cd embryotoxicity.

摘要

基因表达会随生物体的生命阶段而变化。众所周知,胚胎对毒物暴露更为敏感,此前在暴露于镉(Cd)的真涡虫(Oligochaeta)中得到了证实,镉已知会导致胚胎毒性和孵化延迟。研究表明,Ca 通过茧膜中的 L 型 Ca 通道进入胚胎,而暴露于 Cd 的胚胎中的这种通道会受到影响(Cd-Ca 竞争是众所周知的)。在本研究中,通过真涡虫的高通量基因表达研究了 Cd 的胚胎毒性机制。在 LUFA 2.2 土壤中添加 Cd 后,将 1-2 天大的茧(而不是成年生物体)暴露于其中 1 天。结果表明,Cd 影响 Ca 稳态,而 Ca 稳态与其他几个分子过程有关。在表现出相关性的胚胎中鉴定出了 Cd 毒性的几种主要调节剂(例如,基因表达受损、细胞周期停滞、DNA 和线粒体损伤),这表明它作为生态毒理学基因组学的模型具有重要意义。不良结局途径草案得到了改进。此前假设基因调控机制被激活以合成更多的 Ca 通道蛋白——这在此得到了证实。此外,新的证据表明,除了细胞外竞争外,Cd 还在细胞内竞争,这导致 Ca 外排减少,并增强了 Cd 的胚胎毒性。

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