Abhipsha Dey , Rigolin Nayak , Martin Prchal , Alvaro Gonzalez-Cid , Martin Pšenička , Radek Šindelka , Martin Flajšhans , Ievgeniia Gazo
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引用次数: 0
摘要
胚胎中的 DNA 损伤会影响生物体的发育。了解鱼类物种不同生命阶段的差异对于生态风险评估措施至关重要。我们对两种非模型鱼类--乌塘鳢和鲤鱼--的DNA损伤敏感性进行了研究。这些鱼类的胚胎在卵裂(2 细胞)期和胚胎发育期暴露于模式基因毒性物质喜树碱(CPT)。结果表明,只有在卵裂阶段才会出现物种特异性的DNA损伤敏感性。3nM CPT 会导致赤子鱼胚胎死亡,而鲤鱼胚胎则能正常孵化。在胃早期阶段,可观察到立体小鱼胚胎出现多种核异常。然而,只有在暴露于 7nM CPT 时,鲤鱼胚胎才会在神经期出现核异常和 DNA 断裂。此外,鲤鱼胚胎中 tp53 的表达量在胃肠期有所增加,这表明鲤鱼胚胎启动了细胞凋亡机制。这些研究结果表明,在相同的发育阶段,鲤鱼胚胎激活 DNA 损伤反应的效率要高于甲鱼胚胎。
Species-specific differences in DNA damage sensitivity at early developmental stage: A comparative study of sterlet (Acipenser ruthenus) and common carp (Cyprinus carpio)
DNA damage in embryos shapes the development of an organism. Understanding life stage-specific differences between fish species is essential for ecological risk assessment measures. We explored DNA damage sensitivity in two nonmodel fish species, sterlet (Acipenser ruthenus) and common carp (Cyprinus carpio). Embryos of these species were exposed to a model genotoxicant, camptothecin (CPT), during cleavage (2-cell) stage and gastrulation. Results revealed a species-specific DNA damage sensitivity only at cleavage stage. 3 nM CPT caused lethality in sterlet embryos while carp embryos hatched normally. Multiple nuclear abnormalities were observed in sterlet embryos by early gastrula stage. However, carp embryos exhibited nuclear abnormalities and DNA fragmentation at neurula stage only when exposed to 7 nM CPT. Moreover, increased expression of tp53 in carp embryos at gastrula stage suggests activation of apoptosis mechanism. These findings suggest that carp embryos activate DNA damage response more efficiently than sterlet embryos at same developmental stage.
期刊介绍:
Environmental Toxicology and Pharmacology publishes the results of studies concerning toxic and pharmacological effects of (human and veterinary) drugs and of environmental contaminants in animals and man.
Areas of special interest are: molecular mechanisms of toxicity, biotransformation and toxicokinetics (including toxicokinetic modelling), molecular, biochemical and physiological mechanisms explaining differences in sensitivity between species and individuals, the characterisation of pathophysiological models and mechanisms involved in the development of effects and the identification of biological markers that can be used to study exposure and effects in man and animals.
In addition to full length papers, short communications, full-length reviews and mini-reviews, Environmental Toxicology and Pharmacology will publish in depth assessments of special problem areas. The latter publications may exceed the length of a full length paper three to fourfold. A basic requirement is that the assessments are made under the auspices of international groups of leading experts in the fields concerned. The information examined may either consist of data that were already published, or of new data that were obtained within the framework of collaborative research programmes. Provision is also made for the acceptance of minireviews on (classes of) compounds, toxicities or mechanisms, debating recent advances in rapidly developing fields that fall within the scope of the journal.