Responses of lipid metabolism in Rana chensinensis tadpoles under lead (Pb) stress

IF 2.2 2区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Xiaoli Liu , Ying Liu , Xiuling Song , Hongyuan Wang , Lihong Chai
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Abstract

Lead (Pb) is a toxic contaminant ubiquitously present in aquatic ecosystems. Unfortunately, studies on the effects of Pb on lipid metabolism and gene expression in amphibians are limited. Here, lipidomic and hepatic transcriptomic analyses were performed on Rana chensinensis tadpoles exposed to 20 and 200 μg/L Pb. Our data demonstrated that phosphatidylcholine (PC) species were significantly reduced in the Pb20 group and significantly increased in the Pb200 group. The decrease in PC content may be related to membrane damage in tadpoles. Meanwhile, liver transcriptome profiling revealed that differentially expressed genes induced by different concentrations of Pb treatment were simultaneously enriched in Staphylococcus aureus infection pathway, with significantly increased expression of FB, C3, and MHC-II in the Pb20 group and C3AR1 in the Pb200 group. Moreover, Pb exposure resulted in liver damage (e.g., lipid droplet accumulation) and significantly reduced body size in tadpoles at metamorphosis, which may have increased their susceptibility to mortality. This study is the first to investigate the deleterious effects of Pb on lipid metabolism and hepatic gene expression in tadpoles, shedding light on the potential molecular mechanisms of Pb toxicity in amphibians.

Abstract Image

铅胁迫下中国林蛙蝌蚪脂质代谢的响应
铅(Pb)是水生生态系统中普遍存在的有毒污染物。不幸的是,关于铅对两栖动物脂质代谢和基因表达影响的研究有限。本研究对暴露于20和200 μg/L Pb的中国林蛙蝌蚪进行了脂质组学和肝脏转录组学分析。我们的数据表明,磷脂酰胆碱(PC)物种在Pb20组显著减少,在Pb200组显著增加。PC含量的降低可能与蝌蚪膜损伤有关。同时,肝脏转录组分析显示,不同浓度Pb处理诱导的差异表达基因在金黄色葡萄球菌感染途径中同时富集,Pb20组中FB、C3和MHC-II的表达显著增加,Pb200组中C3AR1的表达显著增加。此外,铅暴露导致蝌蚪蜕变期肝脏损伤(如脂滴积聚)和体型显著减小,这可能增加了蝌蚪的死亡率。本研究首次研究了铅对蝌蚪脂质代谢和肝脏基因表达的有害影响,揭示了铅对两栖动物毒性的潜在分子机制。
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来源期刊
CiteScore
5.10
自引率
3.30%
发文量
69
审稿时长
33 days
期刊介绍: Comparative Biochemistry & Physiology (CBP) publishes papers in comparative, environmental and evolutionary physiology. Part D: Genomics and Proteomics (CBPD), focuses on “omics” approaches to physiology, including comparative and functional genomics, metagenomics, transcriptomics, proteomics, metabolomics, and lipidomics. Most studies employ “omics” and/or system biology to test specific hypotheses about molecular and biochemical mechanisms underlying physiological responses to the environment. We encourage papers that address fundamental questions in comparative physiology and biochemistry rather than studies with a focus that is purely technical, methodological or descriptive in nature.
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