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氯化汞诱导鸡脾脏淋巴细胞中硒蛋白的异常基因表达。

Aberrant Gene Expression of Selenoproteins in Chicken Spleen Lymphocytes Induced by Mercuric Chloride.

作者信息

Chu Jia-Hong, Yan Yu-Xue, Chen Xue-Wei, Gao Pei-Chao, Li Lan-Xin, Fan Rui-Feng

机构信息

College of Animal Science and Veterinary Medicine, Shandong Agricultural University, 61 Daizong Street, Tai'an City, 271018, Shandong Province, China.

Shandong Provincial Key Laboratory of Animal Biotechnology and Disease Control and Prevention, Shandong Agricultural University, 61 Daizong Street, Tai'an City, 271018, Shandong Province, China.

出版信息

Biol Trace Elem Res. 2022 Jun;200(6):2857-2865. doi: 10.1007/s12011-021-02870-4. Epub 2021 Aug 26.

Abstract

Mercury (Hg) is a heavy metal widely distributed in ecological environment, poisoning the immune system of humans and animals. Selenium (Se) is an essential microelement and selenoproteins involved in the procedure of Se antagonizing organ toxicity induced by heavy metals. The aim of this research was to investigate the changes of gene expression profile of selenoproteins induced by mercuric chloride (HgCl) in chicken spleen lymphocytes. We established cytotoxicity model of chicken spleen lymphocytes by HgCl exposure, the messenger RNA (mRNA) expression levels of 25 selenoproteins in spleen lymphocytes were analyzed by real-time quantitative PCR (qPCR), and the gene expression pattern of selenoproteins was revealed by principal component analysis (PCA). The results showed that the mRNA expression levels of 13 selenoproteins (GPX3, GPX4, TXNRD2, TXNRD3, DIO2, SELENOS, SELENON, SELENOT, SELENOO, SELENOP, SELENOP2, MSRB1, and SEPHS2) were decreased in HgCl treatment group, and there was strong positive correlation between these selenoproteins and component 1 as well as component 2 of the PCA. At the same time, the protein expression levels of GPX4, TXNRD1, TXNRD2, SELENOM, SELENOS, and SELENON were detected by Western blotting, which were consistent with the changes of gene expression. The results showed that the expression levels of selenoproteins were aberrant in response to HgCl toxicity. The information presented in this study provided clues for further research on the interaction between HgCl and selenoproteins, and the possible mechanism of immune organ toxicity induced by HgCl.

摘要

汞(Hg)是一种广泛分布于生态环境中的重金属,会毒害人类和动物的免疫系统。硒(Se)是一种必需的微量元素,硒蛋白参与了硒拮抗重金属诱导的器官毒性的过程。本研究的目的是探讨氯化汞(HgCl)诱导鸡脾脏淋巴细胞中硒蛋白基因表达谱的变化。我们通过HgCl暴露建立了鸡脾脏淋巴细胞的细胞毒性模型,采用实时定量PCR(qPCR)分析脾脏淋巴细胞中25种硒蛋白的信使核糖核酸(mRNA)表达水平,并通过主成分分析(PCA)揭示硒蛋白的基因表达模式。结果显示,HgCl处理组中13种硒蛋白(GPX3、GPX4、TXNRD2、TXNRD3、DIO2、SELENOS、SELENON、SELENOT、SELENOO、SELENOP、SELENOP2、MSRB1和SEPHS2)的mRNA表达水平降低,这些硒蛋白与PCA的成分1和成分2之间存在强正相关。同时,通过蛋白质免疫印迹法检测了GPX4、TXNRD1、TXNRD2、SELENOM、SELENOS和SELENON的蛋白表达水平,其与基因表达变化一致。结果表明,硒蛋白的表达水平在HgCl毒性作用下出现异常。本研究提供的信息为进一步研究HgCl与硒蛋白之间的相互作用以及HgCl诱导免疫器官毒性的可能机制提供了线索。

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