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Caenorhabditis elegans Metallothioneins Protect against Toxicity Induced by Depleted Uranium

机译:秀丽隐杆线虫金属硫蛋白可防止贫铀引起的毒性

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Depleted uranium (DU) is a dense and heavy metal used in armor, ammunition, radiation shielding, and counterbalances. The military usage has led to growing public concern regarding the health effects of DU. In this study, we used the nematode, Caenorhabditis elegans, to evaluate the toxicity of DU and its effects in knockout strains of metallothioneins (MTs), which are small thiol-rich proteins that have numerous functions, such as metal sequestration, transport, and detoxification. We examined nematode viability, the accumulation of uranium, changes in MT gene expression by quantitative reverse transcription-PCR, and the induction of green fluorescent protein under the control of the MT promoters, following exposure to DU. Our results indicate that (1) DU causes toxicity in a dose-dependent manner; (2) MTs are protective against DU exposure; and (3) nematode death by DU is not solely a reflection of intracellular uranium concentration. (4) Furthermore, only one of the isoforms of MTs, metallothionein-1 (mtl-1), appears to be important for uranium accumulation in C. elegans. These findings suggest that these highly homologous proteins may have subtle functional differences and indicate that MTs mediate the response to DU.
机译:贫铀(DU)是一种重金属,用于装甲,弹药,辐射屏蔽和制衡。军事用途已引起公众对DU的健康影响的日益关注。在这项研究中,我们使用线虫秀丽隐杆线虫(Caenorhabditis elegans)来评估DU的毒性及其对敲除金属硫蛋白(MTs)菌株的作用,这些金属硫蛋白是富含硫醇的小蛋白,具有多种功能,例如金属螯合,转运和转运排毒。我们研究了线虫的生存能力,铀的积累,通过定量逆转录PCR进行MT基因表达的变化以及暴露于DU后在MT启动子控制下诱导绿色荧光蛋白的过程。我们的结果表明:(1)DU以剂量依赖性方式引起毒性; (2)MT可防止DU暴露; (3)DU引起的线虫死亡不仅仅反映细胞内铀浓度。 (4)此外,MT的同工型中只有一种,金属硫蛋白-1(mtl-1),对于秀丽隐杆线虫中的铀积累似乎很重要。这些发现表明这些高度同源的蛋白质可能具有细微的功能差异,并表明MT介导了对DU的应答。

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  • 来源
    《Toxicological Sciences》 |2009年第2期|p.345-354|共10页
  • 作者单位

    *Department of Pediatrics, Vanderbilt University Medical Center, Nashville, Tennessee 37232 †Pharmaceutical Sciences Division, School of Biomedical &

    Health Sciences, King’s College London, London, UK ‡Department of Neuroscience, Faculty of Medicine, Norwegian University of Science and Technology, Trondheim, Norway §Kennedy Center for Research on Human Development, Vanderbilt University Medical Center, Nashville, Tennessee 37232;

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