Markers of combined aerogenic exposure to metal oxides and transformed plasma proteomic profiles in children

M. Zemlyanova, N. Zaitseva, Yu. V. Koldibekova, E. V. Peskova, N. Bulatova, M. Stepankov
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Abstract

Changes in homeostatic balance of the body, primarily at the cellular-molecular level, are a relevant research object in fundamental and applied studies. They can be eligible indicators for predicting negative effects under exposure to chemical risk factors. The aim of this study was to substantiate markers of a transformed plasma proteomic profile in children. These markers should have prognostic value and an evidence-based association with combined aerogenic exposure to metal oxides (copper and nickel oxides used as an example). We propose an innovative methodical approach based on plasma proteomic profiling that includes the following: identification of identical proteins and genes encoding their expression; quantification of indicators within the ‘identical protein – a chemical concentration in blood’ system; prediction of negative effects as per indicators of homeostasis destabilization at the cellular-molecular level under chronic aerogenic exposure to chemicals. The proposed algorithm was tested by comparing changed proteins and peptides identified in plasma proteomic profiles of children exposed simultaneously to nickel and copper oxides in ambient air in actual conditions and small rodents under experimental combined and isolated exposure to the analyzed chemicals in levels equal to real ones. Long-term aerogenic exposure simultaneously to copper and nickel oxides was established to create elevated nickel and copper levels in blood of exposed children substantiated as markers of exposure. They were up to 2.4 times higher against the same indicators in unexposed children and reference levels as well. The results of field observations were verified by elevated levels of the same chemicals in blood under experimental modelling of an equivalent combined exposure performed on biological models. APOBEC1 complement factor (the А1CF gene) was substantiated as an identical proteomic marker based on plasma proteomic profiling in experimental and field investigations. It has an evidence-based association with markers of exposure (nickel and copper simultaneously identified in blood). Lower expression of this protein under persistent combined aerogenic exposure to nickel and copper oxides makes it possible to predict such a negative effect as modification of low density lipoproteins with further induction of atherosclerotic changes in vessels, the latter being a risk factor of cardiovascular diseases.
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儿童联合空气源暴露于金属氧化物和转化血浆蛋白质组谱的标志物
体内稳态平衡的变化,主要是在细胞-分子水平上的变化,是基础研究和应用研究的相关研究对象。它们可以作为预测暴露于化学品危险因素下的负面影响的合格指标。本研究的目的是证实儿童转化血浆蛋白质组谱的标记物。这些标志物应具有预后价值,并与金属氧化物(以铜和镍氧化物为例)的联合气源暴露有循证关联。我们提出了一种基于血浆蛋白质组学分析的创新方法,包括以下内容:鉴定相同的蛋白质和编码其表达的基因;“相同蛋白质-血液中的化学浓度”系统内指标的量化;慢性气体化学物质暴露下,根据细胞分子水平稳态不稳定指标的负面影响预测。通过比较在实际条件下同时暴露于环境空气中镍和铜氧化物的儿童和实验组合和孤立暴露于与实际水平相等的分析化学物质的小型啮齿动物的血浆蛋白质组学谱中发现的变化的蛋白质和肽,对所提出的算法进行了测试。长期空气源性同时暴露于铜和镍氧化物中,可使暴露儿童血液中的镍和铜水平升高,并证实这是暴露的标志。与未接触的儿童的相同指标和参考水平相比,它们高出2.4倍。在对生物模型进行等效联合接触的实验模拟下,通过血液中相同化学物质水平的升高证实了实地观察的结果。APOBEC1补体因子(А1CF基因)是一种基于血浆蛋白质组学分析的相同蛋白质组学标记。它与暴露标志物(在血液中同时发现镍和铜)有证据关联。在镍和铜氧化物的持续联合气源暴露下,该蛋白的低表达使得可以预测低密度脂蛋白的修饰等负面影响,从而进一步诱导血管动脉粥样硬化变化,后者是心血管疾病的一个危险因素。
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来源期刊
Health Risk Analysis
Health Risk Analysis Medicine-Health Policy
CiteScore
1.30
自引率
0.00%
发文量
38
审稿时长
20 weeks
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