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Exposure to particle debris generated from passenger and truck tires induces different genotoxicity and inflammatory responses in the RAW 264.7 cell line

机译:暴露于乘客轮胎和卡车轮胎产生的颗粒碎片会在RAW 264.7细胞系中诱导不同的遗传毒性和炎症反应

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摘要

A number of studies have shown variable grades of cytotoxicity and genotoxicity in in vitro cell cultures, laboratory animals and humans when directly exposed to particle debris generated from tires. However, no study has compared the effects of particles generated from passenger tires with the effects of particles from truck tires. The aim of this study was to investigate and relate the cyto- and genotoxic effects of different types of particles (PP, passenger tire particles vs. TP, truck tire particles) in vitro using the phagocytic cell line RAW 264.7 (mouse leukaemic monocyte macrophage cell line). The viability of RAW 264.7 cells was determined by the 3- (4,5-dimethylthiazol-2-yl) -5- (3-carboxymethoxyphenyl) -2- (4-sulfophenyl) -2H-tetrazolium (MTS) assay following exposure for 4, 24 and 48 hours to different particle concentrations (10 μg / ml, 25 μg / ml, 50 μg / ml, 100 μg / ml). The effects of particles of passenger and truck tires on cell proliferation and genotoxicity were evaluated by means of the cytokinesis-block micronucleus (CBMN) assay following exposure for 24 hours to different particle concentrations (10 μg / ml, 25 μg / ml, 50 μg / ml, 100 μg / ml). In MTS assay, after 24 hours, it was found that PP induced a 30% decrease in metabolic activity at a concentration of 10 μg/ml, while TP caused reductions of 20% and 10% at concentrations of 10 μg/ml and 50 μg/ml, respectively. At 48 hours after the treatments, we observed increased metabolic activity at 50 μg/ml and 100 μg/ml for the PP while only at 50 μg/ml for the TP. The CBMN assay showed a significant increase in the number of micronuclei in the cells incubated with PP in all experimental conditions, while the cells treated with TP showed a meaningful increase only at 10 μg /ml. We utilized the TNF-α ELISA mouse test to detect the production of tumour necrosis factor-alpha (TNF-α) in RAW 264.7 cells. The effect of passenger and truck particles on TNF-α release was evaluated following exposure for 4 and 24 hours.After 4 hours of incubation, the cells treated with PP and TP at 100 μg / ml showed a slight but significant increase in TNF-α release, while there was a significant increase in the release of TNF-α after 24 hours of incubation with both tire samples in the cells treated with 50 and 100 μg / ml PP. The data obtained show a higher cytotoxic, clastogenic/genotoxic and inflammatory effects of passenger compared to the truck tire particles.
机译:大量研究表明,当直接暴露于轮胎产生的碎屑时,在体外细胞培养,实验动物和人类中,细胞毒性和遗传毒性的等级不同。然而,没有研究将乘用轮胎产生的颗粒的影响与卡车轮胎产生的颗粒的影响进行比较。这项研究的目的是使用吞噬细胞系RAW 264.7(小鼠白血病单核巨噬细胞)研究并关联不同类型颗粒(PP,乘用轮胎颗粒与TP,卡车轮胎颗粒)的细胞毒性和遗传毒性作用。线)。暴露后暴露于3-(4,5-二甲基噻唑-2-基)-5-(3-羧基甲氧基苯基)-2-(4-磺基苯基)-2H-四唑鎓(MTS),测定RAW 264.7细胞的活力。在4、24和48小时内达到不同的颗粒浓度(10μg/ ml,25μg/ ml,50μg/ ml,100μg/ ml)。暴露于不同的颗粒浓度(10μg/ ml,25μg/ ml,50μg)24小时后,通过胞质分裂阻滞微核(CBMN)测定法评估了客运和卡车轮胎颗粒对细胞增殖和遗传毒性的影响。 / ml,100μg/ ml)。在MTS分析中,发现24小时后,PP在10μg/ ml的浓度下会引起30%的代谢活性降低,而TP在10μg/ ml和50μg的浓度下会引起20%和10%的降低。 / ml。在治疗后48小时,我们观察到PP的代谢活性增加到50μg/ ml和100μg/ ml,而TP仅增加了50μg/ ml。 CBMN分析显示,在所有实验条件下,与PP孵育的细胞中微核数量均显着增加,而TP处理的细胞仅在10μg/ ml时才显示出有意义的增加。我们利用TNF-αELISA小鼠测试来检测RAW 264.7细胞中肿瘤坏死因子-α(TNF-α)的产生。暴露4和24小时后评估乘客和卡车颗粒对TNF-α释放的影响。孵育4小时后,以100μg/ ml的PP和TP处理的细胞显示TNF-α略有但显着增加在用50和100μg/ ml PP处理的细胞中,两种轮胎样品孵育24小时后,TNF-α的释放均显着增加。所获得的数据显示,与卡车轮胎颗粒相比,乘客具有更高的细胞毒,杀伤/遗传和炎症作用。

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