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首页> 外文期刊>Biochimica et biophysica acta. Molecular cell research >Volatile organic compounds cytotoxicity and expression of HSP72, HSP90 and GRP78 stress proteins in cultured human cells
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Volatile organic compounds cytotoxicity and expression of HSP72, HSP90 and GRP78 stress proteins in cultured human cells

机译:挥发性有机化合物在培养的人细胞中的细胞毒性和HSP72,HSP90和GRP78应激蛋白的表达

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摘要

The aim of this study was to determine whether overexpression of stress proteins (SPs) could be a sensitive biomarker for cell injury due to exposure to low doses of volatile organic compounds (VOCs) such as benzene, ethylbenzene, toluene, xylene, and chlorinated derivatives (CiB). Sublethal and cytotoxic threshold concentrations of the VOCs were determined by studying the growth rate of normal (fibroblasts) or tumor-derived human cell lines (A549, HepG2) exposed for 4 days to VOCs. Changes in SP expression as a function of concentrations were investigated by Western blotting. VOC toxicity was found to be correlated with their degree of chlorination and their hydrophobicity. Cytotoxic threshold concentrations (no-observed effect concentration, NOEC) were found to be similar for the three cell lines. It was observed that using a mixture of VOCs, each of them at concentration below the NOEC, resulted in an actual toxicity to the cells. This finding reveals a synergistic effect and should by taken into account when assessing threshold risk and exposure limit values in the worker's environment when several pollutants may be present. HSP72 and HSP90 expression levels were not affected whereas GRP78 expression was increased by all the VOCs. Taking into account the specific molecular function of GRP78, it suggests that VOC exposure results in misfolded or underglycosylated protein accumulation in the endoplasmic reticulum. GRP78 overexpression was closely related to the magnitude of growth inhibition due to increasing concentrations of each VOC. The overexpression was found to be significant for concentrations 5 to 30 times higher than NOEC, indicating that, under our experimental conditions, GRP78 expression cannot be considered as a sensitive biomarker of exposure to environmental VOCs.
机译:这项研究的目的是确定是否由于暴露于低剂量的挥发性有机化合物(VOC)(如苯,乙苯,甲苯,二甲苯和氯化衍生物)而导致应激蛋白(SP)的过度表达成为细胞损伤的敏感生物标志物。 (CiB)。通过研究暴露于VOC 4天的正常(成纤维细胞)或肿瘤来源的人类细胞系(A549,HepG2)的生长速率,确定VOC的亚致死浓度和细胞毒性阈值浓度。通过蛋白质印迹研究SP表达随浓度的变化。发现VOC毒性与其氯化程度和疏水性有关。发现三种细胞系的细胞毒性阈值浓度(未观察到的作用浓度,NOEC)相似。观察到,使用VOC的混合物(每种浓度低于NOEC)会导致对细胞的实际毒性。该发现揭示了协同效应,当评估可能存在多种污染物的工人环境中的阈值风险和暴露极限值时,应予以考虑。 HSP72和HSP90的表达水平不受影响,而所有VOC均增加了GRP78的表达。考虑到GRP78的特定分子功能,这表明VOC暴露会导致内质网中折叠错误或糖基化不足的蛋白质积聚。由于每种VOC浓度的增加,GRP78的过表达与生长抑制的幅度密切相关。发现过表达对于浓度比NOEC高5至30倍是显着的,表明在我们的实验条件下,GRP78表达不能被视为暴露于环境VOC的敏感生物标志物。

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