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Development of an in vitro photosafety evaluation method utilizing intracellular ROS production in THP-1 cells

机译:在THP-1细胞中使用细胞内ROS产生的体外光度评价方法的研制

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Photoreactive compounds that may experience exposure to ultraviolet (UV) radiation can lead to the intracellular production of reactive oxygen species (ROS), which may cause phototoxic and photoallergenic responses. Here, we developed a novel in vitro photosafety assay and investigated whether it could be used to predict phototoxicity and photosensitivity by measuring changes in intracellular ROS production. THP-1 cells that had previously taken up 5-(and-6)-carboxy-2',7'-difluorodihydrofluorescein diacetate (carboxy-H(2)DFFDA), a ROS-sensitive fluorescent reagent, were exposed to photoreactive substances such as phototoxic and photoallergenic materials and then subjected to with UV-A irradiation (5 J/cm(2)). The fluorescence intensity was subsequently measured using a flow cytometer, and the intracellular ROS production was calculated. A statistically significant increase in ROS following treatment with photoreactive substances was observed in cells irradiated with UV-A. In contrast, no significant increase was observed for non-photoreactive substances in comparison to the control solution. Next, to confirm the impact of intracellular ROS on the photosensitive response, changes in CD86 and CD54 expression were measured following quencher addition during the photo human cell line activation test (photo h-CLAT). The results confirmed the reduction of CD86 and CD54 expression in response to photoallergenic substances following quencher addition. Together, these findings suggest that intracellular ROS production is involved in photosensitizing reactions. Therefore, we suggest that the developed method utilizing intracellular ROS production as an index may be useful as a novel in vitro evaluation tool for photoreactive substances.
机译:可能经历暴露于紫外线(UV)辐射的光反应性化合物可导致对反应性氧物质(ROS)的细胞内产生,这可能导致光毒性和光子收缩响应。在这里,我们开发了一种新的体外照片安全测定,并研究了它是否可用于通过测量细胞内ROS生产的变化来预测光毒性和光敏性。先前占用5-(和-6)-carboxy-2',7'-二氟致氢荧光荧光素二乙酸酯(羧基-H(2)DFFDA),ROS敏感荧光试剂,暴露于光反应性物质的THP-1细胞作为光毒性和光晶体材料,然后用UV-A辐射(5J / cm(2))进行。随后使用流式细胞仪测量荧光强度,并计算细胞内ROS产生。在用UV-A照射的细胞中观察到使用光反应物质处理后ROS的统计学显着增加。相反,与对照溶液相比,对非光反应性物质没有观察到显着增加。接下来,为了确认细胞内RO对感光响应的影响,在光学人细胞系活化试验(Photo H-Clat)期间猝灭剂添加后测定CD86和CD54表达的变化。结果证实了CD86和CD54表达的减少,响应猝灭剂添加后的光晶体物质。这些发现表明,细胞内ROS生产参与了光敏反应。因此,我们建议利用细胞内ROS生产作为指数的开发方法可用作用于光反应性物质的新型体外评估工具。

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