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体外蛋白质沉淀作为化学诱导细胞毒性的一种检测方法:EDIT子程序。

Protein precipitation In Vitro as a measure of chemical-induced cytotoxicity: an EDIT sub-programme.

作者信息

Novillo A, Ekwall B, Castaño A

机构信息

Environmental Toxicology, CISA-INIA, Valdeolmos 28130, Madrid, Spain.

出版信息

Altern Lab Anim. 2001 May-Jun;29(3):309-24. doi: 10.1177/026119290102900315.

Abstract

As a priority area of the Evaluation-Guided Development of In Vitro Toxicity and Toxicokinetic Tests (EDIT) programme, an in vitro protein precipitation (PP) assay was used on the 50 reference chemicals of the Multicentre Evaluation of In Vitro Cytotoxicity (MEIC) project, to confirm and extend the MEIC results. Dose-response curves were generated for only 30 of the chemicals, and the concentrations causing 10% (EC10) and 50% (EC50) protein precipitation versus the positive control were chosen as endpoints. The number of chemicals with a positive response increased to 46 when a new endpoint, the minimum effect concentration (MEC) that induces protein precipitation with respect to the negative control, was used. When the results were correlated with in vitro cytotoxicity in human cell lines, a similarly good correlation was found between the various endpoints of the PP assay at 5 hours and the 24-hour IC50 average cytotoxicity in human cell lines, even though the number of chemicals included in the correlation was larger for the MEC. Using the prediction error, the endpoint that gave the best correlation between the PP assay and human cell cytotoxicity was once more found to be the 5-hour MEC, and this was chosen for the PP assay. The sensitivity of the PP assay is lower than that of the in vitro cell-line cytotoxicity assay, possibly due to its shorter exposure period and because precipitation is the ultimate event in the sequence of a protein disturbance. It is expected that earlier denaturation steps would give better sensitivity. However, this simple, inexpensive and rapid assay could be useful in the early stages of testing chemicals.

摘要

作为体外毒性和毒代动力学试验评估导向开发(EDIT)项目的一个优先领域,体外蛋白质沉淀(PP)试验被用于多中心体外细胞毒性评估(MEIC)项目的50种参考化学物质,以确认并扩展MEIC的结果。仅为其中30种化学物质生成了剂量-反应曲线,并选择相对于阳性对照引起10%(EC10)和50%(EC50)蛋白质沉淀的浓度作为终点。当使用一个新的终点,即相对于阴性对照诱导蛋白质沉淀的最小效应浓度(MEC)时,出现阳性反应的化学物质数量增加到46种。当将结果与人类细胞系中的体外细胞毒性相关联时,尽管用于关联分析的化学物质数量对于MEC更多,但在PP试验的不同终点与人类细胞系中24小时IC50平均细胞毒性之间仍发现了同样良好的相关性。使用预测误差,再次发现PP试验与人类细胞毒性之间相关性最佳的终点是5小时MEC,因此将其选作PP试验的终点。PP试验的灵敏度低于体外细胞系细胞毒性试验,这可能是由于其暴露时间较短,且沉淀是蛋白质干扰序列中的最终事件。预计更早的变性步骤会有更好的灵敏度。然而,这种简单、廉价且快速的试验在化学物质测试的早期阶段可能会有用。

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