New methods for cytotoxicity testing: quantitative video microscopy of intracellular motion and mitochondria-specific fluorescence.

Molecular toxicology Pub Date : 1987-09-01
W Maile, T Lindl, D G Weiss
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Abstract

The aim of this study is to qualify the application the new microscopic methods fluorescence and AVEC-DIC (Allen video-enhanced contrast differential interference contrast) microscopy for toxicity testing. The effects of 2-OH-ethyl methacrylate (HEMA), a toxic acrylic monomer, on human fibroblasts was tested. The HEMA concentrations used were 0.01-1% at incubation times of 1-24 h. The cells were observed with AVEC-DIC microscopy and fluorescent staining to evaluate the velocity of lysosomal movement, the number and morphology of the mitochondria, and the fine structure of the cell. In the samples treated with the toxic compound the lysosomal movement changed, as did the morphology of the mitochondria and of the whole cells. The results are compared and discussed with regard to the results of conventional cytotoxicity tests performed in parallel. The new methods proved to be more sensitive and yielded more specific information on the cellular changes caused by the compound.

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细胞毒性检测的新方法:细胞内运动和线粒体特异性荧光定量视频显微镜。
本研究的目的是验证荧光和AVEC-DIC (Allen视频增强对比差干涉对比)显微技术在毒性检测中的应用。研究了有毒丙烯酸单体甲基丙烯酸乙酯(HEMA)对人成纤维细胞的影响。用HEMA浓度0.01 ~ 1%,孵育1 ~ 24 h。用AVEC-DIC显微镜和荧光染色观察细胞溶酶体运动速度、线粒体数量和形态以及细胞的精细结构。在用有毒化合物处理的样品中,溶酶体的运动发生了变化,线粒体和整个细胞的形态也发生了变化。将结果与平行进行的常规细胞毒性试验的结果进行比较和讨论。新方法被证明是更敏感的,并产生了更具体的信息,细胞变化引起的化合物。
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