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Chemically induced strong cellular hypertrophy often reduces the accuracy of cytotoxicity measurements obtained using the ATP assay

机译:化学诱导的强细胞肥大通常降低使用ATP测定获得的细胞毒性测量的准确性

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摘要

The ATP assay is a highly sensitive and versatile method for measuring cytotoxicity. However, the correlation between the cell viability results obtained using the ATP assay and those obtained using direct cell counting has not been widely reported. Therefore, to evaluate the reliability and limitations of the ATP assay, we compared the results of ATP assay with those of automatic cell counter, which can measure the number and diameter of cells directly, by using 24 compounds and repeating individual experiments thrice. The correlation between the data was low for 7 of the 24 compounds (r(2) < 0.8, at least 2 out of 3 experiments). These were the top 7 of the 11 compounds that induced cell hypertrophy. These 7 compounds were also observed to increase the area of mitochondria. However, the last 4 of the 11 compounds increased the cell size but did not increase the mitochondrial area. For the remaining 13 compounds, which had no effect on cell size, a good correlation was observed between the results of the two methods (r(2) > 0.8, at least 2 out of 3 experiments), and the cell size was effectively the same as that of the controls. We concluded that the poor correlation between the two methods was attributable to an increase in the content of intracellular ATP because of the chemically induced cell and mitochondrial hypertrophy. We showed that the ATP assay is unsuitable for assessing the cytotoxicity of compounds that induce cell hypertrophy with increase in the mitochondrial area and ATP content.
机译:ATP测定是一种用于测量细胞毒性的高度敏感和多功能的方法。然而,使用ATP测定和使用直接细胞计数获得的细胞活力与使用直接细胞计数的相比之下的相关性。因此,为了评估ATP测定的可靠性和限制,将ATP测定与自动细胞计数器的结果进行比较,其可以通过使用24种化合物和重复个体实验直接测量细胞的数量和直径。 24化合物中的7个(R(2)<0.8,3实验中的至少2个中的7个,数据之间的相关性低。这些是诱导细胞肥大的11种化合物的前7个。还观察到这7种化合物增加了线粒体面积。然而,11种化合物中的最后4种复合增加了细胞大小,但没有增加线粒体区域。对于剩余的13种化合物,其对细胞尺寸没有影响,在两种方法的结果(R(2)> 0.8的结果之间观察到良好的相关性,并且3实验中的至少2个),并且细胞大小有效地与控件相同。我们得出结论,由于化学诱导的细胞和线粒体肥大,两种方法之间的相关性差可归因于细胞内ATP的含量增加。我们表明ATP测定不适合评估诱导细胞肥大随着线粒体区域和ATP含量增加的细胞毒性的细胞毒性。

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