York J L, Maddox L C, Zimniak P, McHugh T E, Grant D F
University of Arkansas for Medical Sciences, Little Rock 72205, USA.
Biotechniques. 1998 Oct;25(4):622-4, 626-8. doi: 10.2144/98254st03.
The reduction of the tetrazolium salt 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) to a blue formazan product is widely used for assaying cell survival and proliferation. The reduction reaction is catalyzed by dehydrogenases localized in the mitochondria of viable cells. As part of an analysis of the ability of glutathione S-transferase (GST) enzymes to protect cells from electrophilic compounds, we found extremely high background levels of the formazan product produced by cells that overexpressed the mouse GST P1-1 enzyme. Further analysis with purified GST enzymes confirmed the ability of these enzymes to reduce MTT in vitro. These data suggest that cytotoxicity assays using MTT should be interpreted with caution, especially when studying the effects of compounds that can influence GST expression.
将四唑盐3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四氮唑(MTT)还原为蓝色甲臜产物被广泛用于测定细胞存活和增殖。该还原反应由活细胞线粒体内的脱氢酶催化。作为对谷胱甘肽S-转移酶(GST)保护细胞免受亲电化合物影响能力分析的一部分,我们发现过表达小鼠GST P1-1酶的细胞产生的甲臜产物背景水平极高。用纯化的GST酶进行的进一步分析证实了这些酶在体外还原MTT的能力。这些数据表明,使用MTT的细胞毒性测定应谨慎解释,尤其是在研究可影响GST表达的化合物的作用时。