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ABC 转运蛋白影响荧光探针对细胞内氧化剂的检测。

ABC transporters affect the detection of intracellular oxidants by fluorescent probes.

机构信息

Department of Animal Physiology and Immunology, Institute of Experimental Biology, Faculty of Science, Masaryk University, Brno, Czech Republic.

出版信息

Free Radic Res. 2011 Jul;45(7):779-87. doi: 10.3109/10715762.2011.579120. Epub 2011 May 13.

Abstract

Intracellular production of reactive oxygen species (ROS) plays an important role in the control of cell physiology. For the assessment of intracellular ROS production, a plethora of fluorescent probes is commonly used. Interestingly, chemical structures of these probes imply they could be substrates of plasma membrane efflux pumps, called ABC transporters. This study tested whether the determination of intracellular ROS production and mitochondrial membrane potential by selected fluorescent probes is modulated by the expression and activity of ABC transporters. The sub-clones of the HL-60 cell line over-expressing MDR1, MRP1 and BCRP transporters were employed. ROS production measured by luminol- and L-012-enhaced chemiluminescence and cytochrome c reduction assay showed similar levels of ROS production in all the employed cell lines. It was proved that dihydrorhodamine 123, dihexiloxocarbocyanine iodide, hydroethidine, tetrachloro-tetraethylbenzimidazolocarbo-cyanine iodide and tetramethylrhodamine ethyl ester perchlorate are substrates for MDR1; dichlorodihydrofluoresceine, hydroethidine and tetramethylrhodamine ethyl ester perchlorate are substrates for MRP1; dichlorodihydrofluoresceine, dihydrorhodamine 123, hydroethidine and tetrachloro-tetraethylbenzimidazolocarbo-cyanine iodide are substrates for BCRP. Thus, the determination of intracellular ROS and mitochondrial potential by the selected probes is significantly altered by ABC transporter activities. The activity of these transporters must be considered when employing fluorescent probes for the assessment of ROS production or mitochondrial membrane potential.

摘要

细胞内活性氧(ROS)的产生在控制细胞生理中起着重要作用。为了评估细胞内 ROS 的产生,通常使用大量的荧光探针。有趣的是,这些探针的化学结构表明它们可能是质膜外排泵(称为 ABC 转运体)的底物。本研究测试了选定的荧光探针测定细胞内 ROS 产生和线粒体膜电位是否受 ABC 转运体的表达和活性调节。使用过度表达 MDR1、MRP1 和 BCRP 转运体的 HL-60 细胞系的亚克隆进行了研究。通过发光和 L-012 增强化学发光以及细胞色素 c 还原测定法测量 ROS 产生,结果表明所有使用的细胞系中 ROS 产生水平相似。证明二氢罗丹明 123、二己基氧羰氰碘化物、羟乙基二氢呋喃、四氯四乙基苯并咪唑碳酰氰碘化物和四甲基罗丹明乙酯高氯酸盐是 MDR1 的底物;二氯二氢荧光素、羟乙基二氢呋喃和四甲基罗丹明乙酯高氯酸盐是 MRP1 的底物;二氯二氢荧光素、二氢罗丹明 123、羟乙基二氢呋喃和四氯四乙基苯并咪唑碳酰氰碘化物是 BCRP 的底物。因此,所选探针测定细胞内 ROS 和线粒体电位的能力受到 ABC 转运体活性的显著影响。在使用荧光探针评估 ROS 产生或线粒体膜电位时,必须考虑这些转运体的活性。

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