Imaging Division, UMC Utrecht, Heidelberglaan 100, 3584 CX, Utrecht, The Netherlands.
Department of Pharmaceutics, Ghent University, Ghent, Belgium.
Mol Imaging Biol. 2017 Oct;19(5):683-693. doi: 10.1007/s11307-016-1042-x.
The combination of ultrasound and microbubbles can facilitate cellular uptake of (model) drugs via transient permeabilization of the cell membrane. By using fluorescent molecules, this process can be studied conveniently with confocal fluorescence microscopy. This study aimed to investigate the relation between cellular uptake and fluorescence intensity increase of intercalating model drugs.
SYTOX Green, an intercalating fluorescent dye that displays >500-fold fluorescence enhancement upon binding to nucleic acids, was used as a model drug for ultrasound-induced cellular uptake. SYTOX Green uptake was monitored in high spatiotemporal resolution to qualitatively assess the relation between uptake and fluorescence intensity in individual cells. In addition, the kinetics of fluorescence enhancement were studied as a function of experimental parameters, in particular, laser duty cycle (DC), SYTOX Green concentration and cell line.
Ultrasound-induced intracellular SYTOX Green uptake resulted in local fluorescence enhancement, spreading throughout the cell and ultimately accumulating in the nucleus during the 9-min acquisition. The temporal evolution of SYTOX Green fluorescence was substantially influenced by laser duty cycle: continuous laser (100 % DC) induced a 6.4-fold higher photobleaching compared to pulsed laser (3.3 % DC), thus overestimating the fluorescence kinetics. A positive correlation of fluorescence kinetics and SYTOX Green concentration was found, increasing from 0.6 × 10 to 2.2 × 10 s for 1 and 20 μM, respectively. Finally, C6 cells displayed a 2.4-fold higher fluorescence rate constant than FaDu cells.
These data show that the temporal behavior of intracellular SYTOX Green fluorescence enhancement depends substantially on nuclear accumulation and not just on cellular uptake. In addition, it is strongly influenced by the experimental conditions, such as the laser duty cycle, SYTOX Green concentration, and cell line.
超声与微泡的联合作用可以通过短暂地使细胞膜通透性增加,促进(模型)药物进入细胞。通过使用荧光分子,该过程可以方便地通过共聚焦荧光显微镜进行研究。本研究旨在研究细胞摄取与嵌入型模型药物荧光强度增加之间的关系。
SYTOX Green 是一种嵌入型荧光染料,与核酸结合后荧光增强>500 倍,被用作超声诱导细胞摄取的模型药物。以高时空分辨率监测 SYTOX Green 的摄取,以定性评估单个细胞中摄取与荧光强度之间的关系。此外,还研究了荧光增强动力学作为实验参数的函数,特别是激光占空比(DC)、SYTOX Green 浓度和细胞系。
超声诱导的细胞内 SYTOX Green 摄取导致局部荧光增强,在 9 分钟的采集过程中,荧光扩散到整个细胞并最终积累在细胞核中。SYTOX Green 荧光的时间演化受到激光占空比的显著影响:与脉冲激光(3.3% DC)相比,连续激光(100% DC)诱导的光漂白高 6.4 倍,从而高估了荧光动力学。还发现荧光动力学与 SYTOX Green 浓度呈正相关,从 1 和 20 μM 时的 0.6×10 和 2.2×10 s 分别增加。最后,C6 细胞的荧光率常数比 FaDu 细胞高 2.4 倍。
这些数据表明,细胞内 SYTOX Green 荧光增强的时间行为主要取决于核积累,而不仅仅是细胞摄取。此外,它还受到实验条件的强烈影响,例如激光占空比、SYTOX Green 浓度和细胞系。