Biomanufacturing Research Institute and Technology Enterprises, Department of Pharmaceutical Sciences, North Carolina Central University, Durham, NC 27707, USA.
Biosens Bioelectron. 2010 Jun 15;25(10):2225-31. doi: 10.1016/j.bios.2010.02.029. Epub 2010 Mar 3.
In this study, the electric cell-substrate impedance sensing (ECIS) system was used to study the cellular activities of oral squamous cell carcinoma (OSCC) cells in a real-time and label-free manner. Various cellular activities, including cell adhesion, spreading, proliferation, and drug-induced apoptosis and inhibition of apoptosis, were monitored. A linear relationship was found between the impedance-based cell index and the cell number in the range of 3500 to 35,000 cells/well. Anti-cancer drug-cisplatin-induced OSCC cell apoptosis at the minimal concentration of 5 microM after 20 h of treatment and followed a linear dose-dependent manner in the concentration range from 10 microM to 25 microM. The inhibition of cisplatin-induced apoptosis by the carcinogen, nicotine, at concentrations from 0.1 microM to 10 microM was monitored. The most significant inhibitory effect of nicotine on cisplatin-induced apoptosis was observed at concentrations of 0.5-1 microM. The results obtained with impedance method correlated well with microscopic imaging analysis of cellular morphology and cell viability analysis. This study demonstrated that the impedance-based method can provide real-time information about the cellular activity of viable cells and detect drug-induced cellular activities much earlier than commonly used cell-based image analysis. This impedance-based method has the potential to provide a useful analytical approach for cancer research.
在这项研究中,我们使用了电细胞-基质阻抗感应(ECIS)系统以无标记的实时方式研究口腔鳞状细胞癌(OSCC)细胞的细胞活性。监测了各种细胞活性,包括细胞黏附、铺展、增殖以及药物诱导的细胞凋亡和抗凋亡作用。在 3500 到 35000 个细胞/孔的范围内,发现基于阻抗的细胞指数与细胞数量之间存在线性关系。抗癌药物顺铂在 20 小时的治疗后以 5 μM 的最小浓度诱导 OSCC 细胞凋亡,并在 10 μM 到 25 μM 的浓度范围内呈线性剂量依赖性。监测了致癌物质尼古丁在 0.1 μM 到 10 μM 的浓度范围内对顺铂诱导的细胞凋亡的抑制作用。在 0.5-1 μM 的浓度下,尼古丁对顺铂诱导的细胞凋亡的抑制作用最为显著。阻抗法获得的结果与细胞形态学的显微镜成像分析和细胞活力分析相关性良好。本研究表明,基于阻抗的方法可以提供有关活细胞细胞活性的实时信息,并比常用的基于细胞的图像分析更早地检测到药物诱导的细胞活性。这种基于阻抗的方法有可能为癌症研究提供一种有用的分析方法。