Department of Civil Engineering and Computer Science, University of Rome Tor Vergata, 00133, Rome, Italy.
Department of Experimental Medicine, University of Rome Tor Vergata, 00133, Rome, Italy.
Biosens Bioelectron. 2020 Feb 15;150:111887. doi: 10.1016/j.bios.2019.111887. Epub 2019 Nov 20.
The study and the characterization of cell death mechanisms are fundamental in cell biology research. Traditional death/viability assays usually involve laborious sample preparation and expensive equipment or reagents. In this work, we use electrical impedance spectroscopy as a label-free methodology to characterize viable, necrotic and apoptotic human lymphoma U937 cells. A simple three-electrode coplanar layout is used in a differential measurement scheme and thousands of cells are measured at high-throughput (≈200 cell/s). Tailored signal processing enables accurate and robust cell characterization without the need for cell focusing systems. The results suggest that, at low frequency (0.5 MHz), signal magnitude enables the discrimination between viable/necrotic cells and cell fragments, whereas phase information allows discriminating between viable cells and necrotic cells. At higher frequency (10 MHz) two subpopulations of cell fragments are distinguished. This work substantiates the prominent role of electrical impedance spectroscopy for the development of next-generation cell viability assays.
细胞死亡机制的研究和特征分析是细胞生物学研究的基础。传统的死亡/存活检测方法通常需要繁琐的样本制备和昂贵的设备或试剂。在这项工作中,我们使用电阻抗谱作为一种无标记的方法来表征人类淋巴瘤 U937 细胞的存活、坏死和凋亡状态。采用简单的三电极共面布局进行差分测量方案,可实现高通量(≈200 个细胞/秒)测量数千个细胞。经过专门设计的信号处理,可以在无需细胞聚焦系统的情况下,实现准确而稳健的细胞特征分析。结果表明,在低频(0.5MHz)下,信号幅度可区分存活/坏死细胞和细胞碎片,而相位信息可区分存活细胞和坏死细胞。在更高的频率(10MHz)下,可以区分出两个细胞碎片亚群。这项工作证实了电阻抗谱在开发下一代细胞活力检测方法中的重要作用。