Department of Materials Science & Engineering, University of Washington, Seattle, WA 98195, USA.
Phys Biol. 2011 Feb;8(1):015006. doi: 10.1088/1478-3975/8/1/015006. Epub 2011 Feb 7.
The response of cells to a chemical or biological agent in terms of their impedance changes in real-time is a useful mechanism that can be utilized for a wide variety of biomedical and environmental applications. The use of a single-cell-based analytical platform could be an effective approach to acquiring more sensitive cell impedance measurements, particularly in applications where only diminutive changes in impedance are expected. Here, we report the development of an on-chip cell impedance biosensor with two types of electrodes that host individual cells and cell populations, respectively, to study its efficacy in detecting cellular response. Human glioblastoma (U87MG) cells were patterned on single- and multi-cell electrodes through ligand-mediated natural cell adhesion. We comparatively investigated how these cancer cells on both types of electrodes respond to an ion channel inhibitor, chlorotoxin (CTX), in terms of their shape alternations and impedance changes to exploit the fine detectability of the single-cell-based system. The detecting electrodes hosting single cells exhibited a significant reduction in the real impedance signal, while electrodes hosting confluent monolayer of cells showed little to no impedance change. When single-cell electrodes were treated with CTX of different doses, a dose-dependent impedance change was observed. This enables us to identify the effective dose needed for this particular treatment. Our study demonstrated that this single-cell impedance system may potentially serve as a useful analytical tool for biomedical applications such as environmental toxin detection and drug evaluation.
细胞对化学或生物制剂的反应表现在其阻抗的实时变化上,这是一种非常有用的机制,可以应用于广泛的生物医学和环境应用中。使用基于单细胞的分析平台可能是一种获取更敏感细胞阻抗测量的有效方法,特别是在预计阻抗只有微小变化的应用中。在这里,我们报告了一种具有两种电极的片上细胞阻抗生物传感器的开发,这两种电极分别承载单个细胞和细胞群体,以研究其在检测细胞反应方面的功效。通过配体介导的自然细胞黏附,将人类脑胶质瘤(U87MG)细胞模式化到单细胞和多细胞电极上。我们比较研究了这些癌细胞在这两种类型的电极上如何响应离子通道抑制剂氯毒素(CTX),从它们的形状变化和阻抗变化方面来利用单细胞系统的精细检测能力。承载单个细胞的检测电极的实际阻抗信号显著降低,而承载细胞融合单层的电极几乎没有阻抗变化。当用不同剂量的 CTX 处理单细胞电极时,观察到剂量依赖性的阻抗变化。这使我们能够确定这种特定治疗所需的有效剂量。我们的研究表明,这种单细胞阻抗系统可能作为一种有用的分析工具,用于生物医学应用,如环境毒素检测和药物评估。