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Single cell studies of mouse embryonic stem cell (mESC) differentiation by electrical impedance measurements in a microfluidic device

机译:在微流控设备中通过电阻抗测量对小鼠胚胎干细胞(mESC)进行分化的单细胞研究

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摘要

Biological populations of cells show considerable cell-to-cell variability. Study of single cells and analysis of cell heterogeneity are considered to be critical in understanding biological processes such as stem cell differentiation and cancer development. Recent advances in lab-on-a-chip techniques have allowed single-cell capture in microfluidic channels with the possibility of precise environmental control and high throughput of experiments with minimal usage of samples and reagents. In recent years, label-free techniques such as electrical impedance spectroscopy have emerged as a non-invasive approach to studying cell properties. In this study, we have designed and fabricated a microfluidic device that combines hydrodynamic trapping of single cells in pre-defined locations with the capability of running electrical impedance measurements within the same device. We have measured mouse embryonic stem cells (mESCs) at different states during differentiation (t=0 h, 24 h and 48 h) and quantitatively analysed the changes in electrical parameters of cells during differentiation. A marked increase in the magnitude of the cell impedance is found during cell differentiation, which can be attributed to an increase in cell size. The analysis of the measurements shows that the nucleus-to-cytoplasm ratio decreases during this process. The degree of cell heterogeneity is observed to be the highest when the cells are at the transition state (24 h), compare with cells at undifferentiated (0 h) and fully differentiated (48 h) states. The device enables highly efficient single cell trapping and provides sensitive, label-free electrical impedance measurements of individual cells, enabling the possibility of quantitatively analysing their physical state as well as studying the associated heterogeneity of a cell population.
机译:细胞的生物种群显示出很大的细胞间变异性。单细胞的研究和细胞异质性的分析被认为对于理解生物学过程(例如干细胞分化和癌症发展)至关重要。芯片实验室技术的最新进展已允许在微流体通道中捕获单细胞,并且可以进行精确的环境控制,并且在不使用样品和试剂的情况下就可以实现较高的实验通量。近年来,无标记技术(例如电阻抗光谱法)已经成为研究细胞特性的一种非侵入性方法。在这项研究中,我们设计和制造了一种微流体设备,该设备将单个位置的单个单元的流体动力捕获与在同一设备中运行电阻抗测量的能力结合在一起。我们已经在分化过程中(t = 0h,24h和48h)的不同状态下测量了小鼠胚胎干细胞(mESCs),并定量分析了分化过程中细胞电参数的变化。在细胞分化期间发现细胞阻抗的大小显着增加,这可以归因于细胞大小的增加。测量的分析表明,在此过程中,核质比降低了。当细胞处于过渡状态(24 h)时,观察到细胞异质性程度最高,与未分化(0 h)和完全分化(48 h)状态的细胞相比。该设备可实现高效的单细胞捕获,并提供单个细胞的灵敏,无标记的电阻抗测量值,从而能够定量分析其物理状态以及研究相关的细胞群异质性。

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