Lewis Daniel M, Mavrogiannis Nicholas, Gagnon Zachary, Gerecht Sharon
Department of Chemical and Biomolecular Engineering, Johns Hopkins University, Baltimore, Maryland 21218, USA.
Biomicrofluidics. 2018 May 15;12(4):042202. doi: 10.1063/1.5026901. eCollection 2018 Jul.
Electric cell-substrate impedance sensing (ECIS) is a quickly advancing field to measure the barrier function of endothelial cells. Most ECIS systems that are commercially available use gold electrodes, which are opaque and do not allow for real-time imaging of cellular responses. In addition, most ECIS systems have a traditional tissue culture Petri-dish set up. This conventional set-up does not allow the introduction of physiologically relevant shear stress, which is crucial for the endothelial cell barrier function. Here, we created a new ECIS micro-bioreactor (MBR) that incorporates a clear electrode made of indium tin oxide in a microfluidic device. Using this device, we demonstrate the ability to monitor the barrier function along culture of cells under varying flow rates. We show that while two cell types align in the direction of flow in responses to high shear stress, they differ in the barrier function. Additionally, we observe a change in the barrier function in response to chemical perturbation. Following exposure to EDTA that disrupts cell-to-cell junctions, we could not observe distinct morphological changes but measured a loss of impedance that could be recovered with EDTA washout. High magnification imaging further demonstrates the loss and recovery of the barrier structure. Overall, we establish an ECIS MBR capable of real-time monitoring of the barrier function and cell morphology under shear stress and allowing high-resolution analysis of the barrier structure.
电细胞-基质阻抗传感(ECIS)是一个快速发展的用于测量内皮细胞屏障功能的领域。大多数市售的ECIS系统使用金电极,这种电极不透明,无法对细胞反应进行实时成像。此外,大多数ECIS系统采用传统的组织培养培养皿设置。这种传统设置不允许引入对内皮细胞屏障功能至关重要的生理相关剪切应力。在此,我们创建了一种新的ECIS微生物反应器(MBR),它在微流控装置中集成了由氧化铟锡制成的透明电极。使用该装置,我们展示了在不同流速下监测细胞培养过程中屏障功能的能力。我们表明,虽然两种细胞类型在高剪切应力下会沿流动方向排列,但它们在屏障功能上存在差异。此外,我们观察到屏障功能会因化学扰动而发生变化。在暴露于破坏细胞间连接的乙二胺四乙酸(EDTA)后,我们未观察到明显的形态变化,但测量到阻抗损失,而通过冲洗EDTA可以恢复。高倍成像进一步证明了屏障结构的损失和恢复。总体而言,我们建立了一种能够在剪切应力下实时监测屏障功能和细胞形态,并允许对屏障结构进行高分辨率分析的ECIS MBR。