论文标题
通过电阻抗光谱法中Transwell插入物中的细胞屏障表征
Cell barrier characterization in transwell inserts by electrical impedance spectroscopy
论文作者
论文摘要
我们描述了一种基于阻抗的细胞屏障完整性测试方法。可以通过简单地将类似筷子的电极(STX-1)连接到允许在插入式插入物中培养的细胞屏障来实现四极电极电阻抗光谱(EIS)设置。随后的电阻抗的电路模型会导致屏障的电容性能旁边是众所周知的transepithepithial电阻(TEER)。通过对(a)不同的膜涂层材料的CACO-2单层的EIS分析,分析了新方法的多功能性,(b)两种不同的渗透性增强乙烯乙二醇 - 乙二醇 - 乙二醇(2-氨基乙基)-N,N,N,N,N,N,N',N',N',N'-Tetraaceticatic Acidatoration(Egta)和(Egta)和(Egta)和Saponin和Saponin和Saponin和Saponin和Saponin和Saponin和(C)。对于不同的膜涂料材料,标准方案和新方案的序列在培养过程中重合并增加,而电容对于三种不同的表面材料(无涂层,矩阵和胶原蛋白I)显示出明显的最大值。渗透性增强剂会导致TEER值下降,但仅皂苷会以两个数量级来改变细胞层的电容。因此,细胞层电容和Teer代表了表征单层的两个独立特性。使用类似商业筷子的电极来获取在Transwell插入物中培养的屏障的阻抗,可以对细胞屏障的行为显着洞察,而研究人员没有额外的工作。这种简单的方法可以演变为细胞屏障研究中使用的标准方案。
We describe an impedance-based method for cell barrier integrity testing. A four-electrode electrical impedance spectroscopy (EIS) setup can be realized by simply connecting a commercial chopstick-like electrode (STX-1) to a potentiostat allowing monitoring cell barriers cultivated in transwell inserts. Subsequent electric circuit modeling of the electrical impedance results the capacitive properties of the barrier next to the well-known transepithelial electrical resistance (TEER). The versatility of the new method was analyzed by the EIS analysis of a Caco-2 monolayer in response to (a) different membrane coating materials, (b) two different permeability enhancers ethylene glycol-bis(2-aminoethylether)-N,N,N',N'-tetraacetic acid (EGTA) and saponin, and (c) sonoporation. For the different membrane coating materials, the TEERs of the standard and new protocol coincide and increase during cultivation, while the capacitance shows a distinct maximum for three different surface materials (no coating, Matrigel, and collagen I). The permeability enhancers cause a decline in the TEER value, but only saponin alters the capacitance of the cell layer by two orders of magnitude. Hence, cell layer capacitance and TEER represent two independent properties characterizing the monolayer. The use of commercial chopstick-like electrodes to access the impedance of a barrier cultivated in transwell inserts enables remarkable insight into the behavior of the cellular barrier with no extra work for the researcher. This simple method could evolve into a standard protocol used in cell barrier research.