TER-Ox:同时监测上皮屏障功能(TER)和线粒体呼吸(Ox)

Tobias Naber, Katharina Winter, Joachim Wegener
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引用次数: 0

摘要

上皮屏障功能和细胞呼吸是健康和疾病的关键细胞表型,因此参与许多病理疾病的进展。因此,在药物开发中,利用适当的体外疾病模型广泛靶向分子驱动程序。到目前为止,屏障功能和代谢呼吸的量化必须在个体表型分析中进行,这使得不可能在较长时间内同时跟踪单个细胞层的变化。我们开发了一种检测平台,可以同时监测在无标记和无创的可渗透基质上培养的上皮屏障功能和细胞层的代谢活性。因此,我们设计了一个不锈钢测量室,能够结合阻抗光谱和比例荧光氧制图。在该平台中,屏障功能被量化为经上皮电阻(TER),而呼吸活动被表示为表观耗氧量(AOCR),因此该组合装置的名称为TER- ox。我们通过研究上皮细胞系MDCK-I、MDCK-II和A549来验证TER-Ox系统,涵盖了广泛的屏障密封性。将TER-Ox组合装置的结果与已建立的屏障功能(cellZscope®)和耗氧量(VisiSens TD®)的单独读数进行比较。此外,我们表明,当用影响电子传递链(抗霉素A和丙二苯)或屏障完整性(细胞松弛素D)的调节剂处理细胞层时,这两个参数的差异很容易监测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

TER-Ox: Simultaneous Monitoring of Epithelial Barrier Function (TER) and Mitochondrial Respiration (Ox)

TER-Ox: Simultaneous Monitoring of Epithelial Barrier Function (TER) and Mitochondrial Respiration (Ox)

Epithelial barrier function and cellular respiration are key cellular phenotypes in health and disease and as such involved in the progression of many pathological disorders. Accordingly, the molecular drivers are targeted extensively in drug development using appropriate disease models in vitro. So far, quantification of barrier function and metabolic respiration had to be conducted in individual phenotypic assays, making it impossible to track changes simultaneously in a single cell layer over longer periods. We have developed an assay platform that allows for simultaneous monitoring of both, the epithelial barrier function and metabolic activity of cell layers cultured on permeable substrates label-free and non-invasively. Therefore, we designed a stainless-steel measurement chamber capable of combining impedance spectroscopy and ratiometric fluorescence-based oxygen mapping. In this platform, the barrier function is quantified as the transepithelial electrical resistance (TER) while the respiratory activity is expressed as the apparent oxygen consumption rate (AOCR) yielding the name TER-Ox for the combined setup. We validated the TER-Ox system by studying the epithelial cell lines MDCK-I, MDCK-II, and A549, covering a wide range of barrier tightness. Results of the combined TER-Ox setup were compared to established but individual readouts of barrier function (cellZscope®) and oxygen consumption (VisiSens TD®). Also, we show that differences in both parameters are readily monitored while treating cell layers with modulators affecting the electron transport chain (Antimycin A and malonoben) or barrier integrity (Cytochalasin D).

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