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A microfluidic bioreactor with integrated transepithelial electrical resistance (TEER) measurement electrodes for evaluation of renal epithelial cells

机译:具有集成的跨上皮电阻(TEER)测量电极的微流体生物反应器,用于评估肾上皮细胞

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摘要

We have developed a bilayer microfluidic system with integrated transepithelial electrical resistance (TEER) measurement electrodes to evaluate kidney epithelial cells under physiologically relevant fluid flow conditions. The bioreactor consists of apical and basolateral fluidic chambers connected via a transparent microporous membrane. The top chamber contains microfluidic channels to perfuse the apical surface of the cells. The bottom chamber acts as a reservoir for transport across the cell layer and provides support for the membrane. TEER electrodes were integrated into the device to monitor cell growth and evaluate cell–cell tight junction integrity. Immunofluorescence staining was performed within the microchannels for ZO-1 tight junction protein and acetylated Α-tubulin (primary cilia) using human renal epithelial cells (HREC) and MDCK cells. HREC were stained for cytoskeletal F-actin and exhibited disassembly of cytosolic F-actin stress fibers when exposed to shear stress. TEER was monitored over time under normal culture conditions and after disruption of the tight junctions using low Ca 2+ medium. The transport rate of a fluorescently labeled tracer molecule (FITC-inulin) was measured before and after Ca 2+ switch and a decrease in TEER corresponded with a large increase in paracellular inulin transport. This bioreactor design provides an instrumented platform with physiologically meaningful flow conditions to study various epithelial cell transport processes. Biotechnol. Bioeng. 2010;107:707–716. © 2010 Wiley Periodicals, Inc.
机译:我们已经开发了具有集成跨上皮电阻(TEER)测量电极的双层微流体系统,以评估在生理相关的流体流动条件下的肾上皮细胞。生物反应器由通过透明微孔膜连接的顶端和基底外侧流体腔组成。顶部腔室包含微流体通道以灌注细胞的顶表面。底部腔室充当用于跨细胞层运输的储存器并为膜提供支撑。 TEER电极已集成到设备中,以监测细胞生长并评估细胞间紧密连接的完整性。使用人肾上皮细胞(HREC)和MDCK细胞在ZO-1紧密连接蛋白和乙酰化A-微管蛋白(原纤毛)的微通道内进行了免疫荧光染色。 HREC的细胞骨架F-肌动蛋白染色,并在暴露于剪切应力时表现出胞质F-肌动蛋白应激纤维的分解。在正常培养条件下以及在使用低Ca 2+培养基破坏紧密连接后,随时间监测TEER。在Ca 2+转换之前和之后,测量了荧光标记的示踪分子(FITC-菊粉)的传输速率,TEER的降低与副细胞菊粉传输的大幅增加相对应。这种生物反应器设计为仪器平台提供了具有生理意义的流动条件,以研究各种上皮细胞的运输过程。生物技术。生恩2010; 107:707-716。 ©2010 Wiley Periodicals,Inc.

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