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

机译:一种微流体生物反应器,具有集成的TRANSEPITHELIAL电阻(TEER)测量电极,用于评估肾上皮细胞

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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.
机译:我们开发了一种双层微流体系统,具有集成的TRANSEPITHELIAL电阻(TEER)测量电极,在生理相关的流体流动条件下评估肾上皮细胞。生物反应器由通过透明微孔膜连接的顶端和基石流体腔室组成。顶室包含微流体通道以灌注细胞的顶端表面。底部腔室用作用于穿过细胞层的储存器,并为膜提供载体。将转向电极集成到装置中以监测细胞生长并评估细胞 - 细胞紧密结完整性。使用人肾上皮细胞(HREC)和MDCK细胞在ZO-1紧密结蛋白和乙酰化α-微管蛋白(原发性纤毛)的微通道内进行免疫荧光染色。当暴露于剪切应力时,为细胞骨架F-肌动蛋白染成细胞骨架F-肌动蛋白的拆卸,并在暴露于剪切应力时显示出脱索肌肌动蛋白应激纤维。在正常培养条件下随着时间的推移和使用低Ca〜(2+)培养基的紧密交叉点破坏而导致的人权。在Ca〜(2+)开关之前和之后测量荧光标记的示踪分子(FITC-菊粉)的运输速率,并且通过荚膜菊粉转运的大量增加,转型的降低。这种生物反应器设计提供仪表平台,具有生理上有意义的流动条件,以研究各种上皮细胞运输过程。 Biotechnol。生物。 2010; 107:707-716。

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