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Analysing calcium signalling of cells under high shear flows using discontinuous dielectrophoresis

机译:使用不连续介电电泳分析高剪切流下细胞的钙信号传导

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摘要

Immobilisation of cells is an important feature of many cellular assays, as it enables the physical/chemical stimulation of cells; whilst, monitoring cellular processes using microscopic techniques. Current approaches for immobilising cells, however, are hampered by time-consuming processes, the need for specific antibodies or coatings, and adverse effects on cell integrity. Here, we present a dielectrophoresis-based approach for the robust immobilisation of cells, and analysis of their responses under high shear flows. This approach is quick and label-free, and more importantly, minimises the adverse effects of electric field on the cell integrity, by activating the field for a short duration of 120 s, just long enough to immobilise the cells, after which cell culture media (such as HEPES) is flushed through the platform. In optimal conditions, at least 90% of the cells remained stably immobilised, when exposed to a shear stress of 63 dyn/cm2. This approach was used to examine the shear-induced calcium signalling of HEK-293 cells expressing a mechanosensitive ion channel, transient receptor potential vaniloid type 4 (TRPV4), when exposed to the full physiological range of shear stress.
机译:细胞的固定化是许多细胞测定法的重要特征,因为它可以刺激细胞的物理/化学过程。同时,使用微观技术监测细胞过程。然而,目前的固定细胞的方法受到耗时的过程,对特异性抗体或包被的需求以及对细胞完整性的不利影响所困扰。在这里,我们提出了一种基于介电电泳的方法,用于细胞的牢固固定,以及在高剪切流下分析其反应。这种方法是快速且无标签的,更重要的是,通过在短短120 s内激活电场(足以固定细胞),将电场对细胞完整性的不利影响最小化,此后细胞培养基(例如HEPES)通过平台冲洗。在最佳条件下,当受到63 dyn / cm 2 的剪切应力时,至少90%的细胞保持稳定固定。当暴露于剪切应力的整个生理范围时,该方法用于检查剪切诱导的表达机械敏感离子通道的HEK-293细胞的钙信号传导,该通道为瞬态受体电位4型(TRPV4)。

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