细胞定心:一种新颖的技术,可以使用CYTOPATCH芯片实现细胞对细胞的自动贴片夹紧。

Receptors & channels Pub Date : 2003-01-01
Alfred Stett, Claus Burkhardt, Uli Weber, Peter van Stiphout, Thomas Knott
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引用次数: 0

摘要

全细胞配置的贴片夹紧悬浮细胞的自动装置必须(1)使孤立的细胞与贴片接触,(2)形成千兆密封,(3)建立稳定的细胞内通道,允许高质量的离子电流记录。平面衬底上的单个开口似乎是解决这些问题的有趣的简单方法,但由于整个细胞结构的形成率低,我们放弃了这种方法。单开口不适合通过吸吸将细胞吸引到开口,也不适合形成gigaseal并导致随后的膜破裂。为了用机械微观结构解决这三个任务,我们开发了所谓的细胞定心技术,应用于悬浮细胞的操作顺序与传统的贴片夹紧相同。用这种方法,我们从流动的悬浮液中选择细胞,通过吸力固定在贴片移液管的尖端,成功率为97%,形成千兆膜的成功率为68%。随后的全细胞记录和细胞内路西法黄染色证实了进入细胞质的稳定途径。目前,一种在微结构接触移液器周围的玻璃中嵌入吸口的芯片正在开发中。该CYTOPATCH芯片的加工工艺适合大批量生产。CYTOPATCH自动将允许全自动,并行和异步全细胞记录。
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CYTOCENTERING: a novel technique enabling automated cell-by-cell patch clamping with the CYTOPATCH chip.

Automats for patch clamping suspended cells in whole-cell configuration must (1) bring isolated cells in contact with patch contacts, (2) form gigaseals, and (3) establish stable intracellular access that allows for high quality recording of ionic currents. Single openings in planar substrates seem to be intriguing simple solutions for these problems, but due to the low rate of formation of whole-cell configurations we discarded this approach. Single openings are not suited for both attracting cells to the opening by suction and forming gigaseals with subsequent membrane rupture. To settle the three tasks with a mechanical microstructure we developed the socalled CYTOCENTERING technique to apply to suspended cells the same operation sequence as in conventional patch clamping. With this method we immobilized selected cells from a flowing suspension on the tip of a patch pipette by suction with a success rate of 97% and formed gigaseals with a success rate of 68%. Subsequent whole-cell recordings and intracellular staining with Lucifer yellow proved the stable access to the cytoplasm. Currently, a chip with an embedded suction opening in glass surrounding the microstructured contact pipette is under development. The processing of this CYTOPATCH chip is compatible to large-volume production. The CYTOPATCH automat will allow for fully automated, parallel, and asynchronous whole-cell recordings.

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