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一种用于单细胞水平分析的快速微流控切换系统。

A rapid microfluidic switching system for analysis at the single cellular level.

机构信息

Cardiovascular Physiology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, Okayama 700-8558, Japan.

出版信息

IEEE Trans Nanobioscience. 2009 Dec;8(4):306-11. doi: 10.1109/TNB.2009.2035253.

Abstract

Analysis of cellular responses to chemicals at high spatiotemporal resolution is required for precise understanding of intracellular signal transduction. Here, we demonstrated a novel method for applying different solutions to a part of or all of a cell at high spatiotemporal resolution. We fabricated a microfluidic device using polydimethylsiloxane, and the sharp interface between the two solution streams flowing in the channel was used for the application of different solutions. We constructed a computer-controlled system to control the interface movement precisely, rapidly, and reproducibly during positioning, and spatial and temporal resolutions attained were 1.6 mum and 189 ms, respectively. We then applied the present system to the analysis of intracellular responses to chemicals. We were able to measure [Ca (2+)] (i) increases within 500 ms, when one laminar stream covered a part of the cell. This method can be used as a generic platform to investigate responses against drugs at the single cell level.

摘要

为了精确理解细胞内信号转导,需要高时空分辨率分析细胞对化学物质的反应。在这里,我们展示了一种新的方法,可以在高时空分辨率上将不同的溶液施加到细胞的一部分或全部上。我们使用聚二甲基硅氧烷制造了微流控设备,并且在通道中流动的两种溶液流之间的锐利界面用于施加不同的溶液。我们构建了一个计算机控制的系统,以便在定位期间精确、快速和可重复地控制界面运动,并且所达到的空间和时间分辨率分别为 1.6 µm 和 189 ms。然后,我们将该系统应用于分析细胞内对化学物质的反应。当一个层流流覆盖细胞的一部分时,我们能够在 500 ms 内测量 [Ca(2+)](i)的增加。该方法可用作在单细胞水平上研究针对药物的反应的通用平台。

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