An Application of Stream Imaging Technique in the Study of Osmotic Behaviors of Multiple Cells.

Hsiu-Hung Chen, Edward H Lin, Shelly Heimfeld, Dayong Gao
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Abstract

Light microscopy method offers unique abilities for the determination of membrane transport properties of either single or multiple cells. A stream imaging system composed of a microfluidic device, a charge-coupled device camera, and a microscope has been developed to study the osmotic behavior of multiple cells in response toward their extracellular environment. Cells of interest were first mixed with the desired extracellular medium and streamed into a microchannel. The microchannel confines the movement of the cells in a monolayer and allows cells to move along the flow direction only. The cells then pass through a sensing zone where the images of cells were capable of being captured under a microscope. Using mouse dendritic cells (mDCs) as a model system, the membrane transport properties were investigated. The kinetics volume changes of mDCs under various extracellular conditions at room temperature (22°C) were analyzed using a biophysical model to determine water and cryoprotectant transport properties of the cell membrane. This prototype system directly allows us to observe, trace, capture, and store the sample information in terms of number, concentration, dynamic size, or shape for further analyses and documentations. We believe that the system has the potential of being used as a stand-alone equipment, or integrated into a lab-on-a-chip system, or embedded into commercialized instruments.

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流成像技术在多细胞渗透行为研究中的应用。
光学显微镜法为测定单个或多个细胞的膜运输特性提供了独特的能力。本文研制了一种由微流控装置、电荷耦合器件相机和显微镜组成的流成像系统,用于研究多细胞对细胞外环境的渗透行为响应。首先将感兴趣的细胞与所需的细胞外培养基混合,并将其流到微通道中。微通道将细胞的运动限制在一个单层中,并且只允许细胞沿流动方向移动。然后细胞通过一个感应区,在那里细胞的图像可以在显微镜下被捕捉到。以小鼠树突状细胞(mDCs)为模型系统,研究了其膜转运特性。利用生物物理模型分析了室温(22°C)下不同胞外条件下mDCs的动力学体积变化,以确定细胞膜的水和冷冻保护剂运输特性。这个原型系统直接允许我们在数量、浓度、动态大小或形状方面观察、跟踪、捕获和存储样品信息,以便进一步分析和记录。我们相信该系统具有作为独立设备使用的潜力,或集成到芯片实验室系统中,或嵌入到商业化仪器中。
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