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一种用于在开放获取培养中生成锐利梯度的微流控平台。

A microfluidic platform for generation of sharp gradients in open-access culture.

机构信息

Department of Bioengineering, University of Washington, Seattle, Washington 98195, USA.

出版信息

Biomicrofluidics. 2010 Nov 2;4(4):44105. doi: 10.1063/1.3490784.

Abstract

Control of the 3D microenvironment for cultured cells is essential for understanding the complex relationships that biomolecular concentration gradients have on cellular growth, regeneration, and differentiation. This paper reports a microfluidic device for delivering gradients of soluble molecules to cells in an open reservoir without exposing the cells to flow. The cells are cultured on a polyester membrane that shields them from the flow that delivers the gradient. A novel "lid" design is implemented which prevents leakage from around the membrane without requiring sealing agents or adhesives. Once layers are molded, device fabrication can be performed within minutes while at room temperature. Surface gradients were characterized with epifluorescence microscopy; image analysis verified that sharp gradients (∼33 μm wide) can be reproducibly generated. We show that heterogeneous laminar flow patterns of Orange and Green Cell Tracker (CT) applied beneath the membrane can be localized to cells cultured on the other side; concentration profile scans show the extent of CT diffusion parallel to the membrane's surface to be 10-20 μm. Our device is ideal for conventional cell culture because the cell culture surface is readily accessible to physical manipulation (e.g., micropipette access), the cell culture medium is in direct contact with the incubator atmosphere (i.e., no special protocols for ensuring proper equilibration of gas concentrations are required), and the cells are not subjected to flow-induced shear forces, which are advantageous attributes not commonly found in closed-channel microfluidic designs.

摘要

控制培养细胞的 3D 微环境对于理解生物分子浓度梯度对细胞生长、再生和分化的复杂关系至关重要。本文报道了一种用于向开放储液器中的细胞传递可溶性分子梯度的微流控装置,而不会使细胞暴露于流动中。细胞在聚酯膜上培养,该膜可防止细胞受到输送梯度的流动的影响。实施了新颖的“盖子”设计,可防止膜周围泄漏,而无需密封剂或粘合剂。一旦成型,设备可以在室温下几分钟内完成制造。使用落射荧光显微镜对表面梯度进行了表征;图像分析证实可以可重复地生成锐利的梯度(∼33 μm 宽)。我们表明,在膜下方施加的橙色和绿色细胞追踪剂(CT)的不均匀层流模式可以定位到另一侧培养的细胞;浓度分布扫描表明 CT 沿膜表面的扩散程度为 10-20 μm。我们的设备非常适合传统的细胞培养,因为细胞培养表面易于进行物理操作(例如,微吸管进入),细胞培养液与孵育箱气氛直接接触(即,不需要特殊的协议来确保气体浓度的适当平衡),并且细胞不受流致剪切力的影响,这是在封闭通道微流控设计中不常见的有利属性。

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