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用于对数灌注胚胎干细胞培养的微流控阵列

Microfluidic arrays for logarithmically perfused embryonic stem cell culture.

作者信息

Kim Lily, Vahey Michael D, Lee Hsu-Yi, Voldman Joel

机构信息

Massachusetts Institute of Technology, 77 Massachusetts Avenue, Rm 36-824, Cambridge, MA 02139, USA.

出版信息

Lab Chip. 2006 Mar;6(3):394-406. doi: 10.1039/b511718f. Epub 2006 Jan 25.

Abstract

We present a microfluidic device for culturing adherent cells over a logarithmic range of flow rates. The device sets flow rates through four separate cell-culture chambers using syringe-driven flow and a network of fluidic resistances. The design is easy to fabricate with no on-chip valves and is scalable both in the number of culture chambers as well as in the range of applied flow rates. Using particle velocimetry, we have characterized the flow-rate range. We have also demonstrated an extension of the design that combines the logarithmic flow-rate functionality with a logarithmic concentration gradient across the array. Using fluorescence measurements we have verified that a logarithmic concentration gradient was established in the extended device. Compared with static cell culture, both devices enable greater control over the soluble microenvironment by controlling the transport of molecules to and away from the cells. This approach is particularly relevant for cell types such as embryonic stem cells (ESCs) which are especially sensitive to the microenvironment. We have demonstrated for the first time culture of murine ESCs (mESCs) in continuous, logarithmically scaled perfusion for 4 days, with flow rates varying >300x across the array. Cells grown in the slowest flow rate did not proliferate, while colonies grown in higher flow rates exhibited healthy round morphology. We have also demonstrated logarithmically scaled continuous perfusion culture of 3T3 fibroblasts for 3 days, with proliferation at all flow rates except the slowest rate.

摘要

我们展示了一种微流控装置,用于在对数流速范围内培养贴壁细胞。该装置使用注射器驱动的流动和流体阻力网络来设置通过四个独立细胞培养室的流速。该设计易于制造,无需片上阀,并且在培养室数量以及应用流速范围内均可扩展。我们使用粒子测速法对流速范围进行了表征。我们还展示了该设计的一种扩展,即将对数流速功能与整个阵列上的对数浓度梯度相结合。通过荧光测量,我们验证了在扩展装置中建立了对数浓度梯度。与静态细胞培养相比,这两种装置都能通过控制分子向细胞和从细胞的运输,更好地控制可溶性微环境。这种方法对于诸如胚胎干细胞(ESC)等对微环境特别敏感的细胞类型尤为重要。我们首次展示了在连续、对数缩放的灌注条件下培养小鼠胚胎干细胞(mESC)4天,整个阵列上的流速变化超过300倍。在最低流速下生长的细胞不增殖,而在较高流速下生长的集落呈现出健康的圆形形态。我们还展示了对3T3成纤维细胞进行对数缩放的连续灌注培养3天,除了最低流速外,所有流速下细胞均有增殖。

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