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贴壁哺乳动物细胞微流控灌注培养实用指南。

A practical guide to microfluidic perfusion culture of adherent mammalian cells.

作者信息

Kim Lily, Toh Yi-Chin, Voldman Joel, Yu Hanry

机构信息

Department of Electrical Engineering and Computer Science, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Rm 36-824, Cambridge, MA 02139, USA.

出版信息

Lab Chip. 2007 Jun;7(6):681-94. doi: 10.1039/b704602b. Epub 2007 May 11.

Abstract

Culturing cells at microscales allows control over microenvironmental cues, such as cell-cell and cell-matrix interactions; the potential to scale experiments; the use of small culture volumes; and the ability to integrate with microsystem technologies for on-chip experimentation. Microfluidic perfusion culture in particular allows controlled delivery and removal of soluble biochemical molecules in the extracellular microenvironment, and controlled application of mechanical forces exerted via fluid flow. There are many challenges to designing and operating a robust microfluidic perfusion culture system for routine culture of adherent mammalian cells. The current literature on microfluidic perfusion culture treats microfluidic design, device fabrication, cell culture, and micro-assays independently. Here we systematically present and discuss important design considerations in the context of the entire microfluidic perfusion culture system. These design considerations include the choice of materials, culture configurations, microfluidic network fabrication and micro-assays. We also present technical issues such as sterilization; seeding cells in both 2D and 3D configurations; and operating the system under optimized mass transport and shear stress conditions, free of air-bubbles. The integrative and systematic treatment of the microfluidic system design and fabrication, cell culture, and micro-assays provides novices with an effective starting point to build and operate a robust microfludic perfusion culture system for various applications.

摘要

在微观尺度上培养细胞能够控制微环境线索,如细胞间和细胞与基质的相互作用;具备扩大实验规模的潜力;可使用少量培养体积;并且能够与微系统技术集成以进行芯片上的实验。特别是微流控灌注培养允许在细胞外微环境中对可溶性生化分子进行可控的递送和去除,并通过流体流动对施加的机械力进行可控应用。为贴壁哺乳动物细胞的常规培养设计和操作一个强大的微流控灌注培养系统存在许多挑战。当前关于微流控灌注培养的文献将微流控设计、器件制造、细胞培养和微分析独立看待。在此,我们在整个微流控灌注培养系统的背景下系统地介绍并讨论重要的设计考虑因素。这些设计考虑因素包括材料的选择、培养配置、微流控网络制造和微分析。我们还介绍了诸如灭菌等技术问题;以二维和三维配置接种细胞;以及在优化的传质和剪切应力条件下、无气泡地操作系统。对微流控系统设计与制造、细胞培养和微分析进行综合系统的论述,为新手提供了一个有效的起点,以便构建和操作一个强大的微流控灌注培养系统用于各种应用。

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