Automation of Three-Dimensional Cell Culture in Arrayed Microfluidic Devices

被引:35
作者
Montanez-Sauri, Sara I. [2 ]
Sung, Kyung Eun
Puccinelli, John P.
Pehlke, Carolyn
Beebe, David J. [1 ]
机构
[1] Univ Wisconsin, Wisconsin Inst Med Res, Dept Biomed Engn, Madison, WI 53705 USA
[2] Univ Wisconsin, Mat Sci Program, Madison, WI 53705 USA
来源
JALA | 2011年 / 16卷 / 03期
关键词
extracellular matrix; microfluidics; collagen; 3D; screening; EXTRACELLULAR-MATRIX; DIFFERENTIATION; MICROARRAY; BIOLOGY;
D O I
10.1016/j.jala.2011.02.003
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The increasing interest in studying the interactions between cells and the extracellular matrix (ECM) has created a need for high throughput low-cost three-dimensional (3D) culture systems. The recent development of tubeless microfluidics via passive pumping provides a high throughput microchannel culture platform compatible with existing high throughput infrastructures (e.g., automated liquid handlers). Here, we build on a previously reported high throughput two-dimensional system to create a robust automated system for 3D culture. Operational controls including temperature and sample handling have been characterized and automated. Human mammary fibroblasts (HMFs) suspended in type I collagen are loaded and cultured in microchannel arrays and used to optimize the system operational parameters. A Peltier cooler maintains the collagen as a liquid at 4 C during cell seeding, followed by polymerization at 37 C. Optimization of this platform is discussed (e.g., controlling collagen contraction, increasing cell viability, preventing the removal of microchannel contents), and 3D distribution of HMFs is examined by fluorescent microscopy. Finally, we validate the platform by automating a previously developed 3D breast carcinoma coculture assay. The platform allows more efficient 3D culture experiments and lays the foundation for high throughput studies of cell-ECM interactions. (JALA 2011;16:171-85)
引用
收藏
页码:171 / 185
页数:15
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