4.5 Article

A microwell array device with integrated microfluidic components for enhanced single-cell analysis

期刊

ELECTROPHORESIS
卷 30, 期 24, 页码 4166-4171

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/elps.200900572

关键词

Cell culture; Microfluidics; Micropumps; Microwells; Single-cell analysis

资金

  1. Ministry of Education, Culture, Sports, Science and Technology (MEXT) of Japan [20300149]
  2. Grants-in-Aid for Scientific Research [20300149] Funding Source: KAKEN

向作者/读者索取更多资源

Increasing awareness of the importance of cell heterogeneity in many biological and medical contexts is prompting increasing interest in systems that allow single-cell analysis rather than conventional bulk analysis (which provides average values for variables of interest from large numbers of cells). Recently, we presented a microwell chip for long-term, high-throughput single-cell analysis. The chip has proved to be useful for purposes such as screening individual cancer and stem cells for protein/gene markers. However, liquids in the wells can only be added or changed by manually rinsing the chip, or parts of it. This procedure has several well-known drawbacks - including risks of cross-contamination, large dead volumes and laboriousness - but there have been few previous attempts to integrate liquid rinsing/switching channels in ready-to-use systems for single-cell analysis. Here we present a microwell system designed (using flow simulations) for single-cell analysis with integrated microfluidic components (microchannels, magnetically driven micropumps and reservoirs) for supplying the cell culture wells with reagents, or rinsing, thus facilitating controlled, directed liquid handling. It can be used totally independently, since tubing is not essential. The practical utility of the integrated system has been demonstrated by culturing endothelial cells in the microwells, and successfully applying live-cell Calcein AM staining. Systems such as this combining high-density microwell chips with microfluidic components have great potential in numerous screening applications, such as exploring the important, but frequently undetected, heterogeneity in drug responses among individual cells.

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