A perfusable microfluidic device with on-chip total internal reflection fluorescence microscopy (TIRFM) for in situ and real-time monitoring of live cells

被引:9
|
作者
Yokokawa, Ryuji [1 ,2 ]
Kitazawa, Yuko [1 ,2 ]
Terao, Kyohei [2 ,3 ]
Okonogi, Atsuhito [1 ,2 ]
Kanno, Isaku [1 ]
Kotera, Hidetoshi [1 ,2 ]
机构
[1] Kyoto Univ, Dept Microengn, Sakyo Ku, Kyoto 6068501, Japan
[2] Japan Sci & Technol Agcy JST, Core Res Evolut Sci & Technol CREST, Chiyoda Ku, Tokyo 1020076, Japan
[3] Kagawa Univ, Dept Intelligent Mech Syst Engn, Takamatsu, Kagawa 7610396, Japan
基金
日本科学技术振兴机构;
关键词
Total internal reflection fluorescent microscopy (TIRFM); Cell analysis; Microfluidics; INSULIN-SECRETION; DRUG DISCOVERY; BEHAVIOR;
D O I
10.1007/s10544-012-9656-5
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
A microfluidic device integrated with a Total Internal Reflection (TIR)-based chip for cell observation and analysis was developed. This integrated device enables in situ Total Internal Reflection Fluorescence Microscopy (TIRFM) on adherent cells cultured under continuous medium perfusion. This TIR-based chip, allows TIRFM to be easily performed on cells without the assembly of complicated optical components and cell culture chambers. The integrated device was evaluated by tracking the movement of fluorescent beads and monitoring the location of insulin granules in mouse pancreatic beta-cells. This system offers higher signal-to-noise (S/N) ratio than epi-fluorescence microscopy (EPIFM), and comparable image quality to commercial TIRFM systems when imaging insulin granules. We also detected repetitive changes in intracellular Ca2+ concentration in MIN6-m9 cells stimulated with KCl, which demonstrates quick perfusion for cell analysis while maintaining high S/N ratio.
引用
收藏
页码:791 / 797
页数:7
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