On-chip cell migration assay using microfluidic channels

被引:130
|
作者
Nie, Fu-Qiang
Yamada, Masumi
Kobayashi, Jun
Yamato, Masayuki
Kikuchi, Akihiko
Okano, Teruo
机构
[1] Tokyo Womens Med Univ, Inst Adv Biomed Engn & Sci, Shinjuku Ku, Tokyo 1628666, Japan
[2] Japan Sci & Technol Agcy, CREST, Kawaguchi, Saitama 3320012, Japan
基金
日本学术振兴会; 日本科学技术振兴机构;
关键词
cell migration; laminar flow; chemoattractant; microfluidic device;
D O I
10.1016/j.biomaterials.2007.05.037
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Cell migration plays a crucial role in various biological processes including embryogenesis, wound healing, immune response, and tissue development. Conventional cell migration assays for screening of chemo-attractants or -repellants are initiated by physical scraping of a portion of confluent cells on normal culture surfaces. However, this protocol requires both a large number of cells and an increased amount of reagents. Additionally, these methods are not suitable for scaling-up for high-throughput screening. Here, we show on-chip cell migration assay utilizing microfluidic channels. Laminar flow of trypsin solution in microfluidic channels achieved well-in controlled cell detachment of a portion of confluent cell monolayers, which could effectively pattern wound edges to mimic biological wounding in vivo. Trypsin laminar flow in precisely fabricated microfluidic devices enables accurate and reliable cell migration assay with limited amounts of reagents to either promote or inhibit cell migration. (C) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4017 / 4022
页数:6
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