A microfluidic device for isolation and characterization of transendothelial migrating cancer cells

被引:28
作者
Cui, Xin [1 ]
Guo, Weijin [1 ]
Sun, Yubing [2 ]
Sun, Baoce [1 ]
Hu, Shuhuan [1 ]
Sun, Dong [1 ,3 ]
Lam, Raymond H. W. [1 ,3 ,4 ,5 ]
机构
[1] City Univ Hong Kong, Dept Mech & Biomed Engn, Kowloon, Hong Kong, Peoples R China
[2] Univ Massachusetts, Dept Mech & Ind Engn, Amherst, MA 01002 USA
[3] City Univ Hong Kong, Ctr Robot & Automat, Kowloon, Hong Kong, Peoples R China
[4] City Univ Hong Kong, Ctr Biosyst Neurosci & Nanotechnol, Kowloon, Hong Kong, Peoples R China
[5] City Univ Hong Kong, Shenzhen Res Inst, Shenzhen, Peoples R China
来源
BIOMICROFLUIDICS | 2017年 / 11卷 / 01期
基金
中国国家自然科学基金;
关键词
VASCULAR ENDOTHELIAL-CELLS; UP-REGULATION; FLOW; EXTRAVASATION; INVASION; CXCR4; CHIP; INVOLVEMENT; INTEGRATION; METASTASIS;
D O I
10.1063/1.4974012
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Transendothelial migration of cancer cells is a critical stage in cancer, including breast cancer, as the migrating cells are generally believed to be highly metastatic. However, it is still challenging for many existing platforms to achieve a fully covering endothelium and to ensure transendothelial migration capability of the extracted cancer cells for analyses with high specificity. Here, we report a microfluidic device containing multiple independent cell collection microchambers underneath an embedded endothelium such that the transendothelial-migrated cells can be selectively collected from only the microchambers with full coverage of an endothelial layer. In this work, we first optimize the pore size of a microfabricated supporting membrane for the endothelium formation. We quantify transendothelial migration rates of a malignant human breast cell type (MDA-MB-231) under different shear stress levels. We investigate characteristics of the migrating cells including morphology, cytoskeletal structures, and migration (speed and persistence). Further implementation of this endothelium-embedded microfluidic device can provide important insights into migration and intracellular characteristics related to cancer metastasis and strategies for effective cancer therapy. (C) 2017 Author(s).
引用
收藏
页数:12
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