A gel-free 3D microfluidic cell culture system

被引:163
作者
Ong, Siew-Min [1 ,2 ]
Zhang, Chi [1 ,2 ,3 ]
Toh, Yi-Chin [1 ]
Kim, So Hyun [4 ]
Foo, Hsien Loong [1 ,3 ]
Tan, Choon Hong [3 ,5 ]
van Noort, Danny [1 ]
Park, Sungsu [4 ]
Yu, Hanry [1 ,2 ,3 ,6 ,7 ,8 ,9 ]
机构
[1] ASTAR, Inst Bioengn & Nanotechnol, Singapore 138669, Singapore
[2] NUS, Grad Sch Integrat Sci & Engn, Ctr Life Sci, Singapore 117456, Singapore
[3] Ctr Life Sci, Grad Program Bioengn, Singapore 117456, Singapore
[4] Ewha Womans Univ, Div Nano Sci, Seoul 120750, South Korea
[5] Natl Univ Singapore, Fac Sci, Dept Chem, Singapore 117543, Singapore
[6] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Physiol, Singapore 117595, Singapore
[7] Singapore MIT Alliance, Singapore 117576, Singapore
[8] Natl Univ Singapore, DSO Labs, NUS Tissue Engn Programme, Singapore 117597, Singapore
[9] Natl Univ Singapore Hosp, Dept Hematol Oncol, Singapore 119074, Singapore
基金
英国医学研究理事会;
关键词
3D in vitro cell culture; cell aggregates; microfluidics; perfusion culture; transient inter-cellular polymeric linker; hydrogel;
D O I
10.1016/j.biomaterials.2008.04.022
中图分类号
R318 [生物医学工程];
学科分类号
0831 [生物医学工程];
摘要
3D microfluidic cell culture systems offer a biologically relevant model to conduct micro-scale mammalian cell-based research and applications. Various natural and synthetic hydrogels have been successfully incorporated into microfluidic systems to support mammalian cells in 3D. However, embedment of cells in hydrogels introduces operational complexity, potentially hinders mass transfer, and is not suitable for establishing cell-dense, ECM-poor constructs. We present here a gel-free method for seeding and culturing mammalian cells three-dimensionally in a microfluidic channel. A combination of transient inter-cellular polymeric linker and micro-fabricated pillar arrays was used for the in situ formation and immobilization of 3D multi-cellular aggregates in a microfluidic channel. 3D cellular constructs formed this way are relieved of hydrogel embedment for cellular support. Two mammalian cell lines (A549 and C3A) and a primary mammalian cell (bone marrow mesenchymal stem cells) were cultured in the gel-free 3D microfluidic cell culture system. The cells displayed 3D cellular morphology, cellular functions and differentiation capability, affirming the versatility of the system as a 3D cell perfusion culture platform for anchorage-dependent mammalian cells. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3237 / 3244
页数:8
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