In situ collagen assembly for integrating microfabricated three-dimensional cell-seeded matrices

被引:179
作者
Gillette, Brian M. [1 ]
Jensen, Jacob A. [1 ]
Tang, Beixian [1 ]
Yang, Genevieve J. [1 ]
Bazargan-Lari, Ardalan [1 ]
Zhong, Ming [1 ]
Sia, Samuel K. [1 ]
机构
[1] Columbia Univ, Dept Biomed Engn, New York, NY 10027 USA
基金
美国国家科学基金会;
关键词
D O I
10.1038/nmat2203
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Microscale fabrication of three-dimensional (3D) extracellular matrices (ECMs) can be used to mimic the often inhomogeneous and anisotropic properties of native tissues(1-3) and to construct in vitro cellular microenvironments(4-6). Cellular contraction of fibrous natural ECMs (such as fibrin and collagen I) can detach matrices from their surroundings and destroy intended geometry(7-9). Here, we demonstrate in situ collagen fibre assembly (the nucleation and growth of new collagen fibres from preformed collagen fibres at an interface) to anchor together multiple phases of cell-seeded 3D hydrogel-based matrices against cellular contractile forces. We apply this technique to stably interface multiple microfabricated 3D natural matrices (containing collagen I, Matrigel, fibrin or alginate); each phase can be seeded with cells and designed to permit cell spreading. With collagen-fibre-mediated interfacing, microfabricated 3D matrices maintain stable interfaces (the individual phases do not separate from each other) over long-term culture (at least 3 weeks) and support spatially restricted development of multicellular structures within designed patterns. The technique enables construction of well-defined and stable patterns of a variety of 3D ECMs formed by diverse mechanisms (including temperature-, ion- and enzyme-mediated crosslinking), and presents a simple approach to interface multiple 3D matrices for biological studies and tissue engineering.
引用
收藏
页码:636 / 640
页数:5
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