A chip-based platform for the in vitro generation of tissues in three-dimensional organization

被引:76
作者
Gottwald, Eric
Giselbrecht, Stefan
Augspurger, Caroline
Lahni, Brigitte
Dambrowsky, Nina
Truckenmueller, Roman
Piotter, Volker
Gietzelt, Thomas
Wendt, Oliver
Pfleging, Wilhelm
Welle, Alex
Rolletschek, Alexandra
Wobus, Anna M.
Weibezahn, Karl-Friedrich
机构
[1] Forschungszentrum Karlsruhe, Inst Biol Interfaces, D-76344 Eggenstein Leopoldshafen, Germany
[2] Tech Univ Ilmenau, Inst Micro & Nanotechnol, Ctr Innovat Competence Macronano, D-98684 Ilmenau, Germany
[3] Atotech Deutsch GmbH, D-10553 Berlin, Germany
[4] Forschungszentrum Karlsruhe, Inst Microstruct Technol, D-76344 Eggenstein Leopoldshafen, Germany
[5] Forschungszentrum Karlsruhe, Inst Mat Res 3, D-76344 Eggenstein Leopoldshafen, Germany
[6] Forschungszentrum Karlsruhe, Inst Micro Proc Engn, D-76344 Eggenstein Leopoldshafen, Germany
[7] Draeger Med AG & Co KG, D-23542 Lubeck, Germany
[8] Forschungszentrum Karlsruhe, Inst Mat Res 1, D-76344 Eggenstein Leopoldshafen, Germany
[9] Leibniz Inst Plant Genet & crop Plant Res, In Vitro Differentiat Grp, D-06466 Gatersleben, Germany
关键词
D O I
10.1039/b618488j
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We describe a multi-purpose platform for the three-dimensional cultivation of tissues. The device is composed of polymer chips featuring a microstructured area of 1-2 cm(2). The chip is constructed either as a grid of micro-containers measuring 120-300 x 300 x 300 Pm (h x 1 x w), or as an array of round recesses (300 mu m diameter, 300 mu m deep). The micro-containers may be separately equipped with addressable 3D-micro-electrodes, which allow for electrical stimulation of excitable cells and on-site measurements of electrochemically accessible parameters. The system is applicable for the cultivation of high cell densities of up to 8 x 1 06 cells and, because of the rectangular grid layout, allows the automated microscopical analysis of cultivated cells. More than 1000 micro-containers enable the parallel analysis of different parameters under superfusion/perfusion conditions. Using different polymer chips in combination with various types of bioreactors we demonstrated the principal suitability of the chip-based bioreactor for tissue culture applications. Primary and established cell lines have been successfully cultivated and analysed for functional properties. When cells were cultured in non-perfused chips, over time a considerable degree of apoptosis could be observed indicating the need for an active perfusion. The system presented here has also been applied for the differentiation analysis of pluripotent embryonic stem cells and may be suitable for the analysis of the stem cell niche.
引用
收藏
页码:777 / 785
页数:9
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