Issue 6, 2007

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

Abstract

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 cm2. The chip is constructed either as a grid of micro-containers measuring 120–300 × 300 × 300 µm (h × l × w), or as an array of round recesses (300 µm diameter, 300 µm 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 × 106 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.

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

Article information

Article type
Paper
Submitted
18 Dec 2006
Accepted
27 Mar 2007
First published
16 Apr 2007

Lab Chip, 2007,7, 777-785

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

E. Gottwald, S. Giselbrecht, C. Augspurger, B. Lahni, N. Dambrowsky, R. Truckenmüller, V. Piotter, T. Gietzelt, O. Wendt, W. Pfleging, A. Welle, A. Rolletschek, A. M. Wobus and K. Weibezahn, Lab Chip, 2007, 7, 777 DOI: 10.1039/B618488J

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