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Controlling cell interactions by micropatterning in co-cultures: Hepatocytes and 3T3 fibroblasts

539

Citations

35

References

1997

Year

TLDR

In vitro tissue repair strategies manipulate cell environments via ECM, cell–cell, or soluble cues, but precise control of cell–cell interactions in multi‑cell co‑cultures has been limited; microfabrication offers spatial control yet has not been applied to simultaneous co‑cultivation of multiple cell types. The authors aimed to develop a versatile micropatterning method for two distinct cell types to precisely control their interactions. The method uses aminosilane‑linked biomolecules for surface modification combined with serum content manipulation to pattern the cells. The technique enabled precise control of homotypic and heterotypic contacts without altering cell numbers, demonstrating tunable cell–cell interactions across a wide range. © 1997 John Wiley & Sons, Inc.

Abstract

The repair or replacement of damaged tissues using in vitro strategies has focused on manipulation of the cell environment by modulation of cell-extracellular matrix interactions, cell-cell interactions, or soluble stimuli. Many of these environmental influences are easily controlled using macroscopic techniques; however, in co-culture systems with two or more cell types, cell-cell interactions have been difficult to manipulate precisely using similar methods. Although microfabrication has been widely utilized for the spatial control of cells in culture, these methods have never been adapted to the simultaneous co-cultivation of more than one cell type. We have developed a versatile technique for micropatterning of two different cell types based on existing strategies for surface modification with aminosilanes linked to biomolecules and the manipulation of serum content of cell culture media. This co-culture technique allowed manipulation of the initial cellular microenvironment without variation of cell number. Specifically, we were able to control the level of homotypic interaction in cultures of a single cell type and the degree of heterotypic contact in co-cultures over a wide range. This methodology has potential applications in tissue engineering, implant biology, and developmental biology, both in the arena of basic science and optimization of function for technological applications. © 1997 John Wiley & Sons, Inc.

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