Influence of Glass and Polymer Coatings on Cho Cell Morphology and Adhesion.
From: BioChip Laboratory-CEA, 17 rue des Martyrs, 38054 Grenoble cedex 9, France.
Biomaterials
- Publish Date: Mar 2007
- ISSN: 0142-9612
- Volume: 28
- Issue: 8
- Pages: 1572-84
- Medium: Print
- Language: English
- Citation (JAMA): Sordel Thomas, Kermarec-Marcel Frederique, Garnier-Raveaud Stephanie, et al. Influence of Glass and Polymer Coatings on Cho Cell Morphology and Adhesion.. Biomaterials Mar 2007;28:1572-84
Abstract
Successful development of cell-on-chip microsystems where living cells are deposited and grown in microfabricated structures is highly dependent on the control of cell/substrate interactions. In this study, several materials of interest were tested for CHO cell growth and morphology: (i) glass, fibronectin-, poly-L-lysine- and 3-aminopropyltriethoxysilane (APTES) — treated glass and UV/O(3)-modified PDMS coating on glass as well as (ii) silicon, poly-L-lysine-, APTES-, O(2) plasma-treated and oxide-coated silicon. In addition, we quantitatively characterized cell adhesion to these substrates using a radial flow detachment assay. Lack of correlation between cell adhesion and cell morphology was systematically observed for all substrates. In particular, we show that PDMS coatings on glass can be finely tuned by UV/O(3) treatment to enhance cell adhesion and induce elongated morphology. Moreover, we observed a low shear stress cell detachment mechanism on silicon oxide coatings on silicon wafers. It is therefore possible with these coatings to selectively influence either cell adhesion or morphology.
Mesh Headings (Keywords): Animals, CHO Cells, Cell Adhesion, Coated Materials, Biocompatible, Cricetinae, Cricetulus, Glass, Polymers, Silicon
Check for Full Text / PubMed Unique Identifier (PMID): 17140656
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