1. Effect of substrate mechanics on chondrocyte adhesion to modified alginate surfaces.
- Author
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Genes NG, Rowley JA, Mooney DJ, and Bonassar LJ
- Subjects
- Alginates pharmacology, Amino Acid Sequence, Animals, Barium chemistry, Biocompatible Materials chemistry, Biocompatible Materials pharmacology, Calcium chemistry, Cattle, Cell Adhesion drug effects, Cell Adhesion physiology, Chondrocytes drug effects, Cross-Linking Reagents chemistry, Cross-Linking Reagents pharmacology, Cytochalasin D pharmacology, Dose-Response Relationship, Drug, Kinetics, Microscopy, Electron, Scanning, Oligopeptides pharmacology, Surface Properties, Alginates chemistry, Chondrocytes cytology, Oligopeptides chemistry
- Abstract
This study characterized the attachment of chondrocytes to RGD-functionalized alginate by examining the effect of substrate stiffness on cell attachment and morphology. Bovine chondrocytes were added to wells coated with 2% alginate or RGD-alginate. The alginate was crosslinked with divalent cations ranging from 1.25 to 62.5 mmol/g alginate. Attachment to RGD-alginate was 10-20 times higher than attachment to unmodified alginate and was significantly inhibited by antibodies to integrin subunits alpha3l and beta1, cytochalasin-D, and soluble RGD peptide. The equilibrium level and rate of attachment increased with crosslink density and substrate stiffness. Substrate stiffness also regulated chondrocyte morphology, which changed from a rounded shape with nebulous actin on weaker substrates to a predominantly flat morphology with actin stress fibers on stiffer substrates. The dependence of attachment on integrins and substrate stiffness suggests that chondrocyte integrins may play a role in sensing the mechanical properties of the matrices to which they are attached.
- Published
- 2004
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