Effect of substrate mechanics on chondrocyte adhesion to modified alginate surfaces

Arch Biochem Biophys. 2004 Feb 15;422(2):161-7. doi: 10.1016/j.abb.2003.11.023.

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.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Alginates / chemistry*
  • 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 / cytology*
  • Chondrocytes / drug effects
  • Cross-Linking Reagents / chemistry
  • Cross-Linking Reagents / pharmacology
  • Cytochalasin D / pharmacology
  • Dose-Response Relationship, Drug
  • Kinetics
  • Microscopy, Electron, Scanning
  • Oligopeptides / chemistry*
  • Oligopeptides / pharmacology
  • Surface Properties

Substances

  • Alginates
  • Biocompatible Materials
  • Cross-Linking Reagents
  • Oligopeptides
  • Cytochalasin D
  • Barium
  • arginyl-glycyl-aspartic acid
  • Calcium