Endothelial cell adhesion on RGD-containing methacrylate terpolymers

J Biomed Mater Res A. 2004 Aug 1;70(2):265-73. doi: 10.1002/jbm.a.30074.

Abstract

Hexyl methacrylate (HMA), methyl methacrylate (MMA), and methacrylic acid (MAA) were used as comonomers to produce a low glass transition temperature material, potentially useful in fabricating a small diameter vascular graft. Because it has been shown that grafts seeded with endothelial cells have better resistance to thrombosis, RGD-based peptide sequences were incorporated into the terpolymer. The two methods used for incorporating peptide sequences were a chain transfer reaction during polymerization, and a coupling reaction between the amine terminus of the peptide and the carboxyl groups of the MAA. Polymers were synthesized using the chain transfer reaction with peptide concentrations ranging from 1.7 to 7.0 micromol/g. Weight-average molecular weights decreased with increasing peptide concentration from 310,000 g/mol for the terpolymer without peptide, to 110,000 g/mol for a peptide concentration of 7.0 micromol/g. As a result, Young's modulus decreased with increasing peptide concentration. Terpolymers with peptides attached through a coupling reaction showed no decrease in molecular weight or mechanical properties. Confocal microscopy showed cells seeded on the RGD surfaces adhered and spread, while terpolymers with RGE sequences showed cells that were rounded and not spreading. Cell density on RGD surfaces increased with increasing peptide concentration up to a bulk peptide concentration of approximately 5 micromol/g and reached a plateau, which indicated the minimum peptide concentration necessary for maximum cell adhesion.

Publication types

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

MeSH terms

  • Biocompatible Materials*
  • Biomechanical Phenomena
  • Bioprosthesis
  • Blood Vessel Prosthesis
  • Cell Adhesion
  • Cell Count
  • Cells, Cultured
  • Endothelium, Vascular / cytology*
  • Humans
  • Materials Testing
  • Oligopeptides*
  • Polymethacrylic Acids*
  • Surface Properties
  • Tissue Engineering

Substances

  • Biocompatible Materials
  • Oligopeptides
  • Polymethacrylic Acids
  • arginyl-glycyl-aspartic acid