Recellularization of biological heart valves with human vascular cells: in vitro hemocompatibility assessment

J Biomed Mater Res B Appl Biomater. 2009 Jan;88(1):130-8. doi: 10.1002/jbm.b.31159.

Abstract

Coverage of cardiovascular bioprostheses with autologous endothelium is used for the purpose of improving blood compatibility. The aim of our study was to analyze endothelialization potential of glutaraldehyde-fixed heart valves, cellular functions of seeded endothelial cells (EC), and the impact of a two-stage seeding protocol using human vascular fibroblasts (FB) and EC from saphenous veins (HSVEC) on cellular functional properties in vitro. Adherence and morphology of adhered cells were assessed by scanning electronic microscopy and immunohistochemistry. Reproducible, complete surface coverage with EC was established on decellularized and glutaraldehyde-fixed bovine pericardium. Analyzing functional properties of cells directly adhered to biomaterial revealed nonproliferative cells, which were capable of inflammatory stimulation in terms of TNF-induced increase in interleukin-6 secretion and adhesion of inflammatory cells. Furthermore, EC showed sustained antithrombotic properties quantified by platelet adhesion onto EC and prostacyclin secretion by EC. Preseeding with vascular fibroblasts using a two-stage seeding protocol induced EC proliferation and improved inflammatory and anti-thrombotic functions. Cardiovascular biomaterials differ significantly in their potential to allow for adhesion of human EC. Successfully endothelialized biomaterial, however, revealed cellular properties which are likely to be favorable to improving performance of biomaterials. Two-stage seeding adds regenerative potential and improves cell functions of adherent EC.

MeSH terms

  • Animals
  • Biocompatible Materials / chemistry
  • Cattle
  • Cell Adhesion
  • Cell Proliferation
  • Endothelial Cells / cytology
  • Fibroblasts / metabolism*
  • Heart Valve Prosthesis*
  • Heart Valves / cytology*
  • Humans
  • Interleukin-6 / metabolism
  • Microscopy, Electron, Scanning
  • Pericardium / cytology
  • Tissue Engineering / methods*
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Biocompatible Materials
  • Interleukin-6
  • Tumor Necrosis Factor-alpha