Biotin-conjugated anti-CD44 antibody-avidin binding system for the improvement of chondrocyte adhesion to scaffolds

J Biomed Mater Res A. 2014 Apr;102(4):1140-8. doi: 10.1002/jbm.a.34770. Epub 2013 Jul 19.

Abstract

The clinical need for improved treatment options for patients with cartilage injuries has motivated tissue-engineering studies aimed at the in vitro generation of cell-based implants with functional properties. The success of tissue-engineered repair of cartilage may depend on the rapid and efficient adhesion of transplanted cells to the scaffold. In the present study, chondrocyte-scaffold constructs were engineered by planting porcine chondrocytes into nonporous chitosan membranes and 3D porous chitosan scaffolds that were treated with or without biotin-conjugated anti-CD44 antibody-avidin binding system and avidin-biotin binding system. The spreading area, cell exfoliation rates, cell proliferation rates, histological analysis, DNA and glycosaminoglycan (GAG) content, and mRNA expression were investigated to evaluate the efficiency of biotin-conjugated anti-CD44 antibody-avidin binding system for the improvement of cell adhesion to scaffolds in the cartilage tissue. The results showed that the biotin-conjugated anti-CD44 antibody-avidin binding system improved cell adhesion to scaffolds effectively. These studies suggest that this binding system has the potential to provide improved tissue-engineered cartilage for clinical applications.

Keywords: anti-CD44 antibody; avidin-biotin; cartilage tissue engineering; cell adhesion; chondrocytes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies / metabolism*
  • Avidin
  • Biotin / metabolism*
  • Cartilage / metabolism
  • Cell Adhesion
  • Cell Movement
  • Cell Proliferation
  • Cells, Cultured
  • Chondrocytes / cytology*
  • Chondrocytes / metabolism*
  • DNA / metabolism
  • Gene Expression Regulation
  • Glycosaminoglycans / metabolism
  • Hyaluronan Receptors / metabolism*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Staining and Labeling
  • Sus scrofa
  • Time Factors
  • Tissue Engineering
  • Tissue Scaffolds / chemistry*

Substances

  • Antibodies
  • Glycosaminoglycans
  • Hyaluronan Receptors
  • RNA, Messenger
  • Avidin
  • Biotin
  • DNA