Asymmetrical seeding of MSCs into fibrin-poly(ester-urethane) scaffolds and its effect on mechanically induced chondrogenesis

J Tissue Eng Regen Med. 2017 Oct;11(10):2912-2921. doi: 10.1002/term.2194. Epub 2016 Jul 13.

Abstract

Mesenchymal stem cells (MSCs) are currently being investigated as candidate cells for regenerative medicine approaches for the repair of damaged articular cartilage. For these cells to be used clinically, it is important to understand how they will react to the complex loading environment of a joint in vivo. In addition to investigating alternative cell sources, it is also important for the structure of tissue-engineered constructs and the organization of cells within them to be developed and, if possible, improved. A custom built bioreactor was used to expose human MSCs to a combination of shear and compression loading. The MSCs were either evenly distributed throughout fibrin-poly(ester-urethane) scaffolds or asymmetrically seeded with a small proportion seeded on the surface of the scaffold. The effect of cell distribution on the production and deposition of cartilage-like matrix in response to mechanical load mimicking in vivo joint loading was then investigated. The results show that asymmetrically seeding the scaffold led to markedly improved tissue development based on histologically detectable matrix deposition. Consideration of cell location, therefore, is an important aspect in the development of regenerative medicine approaches for cartilage repair. This is particularly relevant when considering the natural biomechanical environment of the joint in vivo and patient rehabilitation protocols. Copyright © 2016 John Wiley & Sons, Ltd.

Keywords: bioreactor; cartilage repair; mesenchymal stem cell; multi-axial load; poly-ester-urethane; shear.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Aged
  • Chondrogenesis / drug effects*
  • DNA / metabolism
  • Female
  • Fibrin / pharmacology*
  • Fluorescent Dyes / metabolism
  • Gene Expression Regulation / drug effects
  • Glycosaminoglycans / metabolism
  • Humans
  • Image Processing, Computer-Assisted
  • Immunohistochemistry
  • Male
  • Mesenchymal Stem Cells / cytology*
  • Mesenchymal Stem Cells / drug effects
  • Mesenchymal Stem Cells / metabolism
  • Middle Aged
  • Polyesters / pharmacology*
  • Polyurethanes / pharmacology*
  • Staining and Labeling
  • Tissue Scaffolds / chemistry*
  • Young Adult

Substances

  • Fluorescent Dyes
  • Glycosaminoglycans
  • Polyesters
  • Polyurethanes
  • microthane foam
  • Fibrin
  • DNA