Depth-dependent biomechanical and biochemical properties of fetal, newborn, and tissue-engineered articular cartilage

J Biomech. 2007;40(1):182-90. doi: 10.1016/j.jbiomech.2005.11.002. Epub 2006 Jan 4.

Abstract

Adult articular cartilage has depth-dependent mechanical and biochemical properties which contribute to zone-specific functions. The compressive moduli of immature cartilage and tissue-engineered cartilage are known to be lower than those of adult cartilage. The objective of this study was to determine if such tissues exhibit depth-dependent compressive properties, and how these depth-varying properties were correlated with cell and matrix composition of the tissue. The compressive moduli of fetal and newborn bovine articular cartilage increased with depth (p<0.05) by a factor of 4-5 from the top 0.1 mm (28+/-13 kPa, 141+/-10 kPa, respectively) to 1 mm deep into the tissue. Likewise, the glycosaminoglycan and collagen content increased with depth (both p<0.001), and correlated with the modulus (both p<0.01). In contrast, tissue-engineered cartilage formed by either layering or mixing cells from the superficial and middle zone of articular cartilage exhibited similarly soft regions at both construct surfaces, as exemplified by large equilibrium strains. The properties of immature cartilage may provide a template for developing tissue-engineered cartilage which aims to repair cartilage defects by recapitulating the natural development and growth processes. These results suggest that while depth-dependent properties may be important to engineer into cartilage constructs, issues other than cell heterogeneity must be addressed to generate such tissues.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Animals, Newborn
  • Biomechanical Phenomena
  • Cartilage, Articular / embryology
  • Cartilage, Articular / growth & development
  • Cartilage, Articular / physiology*
  • Cattle
  • Collagen / metabolism
  • Compressive Strength
  • Female
  • Fetus / physiology
  • Glycosaminoglycans / metabolism
  • Pregnancy
  • Tissue Engineering

Substances

  • Glycosaminoglycans
  • Collagen