Structure of pericellular matrix around agarose-embedded chondrocytes

Osteoarthritis Cartilage. 2007 Oct;15(10):1207-16. doi: 10.1016/j.joca.2007.03.023. Epub 2007 May 23.

Abstract

Objective: Determine whether the structure of the type VI collagen component of the chondrocyte pericellular matrix (PCM) generated by agarose-embedded chondrocytes in culture is similar to that found in native articular cartilage.

Methods: Confocal microscopy, quick-freeze deep-etch electron microscopy, and real-time polymerase chain reaction (PCR) were used to investigate temporal and spatial patterns of type VI collagen protein deposition and gene expression by bovine chondrocytes during 4 weeks of culture within a 2% agarose hydrogel. Similar analyses were performed on chondrocytes within samples of intact cartilage obtained from the same joint surfaces as those used for cell isolation for comparison.

Results: Type VI collagen accumulated uniformly around cells embedded in agarose, with the rate of deposition slowing after the second week. After 1 week, PCM fibrils were observed to be oriented perpendicular to the cell surface, in contrast with the primarily tangential fibrillar arrangement observed in native articular cartilage. Expression of col6 in agarose-embedded cells was initially much higher ( approximately 400%) than that in chondrocytes within cartilage. Expression of col6 in the cultured chondrocytes declined by approximately 60% after 1 week, and remained stable thereafter.

Conclusions: PCM structure and composition around cells in a hydrogel scaffold may be different than that in native cartilage, with potential implications for mass transport, mechanotransduction, and ultimately, the success of tissue engineering approaches.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Cartilage, Articular / cytology*
  • Cartilage, Articular / growth & development
  • Cartilage, Articular / physiology
  • Cattle
  • Cells, Cultured
  • Chondrocytes / cytology*
  • Chondrocytes / physiology
  • Chondrogenesis
  • Extracellular Matrix / physiology*
  • Extracellular Matrix / ultrastructure
  • Microscopy, Electron / methods
  • Polymerase Chain Reaction
  • Sepharose
  • Tissue Engineering / methods*

Substances

  • Sepharose