4.6 Article

Structure of pericellular matrix around agarose-embedded chondrocytes

Journal

OSTEOARTHRITIS AND CARTILAGE
Volume 15, Issue 10, Pages 1207-1216

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.joca.2007.03.023

Keywords

chondrocyte; pericellular matrix; tissue engineering; agarose

Funding

  1. NIAMS NIH HHS [AR33236] Funding Source: Medline
  2. NIBIB NIH HHS [R01 EB003805, EB003805] Funding Source: Medline

Ask authors/readers for more resources

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-e m bedded cells was initially much higher (similar to 400%) than that in chondrocytes within cartilage. Expression of col6 in the cultured chondrocytes declined by similar to 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. (C) 2007 Osteoarthritis Research Society International. Published by Elsevier Ltd. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available