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Mechanisms of cartilage growth: Modulation of balance between proteoglycan and collagen in vitro using chondroitinase ABC

✍ Scribed by Anna Asanbaeva; Koichi Masuda; Eugene J.-M. A. Thonar; Stephen M. Klisch; Robert L. Sah


Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
256 KB
Volume
56
Category
Article
ISSN
0004-3591

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✦ Synopsis


Abstract

Objective

To examine the cartilage growth–associated effects of a disruption in the balance between the swelling pressure of glycosaminoglycans (GAGs) and the restraining function of the collagen network, by diminishing GAG content prior to culture using enzymatic treatment with chondroitinase ABC.

Methods

Immature bovine articular cartilage explants from the superficial and middle layers were analyzed immediately or after incubation in serum‐supplemented medium for 13 days. Other explants were treated with chondroitinase ABC to deplete tissue GAG and also either analyzed immediately or after incubation in serum‐supplemented medium for 13 days. Treatment‐ and incubation‐associated variations in tissue volume, contents of proteoglycan and collagen network components, and tensile mechanical properties were assessed.

Results

Incubation in serum‐supplemented medium resulted in expansive growth with a marked increase in tissue volume that was associated with a diminution of tensile integrity. In contrast, chondroitinase ABC treatment on day 0 led to a marked reduction of GAG content and enhancement of tensile integrity, and subsequent incubation led to maturational growth with minimal changes in tissue volume and maintenance of tensile integrity at the enhanced levels.

Conclusion

The data demonstrate that a manipulation of GAG content in articular cartilage explants can distinctly alter the growth phenotype of cartilage. This may have practical utility for tissue engineering and cartilage repair. For example, the expansive growth phenotype may be useful to fill cartilage defects, while the maturational growth phenotype may be useful to induce matrix stabilization after filling defect spaces.