Chondrogenic potential of in vitro multiplied rabbit perichondrium cells cultured in alginate beads in defined medium

Citation
Gjvm. Van Osch et al., Chondrogenic potential of in vitro multiplied rabbit perichondrium cells cultured in alginate beads in defined medium, TISSUE ENG, 6(4), 2000, pp. 321-330
Citations number
38
Categorie Soggetti
Cell & Developmental Biology
Journal title
TISSUE ENGINEERING
ISSN journal
10763279 → ACNP
Volume
6
Issue
4
Year of publication
2000
Pages
321 - 330
Database
ISI
SICI code
1076-3279(200008)6:4<321:CPOIVM>2.0.ZU;2-V
Abstract
Perichondrium has a chondrogenic capacity and is therefore a candidate tiss ue for engineering of cartilage in vitro. Donor age and culture conditions probably influence chondrogenesis. The aim of this study was to compare the chondrogenic capacity of ear and nasal perichondrium from young and adult rabbits, using serum containing and serum-free culture conditions. This stu dy demonstrates that more than 1 million cells can be generated out of 1 cm (2) of perichondrium tissue in 3-5 weeks of culture, irrespective of age. C ulturing of these cells in alginate in medium with 2, 10, or 20% fetal calf serum did result in the production of small amounts of glycosaminoglycan, but no collagen type II was demonstrated. When serum was replaced however b y insulin-like growth factor-1 (IGF-1) (10 ng/mL) plus transforming growth factor-beta 2 (TGF-beta 2) (10 ng/mL) an increased glycosaminoglycan produc tion and induction of collagen type II was found, especially in cells isola ted from perichondrium of the ear. Cells derived from perichondrium of youn g rabbits showed larger chondrogenic potential than cells from perichondriu m of adult rabbits. Moreover, stimulation of both glycosaminoglycan synthes is and collagen type II production was about five times higher in cells iso lated from the ear perichondrium of young rabbits than of adult rabbits. We conclude that young auricular perichondrium seems a useful source of cells for tissue engineering of cartilage when cultured in serum-free medium in combination with IG-F1 and TGF-beta 2.