Cr. Lee et al., Articular cartilage chondrocytes in type I and type II collagen-GAG matrices exhibit contractile behavior in vitro, TISSUE ENG, 6(5), 2000, pp. 555-565
Natural healing of articular cartilage defects generally does not occur, an
d untreated lesions may predispose the joint to osteoarthritis. To promote
healing of cartilage defects, many researchers are turning toward a tissue
engineering approach involving cultured cells and/or porous, resorbable mat
rices. This study investigated the contractile behavior of cultured canine
chondrocytes seeded in a porous collagen-glycosaminoglycan (GAG) scaffold.
Chondrocytes isolated from the knee joints of adult canines and expanded in
monolayer culture were seeded into porous collagen-GAG scaffolds. Scaffold
s were of two different compositions, with the predominant collagen being e
ither type I or type TI collagen, and of varying pore diameters, Over the 4
-week culture period, the seeded cells contracted all of the type I and typ
e II collagen-based matrices, despite a wide range of stiffness (145 +/- 23
Pa, for the type I scaffold, to 732 +/- 35 Pa, for the type II material).
Pore diameter (25-85 mum, type I; and 53-257 mum, type II) did not affect c
ell-mediated contraction. Immunohistochemical staining revealed the presenc
e of alpha -smooth muscle actin, an isoform responsible for contraction of
smooth muscle cells and myofibroblasts, in the cytoplasm of the seeded cell
s and in chondrocytes in normal adult canine articular cartilage.