Dedifferentiation of chondrocytes remains a major problem in cartilage tissue
engineering. The development of hydrogels that can preserve chondrogenic
phenotype and prevent chondrocyte dedifferentiation is a meaningful strategy to
solve dedifferentiation problem of chondrocytes. In the present study, three
gels were prepared (alginate gel (Alg gel), type I collagen gel (Col gel), and
their combination gel (Alg/Col gel)), and the in vitro efficacy of chondrocytes
culture while preserving their phenotypes was investigated. While Col gel became
substantially contracted with time, the cells encapsulated in Alg gel preserved
the shape over the culture period of 14 days. The mechanical and cell-associated
contraction behaviors of Alg/Col gel were similar to those of Alg. The cells in
Alg and Alg/Col gels exhibited round morphology, whereas those in Col gel became
elongated (i.e. fibroblast-like) during cultures. The cells proliferated with
time in all gels with the highest proliferation being attained in Col gel. The
expression of chondrogenic genes, including SOX9, type II
collagen, and aggrecan, was significantly up-regulated in Alg/Col gel and Col
gel, particularly in Col gel. However, the chondrocyte dedifferentiation
markers, type I collagen and alkaline phosphatase (ALP), were
also expressed at significant levels in Col gel, which being contrasted with the
events in Alg and Alg/Col gels. The current results suggest the cells cultured
in hydrogels can express chondrocyte dedifferentiation markers as well as
chondrocyte markers, which draws attention to choose proper hydrogels for
chondrocyte-based cartilage tissue engineering.