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J. Biol. Chem., Vol. 259, Issue 11, 6766-6772, 06, 1984
JH Glaser and HE Conrad
Chick embryo tibial chondrocyte growth and activities were compared in
serum-free and serum-supplemented media. A basal salts medium containing
equal volumes of Ham's F-12 and Dulbecco's modified Eagle's medium was
supplemented with 10% fetal calf serum or with a mixture of bovine insulin,
transferrin, fibroblast growth factor, dexamethasone, a prostaglandin E1
supplement, and a liposome supplement. Chondrocytes grew at identical rates
in both media. Insulin, liposomes, and fibroblast growth factor were
required for optimum growth in the serum- free medium, but removal of
transferrin, dexamethasone, or prostaglandin E1 had little effect on the
growth rate. In the serum- supplemented medium, the chondrocytes
synthesized Type II collagen, Mr = 59,000 collagen, and both the large,
cartilage-specific and the small ubiquitous proteochondroitin SO4 species
typically produced by cultured chondrocytes. In the serum-free medium there
was a shift toward synthesis of Type I collagen and a loss of the capacity
to synthesize Mr = 59,000 collagen and the cartilage-specific
proteochondroitin SO4. The loss of capacity for cartilage-specific
proteochondroitin SO4 synthesis began immediately after replacement of the
serum with the mixture of defined growth factors and the rate of loss was
retarded but not reversed when serum was added back in place of the growth
factors. When the serum and the mixture of growth factors were added
together to the basal medium at the time of cell plating, the chondrocytes
grew rapidly and retained their normal phenotype observed in serum-
supplemented cultures. Thus, the serum appears to contain factors which are
required for retention of the chondrocyte phenotype in culture over and
above those factors necessary for cell growth.
Properties of chick embryo chondrocytes grown in serum-free medium
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