Development of a new serum-free medium, USC-HC1, for growth and normal phenotype in postembryonic chicken growth plate chondrocytes
- PMID: 3771440
- DOI: 10.1007/BF02623519
Development of a new serum-free medium, USC-HC1, for growth and normal phenotype in postembryonic chicken growth plate chondrocytes
Abstract
A serum-free medium for postembryonic chicken epiphyseal growth plate chondrocytes has been developed from 104 MCDB medium. To enable these fastidious cells to survive, grow, and express normal phenotype, a substantial increase over MCDB 104 in the level of many of the amino acids was required, as well as a change in the buffer system and the addition of SerXtend, a defined, serum-free product containing various growth factors, including fibroblast growth factor. Also required was the provision of cell attachment factors, either by coating culture surfaces with type II collagen, or better, by allowing the freshly released cells to recover for several hours in a medium supplemented with 10% fetal bovine serum before plating. This new serum-free medium, which we call USC-HC1, supports growth and replication, the retention of normal polygonal morphology, the expression of significant levels of cellular alkaline phosphatase activity, the production of sulfated proteoglycans, type II collagen, and the formation of alkaline phosphatase-rich matrix vesicles by the chondrocytes. The major advantage of USC-HC1, however, is that it will provide for the first time an opportunity to examine the effects of various defined growth and hormonal factors on the phenotypic expression and differentiation of growth plate chondrocytes, in the absence of the variable (stimulatory and inhibitory) factors present in fetal bovine serum.
Similar articles
-
Development of a serum-free system to study the effect of growth hormone and insulinlike growth factor-I on cultured postembryonic growth plate chondrocytes.In Vitro Cell Dev Biol. 1992 Apr;28A(4):235-44. doi: 10.1007/BF02634239. In Vitro Cell Dev Biol. 1992. PMID: 1583002
-
Retinoic acid stimulates matrix calcification and initiates type I collagen synthesis in primary cultures of avian weight-bearing growth plate chondrocytes.J Cell Biochem. 1997 May;65(2):209-30. doi: 10.1002/(sici)1097-4644(199705)65:2<209::aid-jcb7>3.0.co;2-y. J Cell Biochem. 1997. PMID: 9136079
-
Effect of growth hormone, insulin-like growth factor I, basic fibroblast growth factor, and transforming growth factor beta on cell proliferation and proteoglycan synthesis by avian postembryonic growth plate chondrocytes.J Bone Miner Res. 1994 Mar;9(3):431-9. doi: 10.1002/jbmr.5650090320. J Bone Miner Res. 1994. PMID: 8191938
-
Effect of synthetic human parathyroid hormone on the levels of alkaline phosphatase activity and formation of alkaline phosphatase-rich matrix vesicles by primary cultures of chicken epiphyseal growth plate chondrocytes.Bone Miner. 1986 Oct;1(5):421-36. Bone Miner. 1986. PMID: 2462454
-
The use of avian epiphyseal chondrocytes for in vitro studies of skeletal metabolism.J Nutr. 1992 Mar;122(3 Suppl):802-5. doi: 10.1093/jn/122.suppl_3.802. J Nutr. 1992. PMID: 1542051 Review.
Cited by
-
Development of a serum-free system to study the effect of growth hormone and insulinlike growth factor-I on cultured postembryonic growth plate chondrocytes.In Vitro Cell Dev Biol. 1992 Apr;28A(4):235-44. doi: 10.1007/BF02634239. In Vitro Cell Dev Biol. 1992. PMID: 1583002
-
Interleukin-1 beta-modulated gene expression in immortalized human chondrocytes.J Clin Invest. 1994 Dec;94(6):2307-16. doi: 10.1172/JCI117595. J Clin Invest. 1994. PMID: 7989586 Free PMC article.
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Other Literature Sources
Miscellaneous