TY - JOUR
T1 - Osteogenesis in cultures of limb mesenchymal cells
AU - Osdoby, Philip
AU - Caplan, Arnold I.
N1 - Funding Information:
This work was supported by grants from the National Institutes of Health (No. DE-4006) and the National Foundation, March of Dimes, and by a training grant to Philip Osdoby from the National Institutes of Health (No. 5T32 GM 0722564). We are grateful to Dr. Bernard Tandler for critically reading this manuscript, and we acknowledge the expert technical assistance of Ms. Gail Cockrell and Ms. Katarina Riitich.
PY - 1979/11
Y1 - 1979/11
N2 - The results of previous reports demonstrated that osteoblasts develop in cultures derived from phenotypically unexpressive stage 24 chick limb mesenchymal cells. The observations reported here suggest that initial cell plating densities may provide environmental conditions deterministic to a particular limb phenotype. Quantitative microscopic studies, histochemical localization of calcium phosphate, and electron microscopy indicate that osteoblasts develop in cultures derived from stage 24 limb mesenchymal cells. Additionally, 1-3% of the cells from stage 24 limbs are associated with mineral deposits when plated at initial high densities (5 × 106 cells per 35-mm culture dish), while more than 50% of the cells are associated with cartilage by Day 9. Cultures plated at intermediate seeding densities (between 2.0 and 2.5 × 106 cells per 35-mm culture dish) have minimal cartilage development, and approximately 20% of the cells are associated with mineral by Day 9. Furthermore, cultures prepared from stage 31 limb mesenchymal cells form well-developed bone nodules with both osteoblasts and osteocytes present, but no cartilage. It is clear from these observations and from a consideration of the initiation of osteogenesisin vivo that the initiation of bone development in the limb is not associated with cartilage development. Based on these studies and observations on the effect of nutrient factors on phenotypic expression in culture, an hypothesis is presented relating differential vascularization and nutrient flow to the determination of limb phenotypesin vivo.
AB - The results of previous reports demonstrated that osteoblasts develop in cultures derived from phenotypically unexpressive stage 24 chick limb mesenchymal cells. The observations reported here suggest that initial cell plating densities may provide environmental conditions deterministic to a particular limb phenotype. Quantitative microscopic studies, histochemical localization of calcium phosphate, and electron microscopy indicate that osteoblasts develop in cultures derived from stage 24 limb mesenchymal cells. Additionally, 1-3% of the cells from stage 24 limbs are associated with mineral deposits when plated at initial high densities (5 × 106 cells per 35-mm culture dish), while more than 50% of the cells are associated with cartilage by Day 9. Cultures plated at intermediate seeding densities (between 2.0 and 2.5 × 106 cells per 35-mm culture dish) have minimal cartilage development, and approximately 20% of the cells are associated with mineral by Day 9. Furthermore, cultures prepared from stage 31 limb mesenchymal cells form well-developed bone nodules with both osteoblasts and osteocytes present, but no cartilage. It is clear from these observations and from a consideration of the initiation of osteogenesisin vivo that the initiation of bone development in the limb is not associated with cartilage development. Based on these studies and observations on the effect of nutrient factors on phenotypic expression in culture, an hypothesis is presented relating differential vascularization and nutrient flow to the determination of limb phenotypesin vivo.
UR - https://www.scopus.com/pages/publications/0018601476
U2 - 10.1016/0012-1606(79)90140-4
DO - 10.1016/0012-1606(79)90140-4
M3 - Article
C2 - 527770
AN - SCOPUS:0018601476
SN - 0012-1606
VL - 73
SP - 84
EP - 102
JO - Developmental Biology
JF - Developmental Biology
IS - 1
ER -