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Abstract: During intramembranous bone formation,
preosteoblasts condense, differentiate into osteoblasts and
deposit bone matrix. We compared the differentiation process
of rat calvarial osteoblast-like cells inoculated as micromasses,
which mimic the in vivo condensation process, with cells inoculated
as monolayers. The cells were analysed morphologically at
1,2 and 3 weeks by light microscopy (alkaline phosphatase
activity, mineralization), by transmission electron microscopy,
and biochemically (collagen typing, alkaline phosphatase activity,
protein and DNA content). The cells inoculated as monolayers
formed alkaline phosphatase positive and mineralized nodules
during the culture period. The cells inoculated as a micromass
formed a large mineralized area consisting of smaller nodules.
The ultrastructure of the cells in both culture systems showed
the typical features of osteoblasts and osteocytes. The main
difference between monolayer and micromass cultures was found
after 1 week in culture. The cells inoculated as a micromass
formed a multilayer of cells. The cytoplasm contained rER,
mitochondria, vesicles and ribosomes. There were abundant
collagen fibrils in membrane folds and in the extracellular
matrix. This was in contrast to the cells in monolayer culture
which showed hardly any collagen fibrils in the extracellular
matrix. The promotion of the differentiation was also confirmed
by biochemical data showing that the DNA content was lower
in the micromass than in the monolayer cultures during the
culture period. These results show that micromass, as compared
to monolayer, culture promotes the differentiation of rat
osteoblast-like cells in vitro.
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