Research Article

Extrahepatic 25-Hydroxylation of Vitamin D3 in an Engineered Osteoblast Precursor Cell Line Exploring the Influence on Cellular Proliferation and Matrix Maturation during Bone Development

Figure 4

Absolute proliferation of MC3T3-E1 cells maintained in six types of tissue culture medium in duplicates over three two-week periods and assayed in duplicates ( ). Two types of media were used, one with osteogenic factors (BM+) and one without (BM−). At day 5, the MC3T3-E1 cell counts in the wells containing vitamin D metabolites ± osteogenic factor were statistically lower than the negative control (BM−). At day 10, the OPC1 cell counts in the wells containing vitamin D metabolites ± osteogenic factors (BM+) were also statistically lower ( ) then than the negative control (BM−) and remained at around 50% of the BM− cellular confluency. MC3T3-E1 cells treated with BM+ and vitamin D3 were indistinguishable from 1,25OH2D3 in that both experienced the largest statistically ( ) antiproliferative effect. Means ± SEM are shown with linear trendlines in the same color scheme for each experimental group.
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