ATDC5 cells were employed to examine how inorganic phosphate (Pi) influence
s chondrocytic bone formation. 1) Pi (3 - 30 mM) plus ascorbic acid (50 mug
/ml) dose-dependently accelerated proliferative differentiation and mineral
ization of ATDC5. 2) Northern blot analysis revealed that 10 mM Pi suppress
ed expression of type II collagen and PTH (parathyroid hormone) / PTH-relat
ed peptide (PTHrP) receptor, while it accelerated type X collagen expressio
n. 3) Pi (3 - 30 mM) dose-dependently increased luciferase activity in the
cells transfected with 3000 bp type X collagen promoter fused to the lucife
rase gene. The results suggest a regulatory role of Pi in endochondral oste
ogenesis.