INHIBITORY EFFECT OF IPRIFLAVONE ON OSTEOCLAST-MEDIATED BONE-RESORPTION AND NEW OSTEOCLAST FORMATION IN LONG-TERM CULTURES OF MOUSE UNFRACTIONATED BONE-CELLS
K. Notoya et al., INHIBITORY EFFECT OF IPRIFLAVONE ON OSTEOCLAST-MEDIATED BONE-RESORPTION AND NEW OSTEOCLAST FORMATION IN LONG-TERM CULTURES OF MOUSE UNFRACTIONATED BONE-CELLS, Calcified tissue international, 53(3), 1993, pp. 206-209
To study the effect of ipriflavone on osteoclast-mediated bone resorpt
ion and new osteoclast formation, we used an unfractionated bone cell
culture system containing mature osteoclasts from femur and tibia of n
ewborn mice. Ipriflavone (10(-5) M) inhibited pit formation on dentin
slices and caused a decrease in the number of tartrate-resistant acid
phosphatase (TRAP)-positive (+) multinucleate cells (MNCs) in a 4-day
culture period in which no increase in the number of TRAP(+)-MNCs was
observed in the presence of 5% fetal bovine serum (FBS) and 10(-8) M 1
alpha,25-dihydroxyvitamin D3 (1alpha,25(OH)2D3). During the following
12 days, both the total area of the pits and the number of TRAP(+)-MNC
s increased in the control. Continuous treatment with ipriflavone also
inhibited the increase in pit area during this period. These effects
of ipriflavone were reversible. Furthermore, the differentiation of os
teoclasts was examined when preexisting TRAP(+)-MNCs were removed by i
ncubation in the absence of 1alpha,25(OH)2D3 for the initial 4 days in
culture dishes without dentin slices. When 1alpha,25(OH)2D3 and iprif
lavone were added to the medium on the 4th day, ipriflavone inhibited
new TRAP(+)-MNC formation stimulated by 1alpha,25(OH)2D3 in a dose-dep
endent manner. However, pre-treatment of the cells with ipriflavone be
fore the addition of 1alpha,25(OH)2D3 did not inhibit TRAP(+)-MNC form
ation. These results indicate that ipriflavone inhibits both the activ
ation of mature osteoclasts and the formation of new osteoclasts witho
ut affecting growth of TRAP-negative progenitor cells.