Basic fibroblast growth factor (bFGF) inhibited osteoclast-like cell f
ormation in co-cultures of mouse bone marrow cells either with the mou
se stromal cell line, ST2, or with primary osteoblastic cells. Basic F
GF significantly inhibited the osteoclast-like cell formation, induced
by 1 alpha,25-dihydroxyvitamin D-3[1 alpha,25(OH)(2)D-3] when the cyt
okine was added to the culture, at an intermediate stage, suggesting t
hat bFGF inhibits the differentiation of the osteoclast progenitors. W
ith regard to target cells, bFGF directly affected ST2; it increased [
H-3]thymidine uptake and decreased the number of alkaline phosphatase-
positive cells. In contrast, bFGF had no inhibitory effect on the colo
ny formation of bone marrow cells induced by macrophage colony stimula
ting factor in methylcellulose culture. In addition, ST2 cells treated
with bFGF produced similar amounts of colony forming activity to thos
e without the cytokine. These findings indicated that the bFGF is not
involved in the proliferation of progenitor cells even in the presence
of ST2 cells. Furthermore, bFGF inhibited osteoclast-like cell format
ion induced not only by 1 alpha,25(OH)(2)D-3, but also by prostaglandi
n E(2) and by interleukin-11. These results suggest that bFGF inhibits
the common site of osteoclast-like cell formation, as induced by diff
erent mechanisms. Our data also indicated that the target cells for bF
GF in inhibiting osteoclast formation are not osteoclast progenitors b
ut stromal cells such as ST2 and osteoblastic cells, which support ost
eoclast development. (C) 1996 Wiley-Liss, Inc.