Prostaglandin E (PGE)-induced morphological changes of osteoblasts and
its possible mechanisms mere investigated in cultured calvaria and is
olated osteoblasts from long bone fragments of neonatal rats. The cont
rol osteoblasts, either on the calvaria or isolated from the long bone
fragments, were flat, polygonal in shape, and arranged in a monolayer
under scanning electron microscopy (SEM) or phase contrast microscopy
. Treatment with 1 mu mol/L of prostaglandin E-2 (PGE(2), 2 h) caused
these bone cells to contract a soma, whereas 10 and 100 mu mol/L PGE(2
) (2 h) caused 18%-30% of the bone cells to elongate and expose the un
dersurface. Incubation of the cultured osteoblasts with PGE, at differ
ent time periods showed a bell-shaped pattern with the optimal respons
e at 2 h of incubation. A similar reaction can be induced by treatment
with prostaglandin E-1 (PGE(1)) or dibutyryl cyclic adenosine monopho
sphate (DBcAMP) in combination with 3-isobutyl-1-methylxanthine (IBMX)
. Furthermore, we assessed the percentage of responsive isolated bone
cells to investigate interactions with other agents. The morphological
changes induced by PGEs were inhibited by H-8, a protein kinase inhib
itor. On the other hand, elevated intracellular calcium enhanced the P
OE-induced morphological changes. Fluorescence labeling showed that PG
Es caused the breakdown of the actin microfilaments, but spared the mi
crotubules and vimentin filaments in the isolated osteoblast-like cell
s, These results suggest that the morphological changes of osteoblasts
induced by PGEs may be related to the intracellular cAMP and calcium
levels, (C) 1998 by Elsevier Science Inc. All rights reserved.