Prostaglandin (PG) E(2) displays physiological and pharmacological act
ion in various tissues including bone, It increases intracellular Ca,
and stimulates or inhibits cAMP production through the PGE receptor su
btypes EP(1), EP(2), and EP(3), respectively. These receptor subtypes
have been recently cloned. In the present study, we investigate the ex
pression of these receptor subtypes in bone tissue. RT-PCR revealed th
at EP(1), EP(2), and EP(3) were expressed in rat calvariae and that os
teoblastic cells (MC3T3-E1) expressed EP(1) and EP(2). In situ hybridi
zation analysis using cryosection of neonatal calvariae revealed that
EP(2) was expressed by osteoblasts and cells not in contact with bone,
probably including preosteoblasts. EP(2) expression was observed at a
n early stage in calvarial development, at 14 days prenatal. EP(2) exp
ression was also observed at day 3 in rat bone marrow cell culture in
which bone-like mineralized nodules are formed at day 8. It has been e
stablished that PGE(2) response accompanying cAMP production is one of
the characteristics of osteoblasts. The present results indicate that
this phenotype appears at an early stage of osteoblastic differentiat
ion and bone development.