EFFECTS OF PROSTAGLANDIN-E(2) ON BONE-FORMATION IN CULTURED FETAL-RATCALVARIAE - ROLE OF INSULIN-LIKE GROWTH FACTOR-I

Citation
Lg. Raisz et al., EFFECTS OF PROSTAGLANDIN-E(2) ON BONE-FORMATION IN CULTURED FETAL-RATCALVARIAE - ROLE OF INSULIN-LIKE GROWTH FACTOR-I, Endocrinology, 133(4), 1993, pp. 1504-1510
Citations number
25
Categorie Soggetti
Endocrynology & Metabolism
Journal title
ISSN journal
00137227
Volume
133
Issue
4
Year of publication
1993
Pages
1504 - 1510
Database
ISI
SICI code
0013-7227(1993)133:4<1504:EOPOBI>2.0.ZU;2-F
Abstract
Prostaglandin E2 (PGE2) can stimulate collagen synthesis in bone at lo w concentrations or in the presence of cortisol. Moreover, cortisol in hibits and PGE2 stimulates the production of insulin-like growth facto r (IGF-I) in cultured osteoblastic cells. Therefore, we examined the r ole of IGF-I in the response to PGE2. In 96-h fetal rat calvarial orga n cultures, PGE2 increased, and cortisol and indomethacin decreased th e medium IGF-I concentration, suggesting that both exogenous and endog enous PGs regulate IGF-I production. In the presence of cortisol, the stimulatory effects of PGE2 on medium IGF-I and incorporation of [H-3] proline into collagenase-digestible protein were highly correlated (r = 0.95). When exogenous IGF-I (30 nM) was added, the stimulatory effe ct of PGE2 was abrogated in the absence, but not the presence, of cort isol. When we added IGF-binding proteins, which blocked the effects of IGF-I and IGF-II, collagenase-digestible protein labeling was decreas ed in control and cortisol-treated cultures, whereas the stimulatory e ffect of PGE2 was reduced, but not abrogated. We conclude that endogen ous IGFs play a role in maintaining bone formation in cultured fetal r at calvariae and may mediate in part the anabolic response to PGE2. Ho wever, the PGE2 response probably involves additional IGF-independent pathways.