I. Sato , A. Suzuki , A. Kakita , Y. Ono , Y. Miura , M. Itoh , Y. Oiso
{"title":"Stimulatory effect of prostaglandin F2α on Na-dependent phosphate transport in osteoblast-like cells","authors":"I. Sato , A. Suzuki , A. Kakita , Y. Ono , Y. Miura , M. Itoh , Y. Oiso","doi":"10.1016/S0952-3278(03)00021-8","DOIUrl":null,"url":null,"abstract":"<div><div><span>Prostaglandin F</span><sub>2α</sub> (PGF<sub>2α</sub><span>) has been reported to activate protein kinase C (PKC) through both phospholipase (PL) C and D, resulting in the proliferation of osteoblast-like cells. In addition, it has also been reported that Erk mitogen-activated protein kinase is also involved in the mechanism of PGF</span><sub>2α</sub><span><span>-induced proliferation of these cells. Recently, we have reported that several growth factors stimulate Na-dependent phosphate transport (Pi transport) activity of osteoblast-like cells, which has been recognized to play an important role in their </span>mineralization. In the present study, we investigated the effect of PGF</span><sub>2α</sub> on Pi transport in MC3T3-E1 osteoblast-like cells. PGF<sub>2α</sub> stimulated Na-dependent Pi transport dose dependently in the range between 1<!--> <!-->nM and 10<!--> <!-->μM in MC3T3-E1 cells. The effect was time dependent up to 24<!--> <!-->h. Kinetic analysis revealed that PGF<sub>2α</sub><span><span><span> induces newly synthesized Pi transporter. Pretreatment with </span>actinomycin D and </span>cycloheximide suppressed PGF</span><sub>2α</sub><span>-induced enhancement of Pi transport. Combined effect of PMA and PGF</span><sub>2α</sub><span><span> was not additive in Pi transport. Calphostin C, a </span>PKC inhibitor, dose-dependently suppressed Pi transport induced by PGF</span><sub>2α</sub><span>. On the contrary, U0126, which inhibits an upstream kinase of Erk (MEK), did not affect PGF</span><sub>2α</sub>-induced enhancement of Pi transport.</div><div>In conclusion, PGF<sub>2α</sub> stimulates Pi transport through activation of PKC in osteoblast-like cells.</div></div>","PeriodicalId":94179,"journal":{"name":"Prostaglandins, leukotrienes, and essential fatty acids","volume":"68 5","pages":"Pages 311-315"},"PeriodicalIF":3.2000,"publicationDate":"2003-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Prostaglandins, leukotrienes, and essential fatty acids","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0952327803000218","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Prostaglandin F2α (PGF2α) has been reported to activate protein kinase C (PKC) through both phospholipase (PL) C and D, resulting in the proliferation of osteoblast-like cells. In addition, it has also been reported that Erk mitogen-activated protein kinase is also involved in the mechanism of PGF2α-induced proliferation of these cells. Recently, we have reported that several growth factors stimulate Na-dependent phosphate transport (Pi transport) activity of osteoblast-like cells, which has been recognized to play an important role in their mineralization. In the present study, we investigated the effect of PGF2α on Pi transport in MC3T3-E1 osteoblast-like cells. PGF2α stimulated Na-dependent Pi transport dose dependently in the range between 1 nM and 10 μM in MC3T3-E1 cells. The effect was time dependent up to 24 h. Kinetic analysis revealed that PGF2α induces newly synthesized Pi transporter. Pretreatment with actinomycin D and cycloheximide suppressed PGF2α-induced enhancement of Pi transport. Combined effect of PMA and PGF2α was not additive in Pi transport. Calphostin C, a PKC inhibitor, dose-dependently suppressed Pi transport induced by PGF2α. On the contrary, U0126, which inhibits an upstream kinase of Erk (MEK), did not affect PGF2α-induced enhancement of Pi transport.
In conclusion, PGF2α stimulates Pi transport through activation of PKC in osteoblast-like cells.