PMID- 21700269 OWN - NLM STAT- MEDLINE DCOM- 20120228 LR - 20161125 IS - 1879-1506 (Electronic) IS - 0003-9969 (Linking) VI - 56 IP - 11 DP - 2011 Nov TI - Effect of PGE(2) induced by compressive and tensile stresses on cementoblast differentiation in vitro. PG - 1238-46 LID - 10.1016/j.archoralbio.2011.05.007 [doi] AB - OBJECTIVE: The aim of the study was to clarify the mechanisms underlying orthodontically induced root resorption by characterizing the role of PGE(2) induced by compressive stress (CS) and tensile stress (TS) on cementoblast metabolism in vitro. DESIGN: Mouse cementoblast cell line OCCM-30 was continuously stimulated with 0.2 KPa CS or 5.0 KPa TS. COX-2 mRNA expression and PGE(2) production were thus quantified. In addition, cells were treated with COX-2 inhibitor and the role of PGE(2) induced by CS or TS on the expression of genes related to cementoblast differentiation was examined. PGE(2) receptors mRNA expression induced by CS or TS was also evaluated. Moreover, cells were treated with exogenous PGE(2) and the role of PGE(2) concentration on matrix mineralization was verified. RESULTS: CS and TS enhanced COX-2 mRNA expression and PGE(2) production. PGE(2) synthesis, however, was markedly induced by CS. Gene expression of bone morphogenetic protein 2 (BMP-2), osteocalcin (OCN) and receptor activator for nuclear factor kappaB ligand (RANKL) was enhanced by CS on an endogenous PGE(2)-mediated manner. Osteoprotegerin (OPG) expression was not affected by CS. Meanwhile, TS up-regulated the expression of BMP-2 and alkaline phosphatase (ALP) on an endogenous PGE(2)-mediated manner. TS down-regulated RANKL mRNA expression, whilst OPG expression was not affected. Moreover, EP4 mRNA expression was considerably enhanced by TS. Regarding PGE(2) concentration, only cells treated with low concentration presented anabolic response. CONCLUSIONS: Gene expression was differentially regulated according to the type of mechanical stimulation applied to cementoblasts. In addition, it is shown that PGE(2) plays an important role on mediating cementoblast mechanosensitivity. CI - Copyright (c) 2011 Elsevier Ltd. All rights reserved. FAU - Rego, Emanuel Braga AU - Rego EB AD - Department of Orthodontics and Craniofacial Developmental Biology, Hiroshima University Graduate School of Biomedical Sciences, 1-2-3 Kasumi, Minami-ku, Hiroshima 734-8553, Japan. emanuelbraga@hotmail.com FAU - Inubushi, Toshihiro AU - Inubushi T FAU - Kawazoe, Aki AU - Kawazoe A FAU - Miyauchi, Mutsumi AU - Miyauchi M FAU - Tanaka, Eiji AU - Tanaka E FAU - Takata, Takashi AU - Takata T FAU - Tanne, Kazuo AU - Tanne K LA - eng PT - Journal Article DEP - 20110622 PL - England TA - Arch Oral Biol JT - Archives of oral biology JID - 0116711 RN - 0 (Bone Morphogenetic Protein 2) RN - 0 (RANK Ligand) RN - 0 (Receptors, G-Protein-Coupled) RN - 104982-03-8 (Osteocalcin) RN - EC 1.14.99.1 (Cyclooxygenase 2) RN - K7Q1JQR04M (Dinoprostone) SB - IM MH - Animals MH - Bone Morphogenetic Protein 2/biosynthesis MH - Cell Differentiation/genetics MH - Cell Line, Transformed MH - Cementogenesis/*genetics MH - Cyclooxygenase 2/biosynthesis MH - Dental Cementum/*cytology/*metabolism/physiology MH - *Dental Stress Analysis MH - Dinoprostone/biosynthesis/*physiology MH - Gene Expression Regulation MH - *Mechanotransduction, Cellular MH - Mice MH - Mice, Transgenic MH - Osteocalcin/biosynthesis MH - Physical Stimulation MH - RANK Ligand/biosynthesis MH - Receptors, G-Protein-Coupled/biosynthesis/physiology MH - Root Resorption/etiology MH - Stress, Mechanical MH - Tooth Movement Techniques/adverse effects EDAT- 2011/06/28 06:00 MHDA- 2012/03/01 06:00 CRDT- 2011/06/25 06:00 PHST- 2011/01/14 00:00 [received] PHST- 2011/05/17 00:00 [revised] PHST- 2011/05/17 00:00 [accepted] PHST- 2011/06/25 06:00 [entrez] PHST- 2011/06/28 06:00 [pubmed] PHST- 2012/03/01 06:00 [medline] AID - S0003-9969(11)00161-0 [pii] AID - 10.1016/j.archoralbio.2011.05.007 [doi] PST - ppublish SO - Arch Oral Biol. 2011 Nov;56(11):1238-46. doi: 10.1016/j.archoralbio.2011.05.007. Epub 2011 Jun 22.