Cyclical tensile force on periodontal ligament cells inhibits osteoclastogenesis through OPG induction

被引:70
作者
Kanzaki, H
Chiba, M
Sato, A
Miyagawa, A
Arai, K
Nukatsuka, S
Mitani, H
机构
[1] Tohoku Univ, Grad Sch Dent, Div Orthodont & Dentfacial Orthoped, Aoba Ku, Sendai, Miyagi 9808575, Japan
[2] Tohoku Univ, Grad Sch Dent, Dept Oral Hlth & Dev Sci, Div Oral Dysfunct Sci,Aoba Ku, Sendai, Miyagi 9808575, Japan
关键词
osteoprotegerin (OPG); TGF-beta; occlusal force; tensile force; osteoclastogenesis;
D O I
10.1177/154405910608500512
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
The periodontal ligament (PDL) maintains homeostasis of periodontal tissue under mechanical tensile-loading caused by mastication. Occlusal load inhibits atrophic alveolar bone resorption. Previously, we discovered that continuous compressive force on PDL cells induced osteoclastogenesis-supporting activity, with up-regulation of RANKL. We hypothesized that, unlike compression, cyclical tensile force upregulates OPG expression in PDL cells via TGFbeta up-regulation, and does not induce osteoclastogenesis-supporting activity. PDL cells were mechanically stimulated by cyclical tensile force in vitro. The conditioned media of PDL cells that had been subjected to cyclical tensile force inhibited osteoclastogenesis. Cyclical tensile force up-regulated not only RANKL mRNA expression, but also OPG mRNA expression in PDL cells. Tensile force up-regulated TGF-beta expression in PDL cells as well. Administration of neutralizing antibodies to TGF-beta inhibited OPG upregulation under cyclical tensile-force stimulation in a dose-dependent manner. Additionally, the osteoclastogenesis-inhibitory effect of the conditioned media of PDL cells under cyclical tensile force was partially rescued by the administration of TGF-beta neutralizing antibodies. In conclusion, tensile force inhibited the osteoclastogenesis-supporting activity of PDL cells by inducing the up-regulation of OPG via TGF-beta stimulation.
引用
收藏
页码:457 / 462
页数:6
相关论文
共 31 条
[1]   Osteoblast-like properties of human periodontal ligament cells: an in vitro analysis [J].
Basdra, EK ;
Komposch, G .
EUROPEAN JOURNAL OF ORTHODONTICS, 1997, 19 (06) :615-621
[2]  
BELLOWS CG, 1982, J CELL SCI, V58, P125
[3]   TRANSFORMING GROWTH FACTOR-BETA INHIBITS FORMATION OF OSTEOCLAST-LIKE CELLS IN LONG-TERM HUMAN MARROW CULTURES [J].
CHENU, C ;
PFEILSCHIFTER, J ;
MUNDY, GR ;
ROODMAN, GD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (15) :5683-5687
[4]  
COHN S. A., 1965, ARCH ORAL BIOL, V10, P909, DOI 10.1016/0003-9969(65)90084-1
[6]  
DAVIDOVITCH Z, 1988, DENT CLIN N AM, V32, P411
[7]   The roles of osteoprotegerin and osteoprotegerin ligand in the paracrine regulation of bone resorption [J].
Hofbauer, LC ;
Khosla, S ;
Dunstan, CR ;
Lacey, DL ;
Boyle, WJ ;
Riggs, BL .
JOURNAL OF BONE AND MINERAL RESEARCH, 2000, 15 (01) :2-12
[8]   Control of osteoclastogenesis and bone resorption by members of the TNF family of receptors and ligands [J].
Horowitz, MC ;
Xi, YG ;
Wilson, K ;
Kacena, MA .
CYTOKINE & GROWTH FACTOR REVIEWS, 2001, 12 (01) :9-18
[9]   Transforming growth factor-β induces expression of receptor activator of NF-κB ligand in vascular endothelial cells derived from bone [J].
Ishida, A ;
Fujita, N ;
Kitazawa, R ;
Tsuruo, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (29) :26217-26224
[10]   Serum inhibitors for human mast cell growth: possible role of retinol [J].
Ishida, S ;
Kinoshita, T ;
Sugawara, N ;
Yamashita, T ;
Koike, K .
ALLERGY, 2003, 58 (10) :1044-1052