The role of heme oxygenase-1 in mechanical stress- and lipopolysaccharide-induced osteogenic differentiation in human periodontal ligament cells

被引:27
作者
Cho, Jin-Hyoung [3 ]
Lee, Sun-Kyung [1 ]
Lee, Jin-Woo [2 ]
Kim, Eun-Cheol [1 ]
机构
[1] Wonkwang Univ, Coll Dent, Dept Oral & Maxillofacial Pathol, Iksan 570749, Jeonbuk, South Korea
[2] Dankook Univ, Coll Dent, Dept Orthodont, Cheonan, South Korea
[3] Wonkwang Univ, Coll Dent, Dept Orthodont, Iksan 570749, Jeonbuk, South Korea
关键词
Mechanical stress; LPS; Osteogenic differentiation; HO-1; PDLCs; MESENCHYMAL STEM-CELLS; BONE MORPHOGENETIC PROTEIN-2; HUMAN PULP CELLS; PROINFLAMMATORY CYTOKINES; ORTHODONTIC ATTACHMENTS; INFLAMMATORY CYTOKINES; RECEPTOR ACTIVATOR; GINGIVAL HEALTH; TENSILE STRAIN; IN-VITRO;
D O I
10.2319/091509-520.1
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objective: To investigate the mechanisms through which mechanical stress and lipopolysaccharide treatment modulate osteoblastic differentiation in periodontal ligament cells. Materials and Methods: Cells were treated with lipopolysaccharide and/or mechanical strain applied with a Flexercell Strain Unit. Protein expression and mRNA were analyzed by Western blotting and reverse transcription polymerase chain reaction, respectively. Results: When lipopolysaccharide was co-applied with mechanical strain, the increase in the expression of bone morphogenetic protein-2, bone morphogenetic protein-7, and Runx2 mRNA seen with mechanical strain alone was restricted, but heme oxygenase-1 expression was further enhanced. Furthermore, pretreatment with an inhibitor of heme oxygenase-1 or inhibitors of p38, mitogen-activated protein kinase, JNK, phosphoinositide 3-kinases, protein kinase G, and nuclear factor kappa B restricted osteogenic differentiation induced by the application of lipopolysaccharide and mechanical strain. Conclusions: These results suggest that orthodontic force-induced osteogenesis in alveolar bone is inhibited by the accompanying periodontal inflammation via the upregulation of heme oxygenase-1 expression. Thus, the heme oxygenase-1 pathway could provide a possible therapeutic strategy to improve bone formation in orthodontic treatment. (Angle Orthod. 2010;80:740-747.)
引用
收藏
页码:740 / 747
页数:8
相关论文
共 34 条
  • [1] Akamatsu Yorihiro, 2004, FASEB J, V18, P771
  • [3] Cell differentiation by mechanical stress
    Altman, GH
    Horan, RL
    Martin, I
    Farhadi, J
    Stark, PRH
    Volloch, V
    Richmond, JC
    Vunjak-Novakovic, G
    Kaplan, DL
    [J]. FASEB JOURNAL, 2001, 15 (14) : 270 - +
  • [4] A cytoprotective role for the heme oxygenase-1/CO pathway during neural differentiation of human mesenchymal stem cells
    Barbagallo, Ignazio
    Tibullo, Daniele
    Di Rosa, Michelino
    Giallongo, Cesarina
    Palumbo, Giuseppe A.
    Raciti, Giuseppina
    Campisi, Agata
    Vanella, Angelo
    Green, Colin J.
    Motterlini, Roberto
    [J]. JOURNAL OF NEUROSCIENCE RESEARCH, 2008, 86 (09) : 1927 - 1935
  • [5] Bone morphogenetic proteins, their antagonists, and the skeleton
    Canalis, E
    Economides, AN
    Gazzerro, E
    [J]. ENDOCRINE REVIEWS, 2003, 24 (02) : 218 - 235
  • [6] Cytoskeletal changes and the system of regulation of alkaline phosphatase activity in human periodontal ligament cells induced by mechanical stress
    Chiba, M
    Mitani, H
    [J]. CELL BIOCHEMISTRY AND FUNCTION, 2004, 22 (04) : 249 - 256
  • [7] Osf2/Cbfa1: A transcriptional activator of osteoblast differentiation
    Ducy, P
    Zhang, R
    Geoffroy, V
    Ridall, AL
    Karsenty, G
    [J]. CELL, 1997, 89 (05) : 747 - 754
  • [8] Estes BT, 2004, CURR TOP DEV BIOL, V60, P91
  • [9] Establishing and characterizing human periodontal ligament fibroblasts immortalized by SV40T-antigen and hTERT gene transfer
    Fujii, S
    Maeda, H
    Wada, N
    Kano, Y
    Akamine, A
    [J]. CELL AND TISSUE RESEARCH, 2006, 324 (01) : 117 - 125
  • [10] Effects of cyclic compressive loading on chondrogenesis of rabbit bone-marrow derived mesenchymal stem cells
    Huang, CYC
    Hagar, KL
    Frost, LE
    Sun, YB
    Cheung, HS
    [J]. STEM CELLS, 2004, 22 (03) : 313 - 323