• Search Research Projects
  • Search Researchers
  • How to Use
  1. Back to previous page

Regulation of pathologic root resorption by control of MAPK signaling

Research Project

Project/Area Number 15592169
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Orthodontic/Pediatric dentistry
Research InstitutionNagasaki University

Principal Investigator

HOTOKEZAKA Hitoshi  Nagasaki University, Graduate School of Biomedical Science, Assistant Professor, 大学院・医歯薬学総合研究科, 講師 (90199513)

Co-Investigator(Kenkyū-buntansha) KITAMURA Akira  Nagasaki University, Graduate School of Biomedical Science, Associate Professor, 大学院・医歯薬学総合研究科, 助教授 (30094767)
NEMOTO Takayuki  Nagasaki University, Graduate School of Biomedical Science, Professor, 大学院・医歯薬学総合研究科, 教授 (90164665)
NAKAYAMA Koji  Nagasaki University, Graduate School of Biomedical Science, Professor, 大学院・医歯薬学総合研究科, 教授 (80150473)
Project Period (FY) 2003 – 2004
Project Status Completed (Fiscal Year 2004)
Budget Amount *help
¥3,500,000 (Direct Cost: ¥3,500,000)
Fiscal Year 2004: ¥1,400,000 (Direct Cost: ¥1,400,000)
Fiscal Year 2003: ¥2,100,000 (Direct Cost: ¥2,100,000)
Keywordsodontoclasts / osteoclasts / root resorption / MAPK / MEK / ERK / p38 / RANKL / differentiation
Research Abstract

Root resorption sometimes occurs by orthodontic treatment, tooth dislocation, ooclusal interference, reimplantation of tooth, and it is one of big problems in dental treatment. The causative cells are odontoclasts that is basically thought as osteoclasts. In order to investigate the effect of MAPK signaling in root resorption, bone marrow macrophage was cultured in the presence of M-CSF and RANKL on calcium phosphate-coated plate. In this in vitro culture system, MAPK inhibitors were added to see the effect. After fixation and TRAP staining, the number of osteoclasts and pit formation were counted. In the presence of MEK/ERK inhibitors, increase of osteoclast number was observed. On the other hand, p38MAPK suppressed osteoclastogenesis. Then, MEK,ERK,and p38(wild type form and constitutive active form) were transfected into the cell of the culture system. However, the difference was not observed. Then, the time effect of MAPK inhibitors in the osteoclastogenesis was investigated. P38MAPK inhibitor SB203580 inhibited osteoclastogenesis in the early stage of differentiation, and it had no effect in the late stage of osteoclastognesis. Furthermore, in the late stage of osteoclastogenesis, not only RANKL but also other proinflammatory factors such as TNF-alpha, lipopolysaccharide induced fusion of osteoclasts, which implies periodontal inflammation factors enhance root resorption during chronic inflammatory circumstances caused by orthodontic treatment and occlusal trauma

Report

(3 results)
  • 2004 Annual Research Report   Final Research Report Summary
  • 2003 Annual Research Report
  • Research Products

    (6 results)

All 2004 2003 Other

All Journal Article (5 results) Publications (1 results)

  • [Journal Article] Infection-induced upregulation of the costimulatory molecule 4-1BB in osteoblastic cells and its inhibitory effect on M-CSF/RANKL-induced in vitro osteoclastogenesis2004

    • Author(s)
      Saito K, Ohara N, Hotokezaka H, Fukumoto S, Yuasa K, Naito M, Fujiwara T, Nakayama K.
    • Journal Title

      The Journal of Biological Chemistry 279

      Pages: 13555-13563

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2004 Final Research Report Summary
  • [Journal Article] Infection-induced upregulation of the costimulatory molecule 4-1BB in osteoblastic cells and its inhibitory effect on M-CSF/RANKL-induced in vitro osteoclastogenesis.2004

    • Author(s)
      Saito K, Ohara N, Hotokezaka H, Fukumoto S, Yuasa K, Naito M, Fujiwara T, Nakayama K.
    • Journal Title

      The Journal of Biological Chemistry 279

      Pages: 13555-13563

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2004 Final Research Report Summary
  • [Journal Article] Infection-induced upregulation of the constimulatory molecule 4-1BB in osteoblastic cells and its inhibitory effect on M-CSF/RANKL-induced in vitro osteoclastogenesis2004

    • Author(s)
      Saito, K.
    • Journal Title

      The Journal of Biological Chemistry 279

      Pages: 13555-13563

    • Related Report
      2004 Annual Research Report
  • [Journal Article] Interleukin-4 directly inhibits tumor necrosis factor-alpha-mediated osteoclast formation in mouse bone marrow macrophages2003

    • Author(s)
      Kitaura H, Nagata N, Fujimura Y, Hotokezaka H, Tatamiya M, Nakao N, Yoshida N, Nakayama K.
    • Journal Title

      Immunology Letters 8

      Pages: 193-198

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2004 Final Research Report Summary
  • [Journal Article] Interleukin-r4 directly inhibits tumor necrosis factor-alpha-mediated osteoclast formation in mouse bone marrow macrophages2003

    • Author(s)
      Kitaura H, Nagata N, Fujimura Y, Hotokezaka H, Tatamiya M, Nakao N, Yoshida N, Nakayama K.
    • Journal Title

      Immunology Letters 8

      Pages: 193-198

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2004 Final Research Report Summary
  • [Publications] Saito, K.: "Infection-induced upregulation of the costimulatory molecule 4-1BB in osteoblastic cells and its inhibitory effect on M-CSF/RANKL-induced in vitro osteoclastogenesis"The Journal of Biological Chemistry. 印刷中. (2004)

    • Related Report
      2003 Annual Research Report

URL: 

Published: 2003-04-01   Modified: 2016-04-21  

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi