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The role of S1P3 signaling in the bone metabolism

Research Project

Project/Area Number 15K09533
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Collagenous pathology/Allergology
Research InstitutionKyoto Prefectural University of Medicine

Principal Investigator

KOHNO Masataka  京都府立医科大学, 医学(系)研究科(研究院), 講師 (60405256)

Co-Investigator(Kenkyū-buntansha) 川人 豊  京都府立医科大学, 医学(系)研究科(研究院), 准教授 (50336731)
中田 博  京都産業大学, 総合生命科学部, 教授 (90113141)
Project Period (FY) 2015-04-01 – 2018-03-31
Project Status Completed (Fiscal Year 2017)
Budget Amount *help
¥4,810,000 (Direct Cost: ¥3,700,000、Indirect Cost: ¥1,110,000)
Fiscal Year 2017: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
Fiscal Year 2016: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2015: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Keywordsスフィンゴシン1リン酸 / S1P3受容体 / S1P3-KOマウス / 骨粗しょう症 / 破骨細胞 / S1P3レセプター / スフィンゴシン1リン酸 / 骨粗鬆症 / マウス卵巣摘出骨粗鬆症モデル / スフィンゴシン1リン酸(S1P)
Outline of Final Research Achievements

The role of S1P3 receptor signaling in bone metabolism is poorly understood. Thus, we examined the mechanisms in the development of osteoporosis which were induced by ovariectomy in murine. pQCT showed that S1P3-/- (KO) mice had significantly lower bone mineral density compared with wild type (WT) in the 28 th day.
Osteoclast precursors obtained from femoral bone marrow were cultured for 7 days in the medium containing M-CSF. The adherent cells were resuspended and seeded on the culture plate coated with an inorganic crystalline calcium phosphate. These cells were cultured in the medium containing M-CSF and RANKL with or without variable concentration of S1P and area of absorption pits were cumulated and compared with each others. There was no significant differences of pit areas between WT and S1P3-KO in physiological concentrations(0, 0.1, 1microM) of S1P. It was suggested that S1P-S1P3 signaling in osteoclast didn't make a significant contribution to its activity.

Report

(4 results)
  • 2017 Annual Research Report   Final Research Report ( PDF )
  • 2016 Research-status Report
  • 2015 Research-status Report

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Published: 2015-04-16   Modified: 2019-03-29  

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