Sphingomyelin regulates blood glucose levels by bone tissue
Project/Area Number |
26463202
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Social dentistry
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Research Institution | Osaka Dental University |
Principal Investigator |
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Co-Investigator(Kenkyū-buntansha) |
池尾 隆 大阪歯科大学, 歯学部, 教授 (40159603)
岡崎 俊朗 金沢医科大学, 医学部, 教授 (40233308)
吉澤 達也 熊本大学, 大学院生命科学研究部(医), 准教授 (40313530)
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Project Period (FY) |
2014-04-01 – 2017-03-31
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Project Status |
Completed (Fiscal Year 2016)
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Budget Amount *help |
¥4,940,000 (Direct Cost: ¥3,800,000、Indirect Cost: ¥1,140,000)
Fiscal Year 2016: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2015: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2014: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
|
Keywords | 骨代謝 / 骨芽細胞 / スフィンゴミエリン合成酵素 / 骨芽細胞分化 / 破骨細胞分化因子 / 破骨細胞 / 糖代謝 |
Outline of Final Research Achievements |
The skeleton has been shown recently to regulate glucose metabolism through an osteoblast-specific hormone. Here, we investigated the role of sphingomyelin in osteoblasts. Knockdown of sphingomyelin synthase 1 or 2 resulted in inhibited osteoblast differentiation and reduced osteoclast formation. We found that sphingomyelin synthase affected osteoblast function, and we suggested sphingomyelin synthase effects to regulate glucose metabolism by osteoblast.
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Report
(4 results)
Research Products
(4 results)
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[Journal Article] RNA interference-mediated knockdown of Smad1 inhibits receptor activator of nuclear factor κB ligand expression induced by BMP-2 in primary osteoblasts.2015
Author(s)
Yoshikawa Y, Yoshizawa T, Domae E, Hieda Y, Takeyama A, Hirota S, Kawamoto A, Goda S, Tamura I, Kamada A, Komasa Y, Morita S, Yamagata K, Ikeo T.
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Journal Title
Archives of Oral Biology
Volume: 60
Issue: 9
Pages: 1319-26
DOI
Related Report
Peer Reviewed / Acknowledgement Compliant
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