Effect of RAGE on the interaction between osteoblasts and osteoclasts and its epigenetic regulation
Project/Area Number |
22590999
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Metabolomics
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Research Institution | Chiba University |
Principal Investigator |
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Co-Investigator(Kenkyū-buntansha) |
TATSUNO Ichiro 東邦大学, 医療センター佐倉病院, 教授 (80282490)
TANAKA Tomoaki 千葉大学, 大学院・医学研究院, 講師 (50447299)
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Project Period (FY) |
2010 – 2012
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Project Status |
Completed (Fiscal Year 2012)
|
Budget Amount *help |
¥4,420,000 (Direct Cost: ¥3,400,000、Indirect Cost: ¥1,020,000)
Fiscal Year 2012: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2011: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2010: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
|
Keywords | 糖尿病 / シグナル伝達 / エピジェネティクス / 骨リモデリング / 破骨細胞 |
Research Abstract |
The receptor for AGEs (RAGE) is implicated in the progression of diabetic complications. We were interested in determining the influence of RAGE on bone metabolism. In the experiments using pre-osteoclastic RAW264.7 cells and pre-osteoblastic MC3T3-E1 cells, ligand-induced activation of RAGE-stimulates osteoclastogenesis through factors secreted from osteoblasts. Each NFATc1-downstream gene has a different timing of its peak expression, suggesting stage-specific regulation of the each NFATc1 target genes.
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Report
(4 results)
Research Products
(25 results)
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[Presentation] 骨粗鬆症の診断と治療2011
Author(s)
吉田知彦
Organizer
千葉メディカルセンターベイサイドフォーラム
Place of Presentation
オークラ千葉ホテル、千葉(招待講演)
Year and Date
2011-11-25
Related Report
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