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Identification of signaling mechanism of bone resorption and redox control in the aging mouse model

Research Project

Project/Area Number 23792526
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Social dentistry
Research InstitutionThe Nippon Dental University

Principal Investigator

OMATA Kazuhiko  日本歯科大学, 生命歯学部, 非常勤講師 (00434142)

Project Period (FY) 2011 – 2012
Project Status Completed (Fiscal Year 2012)
Budget Amount *help
¥3,770,000 (Direct Cost: ¥2,900,000、Indirect Cost: ¥870,000)
Fiscal Year 2012: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2011: ¥2,600,000 (Direct Cost: ¥2,000,000、Indirect Cost: ¥600,000)
Keywordsredox / 骨代謝 / 加齢 / 酸化ストレス
Research Abstract

In this study, we analyzed the molecular mechanism of bone metabolism due to aging changes, using the aging mouse-derived cells. We found that increased expression of redox-related molecules txnip decrease differentiation of osteoclast activity in vitro. The reduction of bone metabolic function due to aging, txnipmay regulate osteoclast genesis.

Report

(3 results)
  • 2012 Annual Research Report   Final Research Report ( PDF )
  • 2011 Research-status Report

URL: 

Published: 2011-08-05   Modified: 2025-11-18  

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