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Establishment and application of in-vitro hypertrophic and degeneration model designed to clarify the mechanism of mechanical signal transduction in chondrocytes.

Establishment and application of in-vitro hypertrophic and degeneration model designed to clarify the mechanism of mechanical signal transduction in chondrocytes.
体外肥厚和变性模型的建立和应用旨在阐明软骨细胞机械信号转导机制。
批准号:
23659705
负责人:
CHIKUDA Hirotaka
金额:
$2.33万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Challenging Exploratory Research
财政年份:
2011
资助国家:
日本
项目状态:
已结题
起止时间:
2011 至 2012

项目摘要

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相关文献

中文摘要
翻译
本研究旨在建立体外软骨细胞肥大退变模型,以阐明软骨细胞机械信号转导的机制。通过对不同静水压力条件下软骨细胞退变标志物表达的检测,结果表明,20 Mpa压力1小时是诱导小鼠成软骨ATDC5细胞和小鼠原代关节软骨细胞退变的最佳刺激条件。
英文摘要
The purpose of this study is to establish in-vitro hypertrophic and degeneration model designed to clarify the mechanism of mechanical signal transduction in chondrocytes. The examination of expressions of degeneration markers of chondrocytes under various conditions of hydrostatic pressure revealed that pressure of 20MPa for 1 hour was the optimum stimulus condition to induce degenerative change in mouse chondrogenic ATDC5 cells and mouse primary articular chondrocytes.
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Research of Notch signal in pathophysiology and therapeutics of osteoarthritis
  • 批准号:
    23390358
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
  • 资助金额:
    $12.15万
  • 财政年份:
    2011
  • 负责人:
    CHIKUDA Hirotaka
  • 依托单位:
Molecular mechanisms of regulation in bone and cartilage metabolism by GSK3β
  • 批准号:
    20591775
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
  • 资助金额:
    $2.91万
  • 财政年份:
    2008
  • 负责人:
    CHIKUDA Hirotaka
  • 依托单位: