课题基金 / 基金详情

Osteogenic capacity of vascularized periosteal graft combined with cultured mesenchymal stem cells

Osteogenic capacity of vascularized periosteal graft combined with cultured mesenchymal stem cells
血管化骨膜移植物联合培养间充质干细胞的成骨能力
批准号:
13671535
负责人:
YAJIMA Hiroshi
金额:
$2.62万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
2001
资助国家:
日本
项目状态:
已结题
起止时间:
2001 至 2003

项目摘要

项目成果

YAJIMA Hiroshi的其他基金

相关文献

中文摘要
翻译
点击翻译按钮获取中文摘要
英文摘要
The purpose of our study was to analyze the osteogenic capacity of the vascularized * using an experimental model of the vascularized tibial periosteum and various cerai * in rats. In addition, we investigate the efficacy of cultured mesenchymal stem cells ******* vascularized periosteal graft model as well.Hydroxyapatite or β TCP as a scaffold was wrapped with the vascularized perio * composite was grafted under skin of thigh area. Marked bone formation was observed in both hydroxyapatite and β TCP group at 2 weeks or later. However, in the vascularized fascia-ceramics composite group (control group), no bone formation was observed histologically. Biochemical analysis using alkaline phosphatase and osteocalsin also indicate the same results. On the other hand, from in vitrostudy of osteoinduction by collagen apatite composite combined with cultured MSCs, osteoinduction potential of the collagen apatite composite with MSCs group was significantly higher than apatite only group as a control. Based on the results of our previous series, we performed in vivo study using vascularized periosteal graft model combined with cultured MSCs in mature rats. A collagen apatite composite was selected as the scaffold. In MSCs impregnated group, much more bone formation was observed than non-MSCs group. In conclusion, even in the matured rat which has little potential of osteogenesis, combained method of vascularized periosteum and cultured MSCs has high osteogenic capacity. And so we consider this combined method must be useful in the treatment of refractory non-union of the bones in human.
期刊论文(2)
专著(0)
科研奖励(0)
会议论文
T.Noshi, T.Yoshikawa et al.: "Recombinant human bone morphogenetic protein-2 potentates the in vivo osteogenic ability of marrow/hydroxyapatite composites"Artif Organs. 25(3). 201-208 (2001)
T.Noshi、T.Yoshikawa 等人:“重组人骨形态发生蛋白-2 增强骨髓/羟基磷灰石复合材料的体内成骨能力”Artif Organs。
DOI: --
发表时间:
期刊:
影响因子: --
作者: []
通讯作者:
T.Yoshikawa.et al.: "Osteogenic Activity of FK506-Treated Cultured Bone Tissue"Bioceramics. 14. 391-394
T.Yoshikawa.等人:“FK506处理的培养骨组织的成骨活性”生物陶瓷。
DOI: --
发表时间:
期刊:
影响因子: --
作者: []
通讯作者:
Role of the relation between morphology and function of sensory neuron in the development and evolution of sensory architecture
  • 批准号:
    25460251
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
  • 资助金额:
    $3.24万
  • 财政年份:
    2013
  • 负责人:
    YAJIMA Hiroshi
  • 依托单位:
Development os remoto consultation system using collective intelligence
  • 批准号:
    24500243
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
  • 资助金额:
    $2.83万
  • 财政年份:
    2012
  • 负责人:
    YAJIMA Hiroshi
  • 依托单位:
Mechanisms underlying evolutionary architecture of primary sensory neurons in chordates
  • 批准号:
    23790234
  • 项目类别:
    Grant-in-Aid for Young Scientists (B)
  • 资助金额:
    $2.83万
  • 财政年份:
    2011
  • 负责人:
    YAJIMA Hiroshi
  • 依托单位:
Molecular basis for acquisition of de novo sensory circuit
  • 批准号:
    21790189
  • 项目类别:
    Grant-in-Aid for Young Scientists (B)
  • 资助金额:
    $2.75万
  • 财政年份:
    2009
  • 负责人:
    YAJIMA Hiroshi
  • 依托单位: