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Analysis of dendritic cells after intra-bone marrow bone marrow transplantation

Analysis of dendritic cells after intra-bone marrow bone marrow transplantation
骨髓内骨髓移植后树突状细胞分析
批准号:
17590362
负责人:
INABA Muneo
金额:
$2.24万
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:
2005
资助国家:
日本
项目状态:
已结题
起止时间:
2005 至 2006

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中文摘要
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英文摘要
Long-term repopulating ability (LTRA) of hemopoietic stem cells (HSCs) has been assessed by serial bone marrow transplantation (BMT), and using this protocol, we provide evidence that intra-bone marrow BMT (IBM-BMT) can efficiently reconstitute the hemopoietic system with cells of donor origin, in contrast to conventional intravenous bone marrow transplantation (IV- BMT). The frequency of donor-derived progenitor cells having Lin^-/c-kit^+ phenotype or more primitive progenitors with immunophenotype of CD34^+/Sca-1^+ cells is higher in the recipients that had received bone marrow cells (BMCs) by IBM-BMT in the tertiary recipients than those received BMCs by IV-BMT. Furthermore, neither donor-derived progenitor cells nor mature hematolymphoid cells were detected in 〜25% of the tertiary recipients that had received BMCs by IV-BMT, indicating that progenitor cells can be efficiently maintained by IBM-BMT, but not IV- BMT. This was confirmed by the comparison of the progenitor cells between the recipients that had received BMCs by IBM-BMT or IV-BMT one year previously. In addition to these findings, conventional and plasmacytoid dendritic cells (cDCs and pDCs respectively) were normally differentiated even in the tertiary recipients by IBM-BMT, but not by IV-BMT. These findings clearly show that IBM-BMT is suitable for long-term maintenance of the hematolymphoid system of donor origin.
期刊论文(16)
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DOI: 10.1016/j.vetimm.2006.07.002
发表时间: 2006-11-15
期刊: VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY
影响因子: 1.8
作者: [Wijewardana, Viskam, Sugiura, Kikuya, Inaba, Toshio]
通讯作者: Inaba, Toshio
Treatment of streptozotocin-induced diabetes mellitus in rats by transplantation of islet cells from two MHC-disparate rats in combination with intra-bone marrow infection of allogeneic bone marrow cells.
通过移植来自两只 MHC 不同大鼠的胰岛细胞并结合同种异体骨髓细胞的骨髓内感染来治疗链脲佐菌素诱导的大鼠糖尿病。
DOI: --
发表时间: 2005
期刊: Transplantation 79
影响因子: --
作者: [Taira, M.]
通讯作者: M.
Bone marrow transplantation as a strategy for the treatment of autoimmune hearing loss in MRL/Mp-lpr/lpr mice
骨髓移植作为治疗 MRL/Mp-lpr/lpr 小鼠自身免疫性听力损失的策略
DOI: --
发表时间:
期刊: J Neuroimmunol in press
影响因子: --
作者: [Iwai H, et al.]
通讯作者: et al.
Comparative immunobiology of thymic DC mRNA in autoimmune-prone mice
自身免疫易感小鼠胸腺 DC mRNA 的比较免疫生物学
DOI: --
发表时间: 2007
期刊: Journal of Autoimmunity 28
影响因子: --
作者: [Okada, T.]
通讯作者: T.
12
    Study in the effects of IBM-BMT using parabiotic mice
    • 批准号:
      20590413
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $3.0万
    • 财政年份:
      2008
    • 负责人:
      INABA Muneo
    • 依托单位:
    Treatment of autoimmune diseases by portal venous bone marrow transplantation
    • 批准号:
      12670219
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $2.18万
    • 财政年份:
      2000
    • 负责人:
      INABA Muneo
    • 依托单位:
    Studies on the B cell development and its microenvironment
    • 批准号:
      08670264
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $1.6万
    • 财政年份:
      1996
    • 负责人:
      INABA Muneo
    • 依托单位:
    Studies on Characterization and function of thymic B cells.
    • 批准号:
      01570277
    • 项目类别:
      Grant-in-Aid for General Scientific Research (C)
    • 资助金额:
      $1.41万
    • 财政年份:
      1989
    • 负责人:
      INABA Muneo
    • 依托单位:
    国内基金
    海外基金
    树突状细胞(Dendritic cells,DCs)介导的黏膜免疫对猪轮状病毒(PRV)感染的分子作用机制研究
    • 批准号:
      31272541
    • 项目类别:
      面上项目
    • 资助金额:
      82.0万元
    • 批准年份:
      2012
    • 负责人:
      王春凤
    • 依托单位: