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

基本信息

  • 批准号:
    17590362
  • 负责人:
  • 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
  • 起止时间:
    2005 至 2006
  • 项目状态:
    已结题

项目摘要

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.
造血干细胞(HSC)的长期再增殖能力(LTRA)已通过连续骨髓移植(BMT)进行了评估,并且使用该方案,我们提供了证据表明,与传统的静脉内骨髓移植(IV-BMT)相比,骨髓内BMT(IBM-BMT)可以有效地用供体来源的细胞重建造血系统 骨髓移植)。在三级受者中,通过 IBM-BMT 接受骨髓细胞 (BMC) 的受者中,具有 Lin^-/c-kit^+ 表型或具有 CD34^+/Sca-1^+ 细胞免疫表型的更原始祖细胞的频率高于通过 IV-BMT 接受 BMC 的受者。此外,在通过 IV-BMT 接受 BMC 的约 25% 的三级受者中,既没有检测到供体来源的祖细胞,也没有检测到成熟的血淋巴细胞,这表明 IBM-BMT 可以有效维持祖细胞,但 IV-BMT 则不行。通过对一年前通过 IBM-BMT 或 IV-BMT 接受 BMC 的接受者之间的祖细胞进行比较证实了这一点。除了这些发现之外,即使在第三代受者中,常规树突状细胞和浆细胞样树突状细胞(分别为 cDC 和 pDC)也可以通过 IBM-BMT 正常分化,但通过 IV-BMT 则不能。这些发现清楚地表明IBM-BMT适合长期维持供体来源的血淋巴系统。

项目成果

期刊论文数量(16)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Generation of canine dendritic cells from peripheral blood monocytes without using purified cytokines
  • DOI:
    10.1016/j.vetimm.2006.07.002
  • 发表时间:
    2006-11-15
  • 期刊:
  • 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:
  • 影响因子:
    0
  • 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
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
Prevention of graft-veusus host disease by intra-bone marrow injection of donor T cells
骨髓内注射供体 T 细胞预防移植物宿主病
  • DOI:
  • 发表时间:
    2007
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Fukui;J.
  • 通讯作者:
    J.
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INABA Muneo其他文献

INABA Muneo的其他文献

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{{ truncateString('INABA Muneo', 18)}}的其他基金

Study in the effects of IBM-BMT using parabiotic mice
使用联体小鼠研究 IBM-BMT 的效果
  • 批准号:
    20590413
  • 财政年份:
    2008
  • 资助金额:
    $ 2.24万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Treatment of autoimmune diseases by portal venous bone marrow transplantation
门静脉骨髓移植治疗自身免疫性疾病
  • 批准号:
    12670219
  • 财政年份:
    2000
  • 资助金额:
    $ 2.24万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Studies on the B cell development and its microenvironment
B细胞发育及其微环境的研究
  • 批准号:
    08670264
  • 财政年份:
    1996
  • 资助金额:
    $ 2.24万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Studies on Characterization and function of thymic B cells.
胸腺B细胞的特性和功能研究。
  • 批准号:
    01570277
  • 财政年份:
    1989
  • 资助金额:
    $ 2.24万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (C)

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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:
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迁移树突状细胞对胸腺中肿瘤特异性 T 细胞命运的影响
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