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Development of a novel human leukemia model using humanized mice

Development of a novel human leukemia model using humanized mice
使用人源化小鼠开发新型人类白血病模型
批准号:
24659487
负责人:
ISHII Naoto
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:
2012
资助国家:
日本
项目状态:
已结题
起止时间:
2012-04-01 至 2014-03-31

项目摘要

项目成果

ISHII Naoto的其他基金

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相关文献

中文摘要
翻译
将原发性人白血病细胞移植到免疫缺陷小鼠体内的体内研究,为我们了解人白血病的发病机制提供了重大进展。然而,在这些模型中,白血病细胞在移植到小鼠体内之前已经在人类患者体内发育,因此不适合研究生理性白血病的发生。因此,我们在这里开发了一种新的实验模型来分析白血病发生,在这种模型中,人类原代造血干细胞通过故意的基因撞击转化为白血病细胞。我们希望这一新建立的人源化小鼠模型将有助于未来的研究,旨在揭示白血病发生的分子机制和开发新的治疗白血病的方法。
英文摘要
In vivo studies in which primary human leukemia cells were transplanted into immunodeficient mice, provided significant advances in our understanding of the pathogenesis of human leukemia. However, these models, in which the leukemia cells had already developed in human patients before being transplanted into mice, are not suitable for studying physiological leukemogenesis. Therefore, we here developed a new experimental model for analyzing leukemogenesis in which primary human HSCs are converted into leukemia cells by deliberate genetic hits. We hope that this newly established model using humanized mice will contribute to future studies aimed at revealing the molecular mechanisms for leukemogenesis and developing new therapies against leukemia.
期刊论文(30)
专著(0)
科研奖励(0)
会议论文
Th17 cell generation and mucosal immunity
Th17细胞生成和粘膜免疫
DOI: --
发表时间: 2013
期刊:
影响因子: --
作者: [Takeshi Kawabe, Shu-lan Sun, Satoshi Yamaki, Atsuko Asao, Takeshi Takahashi, Takanori So, and Naoto Ishii]
通讯作者: and Naoto Ishii
L-arginine upregulates NO production by macrophages during infection with Leishmania major.
L-精氨酸在感染大型利什曼原虫期间上调巨噬细胞的 NO 产生。
DOI: --
发表时间: 2012
期刊:
影响因子: --
作者: [長島宏行, 山木聡史, Michael Croft, 石井直人, 宗孝紀, Atsuko Asaoほか]
通讯作者: Atsuko Asaoほか
DOI: 10.1371/journal.pone.0037892
发表时间: 2012
期刊: PloS one
影响因子: 3.7
作者: [Moriya K, Suzuki M, Watanabe Y, Takahashi T, Aoki Y, Uchiyama T, Kumaki S, Sasahara Y, Minegishi M, Kure S, Tsuchiya S, Sugamura K, Ishii N]
通讯作者: Ishii N
TRAF5 controls inflammatory CD4 T cells in experimental autoimmune encephalomyelitis
TRAF5 控制实验性自身免疫性脑脊髓炎中的炎症 CD4 T 细胞
DOI: --
发表时间: 2013
期刊:
影响因子: --
作者: [Nagashima H, Yamaki S, Asao A, Croft M, Ishii N, So T.]
通讯作者: So T.
共 17 条
    Roles for TNFR superfamily molecules in regulation of ILC function
    • 批准号:
      16K15508
    • 项目类别:
      Grant-in-Aid for Challenging Exploratory Research
    • 资助金额:
      $2.16万
    • 财政年份:
      2016
    • 负责人:
      ISHII Naoto
    • 依托单位:
    Identification and analysis of the niches for helper memory T cells
    • 批准号:
      15H04742
    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
      $10.98万
    • 财政年份:
      2015
    • 负责人:
      ISHII Naoto
    • 依托单位:
    Basic Research for the study and publication of materials in the collection of Mr. Natsuya Mitsuyoshi
    • 批准号:
      23520183
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $3.33万
    • 财政年份:
      2011
    • 负责人:
      ISHII Naoto
    • 依托单位:
    T-cell costimulation-mediated regulation of mucosal inflammation
    • 批准号:
      21390114
    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
      $11.9万
    • 财政年份:
      2009
    • 负责人:
      ISHII Naoto
    • 依托单位:
    海外基金