Developemtnt, Prfuction, and promotion of usilization of Mast Cell Deficient W/W/^v and Sl/Sl^d Mice.

肥大细胞缺陷型 W/W/^v 和 Sl/Sl^d 小鼠的发育、生产和利用促进。

基本信息

  • 批准号:
    60880010
  • 负责人:
  • 金额:
    $ 8.64万
  • 依托单位:
  • 依托单位国家:
    日本
  • 项目类别:
    Grant-in-Aid for Developmental Scientific Research
  • 财政年份:
    1985
  • 资助国家:
    日本
  • 起止时间:
    1985 至 1987
  • 项目状态:
    已结题

项目摘要

Genetically mast cell-deficient W/W^v and Sl/Sl^d mice are useful for the analysis of mast cell biology. Especially, W/W^v mine are useful as recipients of bone marrow cells and skin pieces. Inasmuch as suspentsion and clonal cultures of mast cells have been developed, wwe combined these in vivio and in vitro systems.1) Suspension-cultured mast cells had morphological and biochemical characteristics similar to those of mucosla mast cells (MMX). However, i.p. injection of such cultured mast cells bage rise to development of cells charactersitics similar to those of nonnective tissue mast cells (CTMC).2) Hwen peritoneal cells of normal +/+ mice were cultured in methylcellulose, pure mast cell colonies appeared. Cells from individual mast cell colonies were divided and injected into the skin and stomach W/W^v mice; CTMC developed in the skin and MMC in the stomach mucosa. This indicates the presence of a common precursor for CTMC and MMC.3) Morphology of such bipotent mast cell precustors was studied by using micromanipultaion About 4% of morphologically identifiable peritineal mast cells may function as the bipotent precursors,4) Although W/W^v mice showed a defect in resistance against ixodid ticks, injection of suspension-cultured mast cells normalized the defect. The examples mentioned above indicate that combinations if in vivo and in vitro systems increara the usedfulness of W/W^v mice.
遗传性肥大细胞缺陷的W/W^v和Sl/Sl^d小鼠可用于肥大细胞生物学分析。特别是,W/W/V矿物质可用作骨髓细胞和皮肤片的受体。由于肥大细胞的悬浮培养和克隆培养已经发展成熟,我们将它们在体内和体外系统中结合起来。1)悬浮培养的肥大细胞具有与粘膜肥大细胞(MMX)相似的形态学和生化特征。2)将正常+/+小鼠腹腔细胞培养于甲基纤维素中,可形成纯肥大细胞集落。将来自单个肥大细胞集落的细胞分裂并注射到W/W^v小鼠的皮肤和胃中; CTMC在皮肤中发育,MMC在胃粘膜中发育。这表明CTMC和MMC的共同前体的存在。3)通过显微操作研究这种双能肥大细胞前体的形态。大约4%的形态可鉴定的腹膜肥大细胞可能起双能前体的作用。4)尽管W/W_v小鼠对硬蜱的抵抗力存在缺陷,但注射悬浮培养的肥大细胞使缺陷正常化。上述实施例表明,体内和体外系统的组合增加了W/W +/-小鼠的可用性。

项目成果

期刊论文数量(197)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Journal of Parasitology. 71-443. (1985)
寄生虫学杂志。
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    0
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Kanakura,Y.: American Journal of Pathology. 127. 191-198 (1987)
Kanakura,Y.:美国病理学杂志。
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    0
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Kawaguchi-Nagata,K.: Journal of Biochemestry. 103. 24-30 (1988)
川口永田,K.:生物化学杂志。
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    0
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  • 通讯作者:
Kitamura,Y.In Kakunaga,T.,Sugimura,T.,Tomatis,L.and Yamazaki,H. eds.: "Unique features in differentiation of mast cells.Cell Differetiation, Genes and Cancer" IARC,Lyon, (IN PRESS)
Kitamura,Y.In Kakunaga,T.,Sugimura,T.,Tomatis,L.和Yamazaki,H.
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    0
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  • 通讯作者:
Galli, S. J.: "Animal model of human disease: genetically mast cell-deficient W/W^v and Sl/Sl^d mice. Their value for analysis of roles of mast cells in biologic responses in ivivo." Ametical Journal of Parhology. 127. 191-198 (1987)
Galli, S. J.:“人类疾病的动物模型:遗传上肥大细胞缺陷的 W/W^v 和 Sl/Sl^d 小鼠。它们对于分析肥大细胞在体内生物反应中的作用的价值。”
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KITAMURA Yukihiko其他文献

KITAMURA Yukihiko的其他文献

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{{ truncateString('KITAMURA Yukihiko', 18)}}的其他基金

Regulation of Mast Cell Differentiation by mi Transcription Factor (MITE)
mi 转录因子 (MITE) 对肥大细胞分化的调节
  • 批准号:
    12002010
  • 财政年份:
    2000
  • 资助金额:
    $ 8.64万
  • 项目类别:
    Grant-in-Aid for Specially Promoted Research
Analysis of Phenotypic Variation of Mast Cells by Using Messenger RNA Expression as a Marker
以信使 RNA 表达为标志物分析肥大细胞表型变异
  • 批准号:
    06454193
  • 财政年份:
    1994
  • 资助金额:
    $ 8.64万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (B)
Regulation of Hemopoietic Stem Cells and Its Clinical Application
造血干细胞的调控及其临床应用
  • 批准号:
    06277103
  • 财政年份:
    1994
  • 资助金额:
    $ 8.64万
  • 项目类别:
    Grant-in-Aid for Scientific Research on Priority Areas
Development of Mutant Rats Useful for Analysis of Immediate Hypersensitivity
可用于速发型超敏反应分析的突变大鼠的培育
  • 批准号:
    03558010
  • 财政年份:
    1991
  • 资助金额:
    $ 8.64万
  • 项目类别:
    Grant-in-Aid for Developmental Scientific Research (B)
Fibroblast-dependent Proliferation of Mast Cells
肥大细胞成纤维细胞依赖性增殖
  • 批准号:
    02404030
  • 财政年份:
    1990
  • 资助金额:
    $ 8.64万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (A)

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使用 H19-ICR 突变小鼠组研究过度生长和异常高甲基化的分子机制
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ASD 突变小鼠模型的基因恢复和功能拯救
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    457197
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    10400428
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Establishment and Characterization of Novel Mutant Mouse Models for the Addiction Research Community
成瘾研究界新型突变小鼠模型的建立和表征
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运动轴突缺陷突变小鼠的遗传分析
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双侧投射突变小鼠皮质脊髓束功能的研究
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开发一个新平台,用于鉴定 Kras 和 Keap1 突变小鼠肺腺癌模型中的合成致死基因。
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确定 Mecp2 突变小鼠 Rett 综合征模型中肺脂质缺陷的机制
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