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Effects of cdc2 gene and EMC tenasc in on regulation of growth and differentiation of hematopoietic cells

Effects of cdc2 gene and EMC tenasc in on regulation of growth and differentiation of hematopoietic cells
cdc2基因和EMC tenasc对造血细胞生长和分化的调控作用
批准号:
04454575
负责人:
SAITO Masaki
金额:
$4.35万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for General Scientific Research (B)
财政年份:
1992
资助国家:
日本
项目状态:
已结题
起止时间:
1992 至 1993

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中文摘要
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英文摘要
Our recent research works brought about the following results : (1) Cdc2 mRNA transcript wasreadily detected in immature bone marrow cells and became undetectable accompanying with the cell cycle arrest which ocurred along wich differentiation : it was undetectable after the myelocyte/metamyelocyte stages in granulocytic differentiation. Peripheral blood resting cells including granulocytes, monocytes and T-lymphocytes did not express cdc2 mRNA transcripts. Cdc2 mRNA could be induced in T-lymphocytes when the cells re-entered the cell cycle in response to specific mitogens such as PHA.In contrast, cdc2 mRNA could not be induced in granulocytes and monocytes even after the culture with the appropriate stimulants such as LPS or CSFs. The changes in the chromatin structure such as the appearance of DNase I hypersensitivity sites or the slteration of DNA methylation status were not observed in T-lymphocytes even after the induction of cdc2 mRNA expression by mitogenic stimuli. Then, we isolated the regulatory sequence of cdc2 gene by a ligation-mediated PCR and found E2F binding site at the position of nt -117 to -124 and the RB control elements at the positions of nt -106 to -112 and -156 to -165. (2) Tenascin is a novel six-armed extracellular-matrix glycoprotein expressed in association with mesenchymal-epithelial interactions, and its expression is temporally restricted during oganogenesis and carcinogenesis. Immuoprecipitation studies revealed two ascites-hepatoma-derived cell lines and one sarcoma-derived line synthesized tenascin in vitro. The other cell lines examined, including all of those derived from normal hepatocytes, were negative for the expression of tenascin. Coculture studies were performed between epithelial and nonepithelial cell lines. No drastic change in tenascin expression was found after cocultuing the cells. As an in vivo study, cell lines were transplanted into nude mice. All xenografts of the epithelial lines were associated with a storong
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明石 真言、斎藤 政樹: "Annual Review 血液 1992(高久、青木、仁保、長尾編)[前骨髄球性白血病の分化誘導療法]" 中外医学社、東京, 8/259 (1992)
Shingon Akashi、Masaki Saito:“Annual Review Blood 1992(由 Takahisa、Aoki、Niho、Nagao 编辑)[早幼粒细胞白血病的分化诱导疗法]”Chugai Igakusha,东京,8/259 (1992)
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Sakai,T.,Kawakatsu,H.,Hirota,N.,et al.: "Specific Expression of Tenascin in Human Colonic Neoplasms." Br.J.Cancer. 67. 1058-1064 (1993)
Sakai,T.,Kawakatsu,H.,Hirota,N.,et al.:“腱蛋白在人结肠肿瘤中的特异性表达。”
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Ohsaka,A.,Kitagawa,S.,Yuo,A.,et al.: "Effects of granulocytes colony-stimulating factor and granulocyte-macrophage colony-stimulating factor on respiratory burst activity of neutrophils in patiecnts with myelodysplastic syndromes" Clin.Exp.lmmunol.91. 308
Ohsaka,A.,Kitakawa,S.,Yuo,A.,等人:“粒细胞集落刺激因子和粒细胞巨噬细胞集落刺激因子对骨髓增生异常综合征患者中性粒细胞呼吸爆发活性的影响”Clin.Exp
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27
    Molecular mechanisms of primary ciliary resorption and cilia-dependent cell cycle regulation.
    Functions of Complex Glycosphingolipids in the Cell Proliferation, Differentiation, and Cell Death Controlled at the Gene Level of Their Synthesizing Enzymes, and Their Medical Applications
    • 批准号:
      14370310
    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
      $9.02万
    • 财政年份:
      2002
    • 负责人:
      SAITO Masaki
    • 依托单位:
    Study on Ultra-Long Life Ores Lolled with Transuranium Fuels
    • 批准号:
      11694138
    • 项目类别:
      Grant-in-Aid for Scientific Research (A)
    • 资助金额:
      $10.52万
    • 财政年份:
      1999
    • 负责人:
      SAITO Masaki
    • 依托单位:
    Expression Mechanism and Its Medical Application of Ganglioside GM3 Synthase Gene Which Is Relevantly Related With Growth and Differentiation of Hematopoietic Cells
    • 批准号:
      10470206
    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
      $8.06万
    • 财政年份:
      1998
    • 负责人:
      SAITO Masaki
    • 依托单位: