Study on a fraction with relative radioresistency from murine pluripotent hemopoietic stem cells.
Study on a fraction with relative radioresistency from murine pluripotent hemopoietic stem cells.
批准号:
02807042
负责人:
INOUE Tohru
金额:
$1.02万
依托单位国家:
日本
项目类别:
Grant-in-Aid for General Scientific Research (C)
财政年份:
1990
资助国家:
日本
项目状态:
已结题
起止时间:
1990 至 1991
中文摘要
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英文摘要
According to our suty on tridated thymidine cytocide, a colony forming unit in spleen (CFLJ-S) can. be divided into two major fractions ; i. e. stem cells possessing less pluripotency in differentiation with a Idnetics largely in S phase (the progenitor cells producing early appearing colonies), and the other ones possessing quiescent nature without cell cycle (the progenitor cells producing late appearing colonies). While former fraction reacts at larger extent to a variety of hemopoietic stimuli, latter does but relatively at a smaller extent. The heterogeneity of the CFU-S, as seen above, suggestes a heterogeneous radiation sensifivity in 6ach sub-fraction, however, none has been actually demonstrated pertaining to this heterogeneous radiation sensitivity. Bone marrow cells were irradiated with 400 cOy through 600 eGy, in vitro, and then been injected with lethally irradiated mice to form spleen colonies. There was a fraction found after these relatively larger dose of radiation at … More larger extent than numbers estimated by a survival curve fitting to a single-exponential model ; namely, the steep regular survival curve (D_0=90 cGy) changed into a flatter bne (D_0=270 cGy) after 300 through 400 cGy, probably because of a small radiosensitive subfraction, ca. 3-5%, mixed. with the regular CFLJ-S. This was confirmed by a variety of different murine stanns in our research project. Although irradiation was given at in vitro, oxygen effects must be minimum or none, and actually, no effects might have been involved in a mechanism of these flatter part of the survival curve, since total radiation time took for each fraction was ca. 4 min. and 14 sec. and or less. During these studies, we incidentally found another important finding in the Scid mice pertaining to the radioresistant fraction of the CFLJ-S. Originally, somatic cells in Scid mutaidon have been found to be very mioresistant because of a functional defect of repair for double strand breaks. We found, under the surveillance of D_0 in the Scid mice, again, a relatively radioresistant fraction sharply defined from the regular CFU-S. This phenomenon would deal with further study of this research program. Less
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Nishimura M,kaku K,Azuno Y,Okafuji K,Etoh Y,Shiozaki,H,Inoue T,Kaneko T.: "Effect of erythroid differentiation factor on megakaryocytic differentiation of L8057,a murine megakaryoblastic leukemia cell line." Biochem Biophys Res Comm. 181(3). 1942-1047 (19
Nishimura M,kaku K,Azuno Y,Okafuji K,Etoh Y,Shiozaki,H,Inoue T,Kaneko T.:“红系分化因子对小鼠巨核细胞白血病细胞系 L8057 巨核细胞分化的影响。”
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通讯作者:
Fujimoto K, Kawakita M, Kato K, Yonemura Y, Masuda T, Matsuzatki et al.: "Purification of megakaryocyte differentiation activity from a fibrous histiocytoma cell line : N-terminal sequence homology to Activin A." Boichem. riophys. Res. Comm.174. 1163-1168
Fujimoto K、Kawakita M、Kato K、Yonemura Y、Masuda T、Matsuzatki 等人:“从纤维组织细胞瘤细胞系中纯化巨核细胞分化活性:与激活素 A 的 N 端序列同源性。”
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Hirabayashi Y, and Inoue T.: "Hemopoietic microenvironment during ageing. (in Japanese)" Hematology & Oncology. 23(3). 193-201 (1991)
Hirabayashi Y 和 Inoue T.:“衰老过程中的造血微环境。(日语)”血液学
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Hirabayashi Y,Inoue T,Yoshida K,Sasaki H,Kubo S,Kanisawa M et al.: "Murine acute leukemia cell line with a single megakaryocytic differentiation(MK8057),induced by whole body irradiation in C3H.He mice: Cytological properties and kinetics of its leukemic
Hirabayashi Y、Inoue T、Yoshida K、Sasaki H、Kubo S、Kanisawa M 等人:“具有单一巨核细胞分化的小鼠急性白血病细胞系 (MK8057),通过 C3H 全身照射诱导。He 小鼠:细胞学特性和
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Hirabayashi Y,Inoue T,Yoshida K,Inayama Y,Kanisawa M.: "The detection of normal hidden stem cells during the development of leukemia:Assays with PGK isozyme." Exptl Hematol. 18. 289-296 (1990)
Hirabayashi Y、Inoue T、Yoshida K、Inayama Y、Kanisawa M.:“白血病发展过程中正常隐藏干细胞的检测:PGK 同工酶测定。”
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共 36 条
Toxicity mechanism in hematopoietic stem/progenitor-derived signaling via aryl hydrocarbon receptors induced by benzene exposure
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批准号:21510074
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$3.0万
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财政年份:2009
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负责人:INOUE Tohru
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依托单位:
Biological function of aryl hydrocarbon receptors in the hematopoietic progenitor cells with respect to a possible toxicologic mechanism
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批准号:18510066
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.75万
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财政年份:2006
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负责人:INOUE Tohru
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依托单位:
Mechanism of benzene-induced hematopoietic disturbances mediated by arylhydrocarbon receptors
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批准号:15510064
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$1.98万
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财政年份:2003
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负责人:INOUE Tohru
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依托单位:
Blocks of cell communication and apoptosis in carcinogenesis
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批准号:11694334
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项目类别:Grant-in-Aid for Scientific Research (B).
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资助金额:$1.66万
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财政年份:1999
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负责人:INOUE Tohru
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依托单位:
Study on the signal cross talk bencath the Arythydroearbon receptor in the hemopoietic stem cells.
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批准号:11670234
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.11万
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财政年份:1999
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负责人:INOUE Tohru
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依托单位:
p53 null mice and chemical oncogenesis for promotion study
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批准号:09044353
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项目类别:Grant-in-Aid for international Scientific Research
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资助金额:$2.05万
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财政年份:1997
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负责人:INOUE Tohru
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依托单位:
Signal transduction mediated by hematopoietic factors and TGF-β in p53-deficient mice
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批准号:08457079
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项目类别:Grant-in-Aid for Scientific Research (B)
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资助金额:$2.24万
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财政年份:1996
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负责人:INOUE Tohru
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依托单位:
Construction of mouse embryonic stem cells for the detection of gene mutation
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批准号:08559016
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项目类别:Grant-in-Aid for Scientific Research (A)
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资助金额:$4.61万
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财政年份:1996
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负责人:INOUE Tohru
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依托单位: