STUDIES ON ORIGIN AND PROPERTIES OF A HODGIN CELL LINE, HPL-Hod-2, WHICH PRODUCE CYTOPLASMIC IgG
STUDIES ON ORIGIN AND PROPERTIES OF A HODGIN CELL LINE, HPL-Hod-2, WHICH PRODUCE CYTOPLASMIC IgG
批准号:
10670159
负责人:
MORIKAWA Shigeru
金额:
$1.98万
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
1998
资助国家:
日本
项目状态:
已结题
起止时间:
1998 至 1999
中文摘要
霍奇金病是一种独特的恶性淋巴瘤,其特征在于Reed-Sternberg(R-S)细胞和霍奇金(H)细胞的增殖,其正常对应物尚未被鉴定,虽然最近的证据表明是淋巴起源的。本项目旨在阐明R-S和H细胞的正常对应物,并进一步分析其生物学特性,以了解霍奇金病的发病机制。超过21个长期-从恶性淋巴瘤和白血病患者的胸腔积液中建立了HPL-Hod-2(Hod-2)细胞系,Hod-2细胞具有R-S和H细胞共同的细胞标志物,如CD 15,CD 25,Hod-2细胞表面表达CD 83,但其表面免疫球蛋白(IgG)的表达与Hod-2细胞表面表达的IgG分子大小基本相同,但其表面IgG分子大小与Hod-2细胞表面的IgG分子大小基本相同,而Hod-2细胞表面的IgG分子大小与Hod-2细胞表面的IgG分子大小基本相同。CD 83被认为是树突状细胞最可靠的标志物,在21株人恶性淋巴瘤/白血病细胞系中,除Hod-2细胞外,一株毛状白血病细胞系和一株B细胞恶性淋巴瘤细胞系的细胞浆中均弱表达CD 83。
英文摘要
Hodgkin's disease is a unique malignant lymphoma characterized by proliferation of Reed-Sternberg (R-S) cells and Hodgkin (H) cells, whose normal counterpart have not yet been identified, although the most recent evidence suggests a lymphoid origin.This project aim to elucidate normal counterpart of R-S and H cells and further to analysis their biological properties to understand pathogenesis of Hodgkin's disease.More than 21 long-term cultured cell lines derived from patients with malignant lymphoma and leukemia were investigated their immunological properties> Among them, HPL-Hod-2 (Hod-2), a lymphoblastoid cell line had been established from pleural effusion of a patient with Hodgkin's disease> Hod-2 cells shared common cell markers of R-S and H cells such as, CD15, CD25, CD30 and possessed pretty amount of IgG in their cytoplasms.But, they lacked surface immunoglobulin expression.Molecular analysis revealed these IgG consisted of H-chains and k-chains with almost equal molecular size to cytoplasmic IgG of ordinary B-cells.Interestingly enough, it was found that Hod-2 cells express CD83 on their cell surface. CD83 is thought to be the most reliable makers of dendritic cells.Among 21 human malignant lymphoma / leukemia cell lines, one hairly leukemia cell one and one B-cell malignant lymphoma cell line express weakly CD83 in their cytoplasms besides Hod-2 cells.In conclusion ; this investigation revealed the presence of B-lineage DC and their possible original cells of H and R-S cells.
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Nagasaki, M., Morikawa, S., Torii, I., Zhang, J., and Morikawa, K.: "A human B-lineage dendritic cell line, HBM-Noda and its potential role in GTLV-I infection"Pathol. Int.. 50 (in press). (2000)
Nagasaki, M.、Morikawa, S.、Torii, I.、Zhang, J. 和 Morikawa, K.:“人类 B 系树突状细胞系 HBM-Noda 及其在 GTLV-I 感染中的潜在作用”Pathol
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Nagasaki, M.: "A human B-lineage dendritic cell line, HBM-Noda and its potential role in HTLV-1 infection"Pathology International. (in press). (2000)
Nagasaki, M.:“人类 B 谱系树突状细胞系 HBM-Noda 及其在 HTLV-1 感染中的潜在作用”国际病理学。
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Nagasaki, M.: "Leukocyte typing VI (ed. by Kishimoto, T., et al.)"Garland Publishing, Inc. N.Y.. 592-593 (1998)
Nagasaki, M.:“白细胞分型 VI(由 Kishimoto, T. 等编辑)”Garland Publishing, Inc. N.Y. 592-593 (1998)
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Morikawa,K.: "Deoxyspergualin preferentially inhibits the growth and maturation of anti-CD40-activated surface IgD^+B lymphocytes."Clin.Exp.Immunol. 112・2. 495-500 (1998)
Morikawa, K.:“脱氧精胍菌素优先抑制抗 CD40 激活的表面 IgD^+B 淋巴细胞的生长和成熟。”Clin.Exp.Immunol. 112・2(1998)。
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Nagasaki,M.: "Leukocyte typing VI(ed. by Kishimoto,T.,etal.)"Garland Publishing,Inc.N.Y.. 2 (1998)
Nagasaki,M.:“白细胞分型 VI(岸本 T. 等编辑)”Garland Publishing, Inc.N.Y.. 2 (1998)
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共 8 条
Risk analysis of emerging zoonotic viral diseases caused by recently identified bunyaviruses and rhabdoviruses
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批准号:25450438
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$3.33万
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财政年份:2013
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负责人:MORIKAWA Shigeru
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依托单位:
Mast Cell-dependent Delayed Hypersensitivity (Jones-Mote type) and Analysis for Cellular Mechanism of the Response.
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批准号:63570164
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项目类别:Grant-in-Aid for General Scientific Research (C)
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资助金额:$1.34万
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财政年份:1988
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负责人:MORIKAWA Shigeru
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依托单位:
海外基金