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对一种源自霍奇金病的新型细胞系进行细胞化学、免疫学、染色体及分子遗传学分析。

Cytochemical, immunologic, chromosomal, and molecular genetic analysis of a novel cell line derived from Hodgkin's disease.

作者信息

Kamesaki H, Fukuhara S, Tatsumi E, Uchino H, Yamabe H, Miwa H, Shirakawa S, Hatanaka M, Honjo T

出版信息

Blood. 1986 Jul;68(1):285-92.

PMID:3013343
Abstract

A novel cell line, KM-H2, was established from the pleural effusion of a patient with Hodgkin's disease of mixed cellular type. Multiple phenotypic studies were carried out with this cell line. Acid phosphatase and nonspecific esterase activities were detected. Rosette formation with T lymphocytes and the receptors for C3b and Fc portion of IgG were positive. Among the antigens tested with a total of 22 monoclonal antibodies defining hematopoietic cell subsets or lineages, Ki-1, Leu-M1, MCS1, HLA-DR, and OKT9 antigens were found to be positive. The other antigens reportedly specific for T cells, B cells, natural killer (NK) cells, monocytes, interdigitating reticulum (IR) cells and dendritic reticulum cells were negative. These phenotypic features were identical to those of the Sternberg-Reed (SR) and Hodgkin (H) cells in the fresh materials reported by other researchers. Moreover, the KM-H2 cells and the parental pleural effusion cells shared several structural chromosome anomalies. These findings indicated that the KM-H2 cells are derived from the SR and H cells. Molecular genetic analysis of the KM-H2 cells disclosed that the human immunoglobulin JH gene was rearranged but not the JK gene, and that the human T cell receptor beta chain gene was of the germline type. Based on these properties of the KM-H2 cells, Hodgkin's disease may be derived from a cell lineage other than T cell or B cell.

摘要

一种新的细胞系KM-H2是从一名混合细胞型霍奇金病患者的胸腔积液中建立的。对该细胞系进行了多项表型研究。检测到酸性磷酸酶和非特异性酯酶活性。与T淋巴细胞形成玫瑰花结以及对IgG的C3b和Fc部分的受体呈阳性。在用总共22种定义造血细胞亚群或谱系的单克隆抗体检测的抗原中,发现Ki-1、Leu-M1、MCS1、HLA-DR和OKT9抗原呈阳性。据报道,其他对T细胞、B细胞、自然杀伤(NK)细胞、单核细胞、交错突网状(IR)细胞和树突状网状细胞特异的抗原为阴性。这些表型特征与其他研究人员报道的新鲜材料中的施特恩伯格-里德(SR)细胞和霍奇金(H)细胞的表型特征相同。此外,KM-H2细胞和亲本胸腔积液细胞共有几个结构染色体异常。这些发现表明,KM-H2细胞来源于SR细胞和H细胞。对KM-H2细胞的分子遗传学分析表明,人免疫球蛋白JH基因发生了重排,但JK基因未重排,并且人T细胞受体β链基因属于种系类型。基于KM-H2细胞的这些特性,霍奇金病可能来源于T细胞或B细胞以外的细胞谱系。

相似文献

1
Cytochemical, immunologic, chromosomal, and molecular genetic analysis of a novel cell line derived from Hodgkin's disease.对一种源自霍奇金病的新型细胞系进行细胞化学、免疫学、染色体及分子遗传学分析。
Blood. 1986 Jul;68(1):285-92.
2
SUP-HD1: a new Hodgkin's disease-derived cell line with lymphoid features produces interferon-gamma.SUP-HD1:一种具有淋巴细胞特征的新型霍奇金淋巴瘤衍生细胞系可产生γ干扰素。
Blood. 1989 Dec;74(8):2733-42.
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Phenotypic expression of Hodgkin's and Reed-Sternberg cells in Hodgkin's disease.霍奇金病中霍奇金和里德-斯腾伯格细胞的表型表达。
Am J Pathol. 1985 Feb;118(2):209-17.
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Morphologic, immunologic, enzymehistochemical and chromosomal analysis of a cell line derived from Hodgkin's disease. Evidence for a B-cell origin of Sternberg-Reed cells.对源自霍奇金病的细胞系进行形态学、免疫学、酶组织化学和染色体分析。支持斯腾伯格-里德细胞起源于B细胞的证据。
Cancer. 1985 Feb 15;55(4):683-90. doi: 10.1002/1097-0142(19850215)55:4<683::aid-cncr2820550402>3.0.co;2-o.
5
Hodgkin's disease: establishment and characterization of four in vitro cell lies.霍奇金病:四种体外细胞系的建立与鉴定
J Cancer Res Clin Oncol. 1981;101(1):111-24. doi: 10.1007/BF00405072.
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Monoclonal antibodies in the diagnosis of Hodgkin's disease. The search for a rational panel.单克隆抗体在霍奇金病诊断中的应用。寻找合理的检测组合。
Am J Surg Pathol. 1988 Jan;12(1):9-21. doi: 10.1097/00000478-198801000-00002.
7
Immunopathology of Hodgkin's disease. Characterization of Reed-Sternberg cells with monoclonal antibodies.霍奇金病的免疫病理学。用单克隆抗体对里德-斯腾伯格细胞进行特征描述。
Am J Pathol. 1986 May;123(2):293-300.
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Identification of Hodgkin and Sternberg-reed cells as a unique cell type derived from a newly-detected small-cell population.将霍奇金细胞和施特恩伯格-里德细胞鉴定为源自新检测到的小细胞群体的独特细胞类型。
Int J Cancer. 1982 Oct 15;30(4):445-59. doi: 10.1002/ijc.2910300411.
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Two neoplastic cell lines with unique features derived from Hodgkin's disease.两种具有独特特征的肿瘤细胞系,源自霍奇金淋巴瘤。
Int J Cancer. 1980 Dec 15;26(6):723-31. doi: 10.1002/ijc.2910260605.
10
Genotypes and immunophenotypes of Hodgkin's disease-derived cell lines.霍奇金病来源细胞系的基因型和免疫表型
Leukemia. 1988 Jun;2(6):371-6.

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