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一种新的髓系白血病细胞系(TK-1)的建立以及涉及17q23带易位的细胞的分离。

Establishment of a new myeloid leukemia cell line (TK-1), and isolation of cells having a translocation involving a band 17q23.

作者信息

Ohno H, Doi S, Fukuhara S, Yamasowa M, Kannagi M, Ishikura H, Nishikori M, Uchino H

出版信息

Int J Cancer. 1986 May 15;37(5):761-7. doi: 10.1002/ijc.2910370518.

DOI:10.1002/ijc.2910370518
PMID:3457771
Abstract

A myeloid leukemia cell line (TK-1) was established from the peripheral blood of a patient with lymphoblastic lymphoma whose leukemia cells were composed of T-lymphoblasts and immature myeloid cells. The established TK-1 cell line consisted of immature myeloid cells with heavy azurophilic granulation in the cytoplasm. The TK-1 cells were positive for peroxidase, and exhibited a strong positive reaction for alpha-naphthyl acetate esterase and naphthol AS-D chloroacetate esterase. The cells were weakly positive for Fc gamma-receptors, showed no phagocytosis and did not reduce NBT. With the treatment of 1 alpha, 25-dihydroxy-vitamin D3, they exhibited morphological and functional differentiation. The TK-1 cell line contained normal diploid cells and pseudodiploid cells, and the two populations were successfully cloned; the clone with a normal karyotype was designated the TK-1D cell line, and the clone with a pseudodiploid karyotype, which had a translocation involving chromosomes 14, 17 and one other chromosome, was designated the TK-1B cell line. These cloned cells lacked Epstein-Barr virus nuclear antigens and had almost the same myelomonocytic characteristics as the parent TK-1 cells. The breakpoint of chromosome 17 involved in the translocation of the pseudodiploid cells was identified to be a band 17q23.

摘要

一种髓系白血病细胞系(TK - 1)是从一名淋巴细胞淋巴瘤患者的外周血中建立的,该患者的白血病细胞由T淋巴细胞和未成熟髓细胞组成。所建立的TK - 1细胞系由细胞质中具有粗大嗜天青颗粒的未成熟髓细胞组成。TK - 1细胞过氧化物酶呈阳性,对α - 萘乙酸酯酶和萘酚AS - D氯乙酸酯酶呈强阳性反应。细胞对Fcγ受体呈弱阳性,无吞噬作用,不还原NBT。用1α,25 - 二羟基维生素D3处理后,它们表现出形态和功能分化。TK - 1细胞系包含正常二倍体细胞和假二倍体细胞,并且这两个群体成功克隆;具有正常核型的克隆被命名为TK - 1D细胞系,具有假二倍体核型且涉及14号、17号染色体和另一条染色体易位的克隆被命名为TK - 1B细胞系。这些克隆细胞缺乏EB病毒核抗原,并且具有与亲本TK - 1细胞几乎相同的髓单核细胞特征。假二倍体细胞易位中涉及的17号染色体的断点被确定为17q23带。

相似文献

1
Establishment of a new myeloid leukemia cell line (TK-1), and isolation of cells having a translocation involving a band 17q23.一种新的髓系白血病细胞系(TK-1)的建立以及涉及17q23带易位的细胞的分离。
Int J Cancer. 1986 May 15;37(5):761-7. doi: 10.1002/ijc.2910370518.
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Establishment of a new peroxidase-positive human myeloid cell line, PL-21.一种新的过氧化物酶阳性人髓系细胞系PL-21的建立。
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Establishment of a novel acute monoblastic leukemia cell line (YK-M2) having a near-triploid karyotype.建立一种具有近三倍体核型的新型急性单核细胞白血病细胞系(YK-M2)。
Cancer Res. 1986 Dec;46(12 Pt 1):6400-5.
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Characterization of a new chromosomal marker for acute lymphoblastic leukemia from a long-term cell line.来自长期细胞系的急性淋巴细胞白血病新染色体标志物的特征分析。
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Phenotypic conversion of T lymphoblastic lymphoma to acute biphenotypic leukemia composed of lymphoblasts and myeloblasts. Molecular genetic evidence of the same clonal origin.T淋巴母细胞淋巴瘤向由淋巴母细胞和髓母细胞组成的急性双表型白血病的表型转化。同一克隆起源的分子遗传学证据。
J Clin Invest. 1988 Jun;81(6):1824-8. doi: 10.1172/JCI113526.
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Chromosome abnormalities in leukemia and lymphoma.白血病和淋巴瘤中的染色体异常。
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Establishment of a Ph1 chromosome-positive cell line from chronic myelogenous leukemia in blast crisis.从处于急变期的慢性髓性白血病中建立Ph1染色体阳性细胞系。
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RCH-ACV: a lymphoblastic leukemia cell line with chromosome translocation 1;19 and trisomy 8.RCH-ACV:一种具有1;19染色体易位和8号染色体三体的淋巴细胞白血病细胞系。
Cancer Genet Cytogenet. 1986 Jan 15;19(3-4):261-9. doi: 10.1016/0165-4608(86)90055-5.
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Establishment and characterization of a common acute lymphoblastic leukemia cell line with a deletion of chromosome 3 band q26.一种3号染色体q26带缺失的常见急性淋巴细胞白血病细胞系的建立与鉴定
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t(11;19)(q23;p11) in a child with acute T-cell leukemia.一名急性T细胞白血病患儿存在t(11;19)(q23;p11)。
Cancer Genet Cytogenet. 1985 Feb 1;15(1-2):181-5. doi: 10.1016/0165-4608(85)90147-5.

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Phenotypic conversion of T lymphoblastic lymphoma to acute biphenotypic leukemia composed of lymphoblasts and myeloblasts. Molecular genetic evidence of the same clonal origin.T淋巴母细胞淋巴瘤向由淋巴母细胞和髓母细胞组成的急性双表型白血病的表型转化。同一克隆起源的分子遗传学证据。
J Clin Invest. 1988 Jun;81(6):1824-8. doi: 10.1172/JCI113526.