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转染EB病毒DNA后人T淋巴细胞的永生化

Immortalization of human T lymphocytes after transfection of Epstein-Barr virus DNA.

作者信息

Stevenson M, Volsky B, Hedenskog M, Volsky D J

出版信息

Science. 1986 Aug 29;233(4767):980-4. doi: 10.1126/science.3016899.

DOI:10.1126/science.3016899
PMID:3016899
Abstract

Epstein-Barr virus (EBV), a ubiquitous human herpesvirus, has the ability to transform human B lymphocytes. No other cell type has been experimentally transformed by EBV, either by intact virions or naked viral DNA and subgenomic fragments. Two immortalized human T-lymphoblastoid cell lines have now been established by transfecting cord blood lymphocytes with purified B95-8 viral DNA enclosed in fusogenic Sendai virus envelopes (RSVE) and then exposing the cells to EBV from a P3HR-1 cell subclone. One of these lines, which has been fully characterized, is termed HBD-1. This line is positive for EBV DNA and expresses surface OKT11, OKT4, and Tac receptors, but not M-1, mu immunoglobulin chains, EBV receptors, or B-1 surface markers. The cells contain fully rearranged T-cell receptor genes and germline immunoglobulin genes. The karyotype of the cells is normal, they do not require interleukin-2 for growth, and do not contain human T-lymphotropic virus type I. However, the HBD-1 cells contain incomplete EBV genomes and express several EBV-determined antigens, including the early antigen type D, membrane antigens, but not EBV-determined nuclear antigen (EBNA). This association of the EBV genome with permanently growing hematopoietic cells of non B-cell lineage should prove useful in studies on the mechanism of EBV-mediated cell transformation.

摘要

爱泼斯坦-巴尔病毒(EBV)是一种普遍存在的人类疱疹病毒,具有转化人类B淋巴细胞的能力。无论是完整的病毒体还是裸露的病毒DNA及亚基因组片段,都未通过实验使其他细胞类型被EBV转化。现在,通过用包裹在融合性仙台病毒包膜(RSVE)中的纯化B95-8病毒DNA转染脐血淋巴细胞,然后将这些细胞暴露于来自P3HR-1细胞亚克隆的EBV,已建立了两个永生化的人类T淋巴母细胞系。其中一个已被充分鉴定的系被称为HBD-1。该系EBV DNA呈阳性,表达表面OKT11、OKT4和Tac受体,但不表达M-1、μ免疫球蛋白链、EBV受体或B-1表面标志物。这些细胞含有完全重排的T细胞受体基因和种系免疫球蛋白基因。细胞的核型正常,生长不需要白细胞介素-2,也不含有I型人类嗜T淋巴细胞病毒。然而,HBD-1细胞含有不完整的EBV基因组,表达几种EBV决定的抗原,包括D型早期抗原、膜抗原,但不表达EBV决定的核抗原(EBNA)。EBV基因组与非B细胞系的永久生长造血细胞的这种关联在研究EBV介导的细胞转化机制中应会证明是有用的。

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Immortalization of human T lymphocytes after transfection of Epstein-Barr virus DNA.转染EB病毒DNA后人T淋巴细胞的永生化
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2
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EBNA-2 -deleted Epstein-Barr virus from P3HR-1 can infect rabbits with lower efficiency than prototype Epstein-Barr virus from B95-8.P3HR-1 缺失 EBNA-2 的 EBV 比 B95-8 原型 EBV 感染兔子的效率低。
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Rescue of transforming Epstein-Barr virus (EBV) from EBV-genome-positive epithelial hybrid cells transfected with subgenomic fragments of EBV DNA.从用爱泼斯坦-巴尔病毒(EBV)DNA亚基因组片段转染的EBV基因组阳性上皮杂交细胞中拯救转化型EBV。
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引用本文的文献

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Improvement of a method to reproducibly immortalize human T cells by oncogene transfection.通过癌基因转染可重复性地永生化人 T 细胞的方法的改进。
Cytotechnology. 2000 Jul;33(1-3):71-81. doi: 10.1023/A:1008171109981.
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Immortalization of human T lymphocytes by oncogenes.癌基因对人T淋巴细胞的永生化作用。
Cytotechnology. 1993;11(3):205-11. doi: 10.1007/BF00749871.
4
Downregulation of cell surface molecules during noncytopathic infection of T cells with human immunodeficiency virus.人免疫缺陷病毒对T细胞进行非细胞病变感染期间细胞表面分子的下调
J Virol. 1987 Dec;61(12):3741-8. doi: 10.1128/JVI.61.12.3741-3748.1987.
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Characterization of a T-lymphocyte Epstein-Barr virus/C3d receptor (CD21).
J Virol. 1988 Apr;62(4):1442-7. doi: 10.1128/JVI.62.4.1442-1447.1988.
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Influence of Burkitt's lymphoma and primary B cells on latent gene expression by the nonimmortalizing P3J-HR-1 strain of Epstein-Barr virus.伯基特淋巴瘤和原代B细胞对爱泼斯坦-巴尔病毒非永生化P3J-HR-1株潜伏基因表达的影响。
J Virol. 1989 Apr;63(4):1531-9. doi: 10.1128/JVI.63.4.1531-1539.1989.
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Use of an Epstein-Barr virus episomal replicon for anti-sense RNA-mediated gene inhibition in a human cytotoxic T-cell clone.使用爱泼斯坦-巴尔病毒附加型复制子在人细胞毒性T细胞克隆中进行反义RNA介导的基因抑制。
Proc Natl Acad Sci U S A. 1988 Jun;85(11):4010-4. doi: 10.1073/pnas.85.11.4010.
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Common variable immunodeficiency and malignancy: a report of two cases and possible explanation for the association.普通可变免疫缺陷与恶性肿瘤:两例报告及关联的可能解释
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Induction and progression of human lymphoproliferative lesions by Epstein-Barr virus.爱泼斯坦-巴尔病毒引发及促进人类淋巴增殖性病变
Environ Health Perspect. 1990 Aug;88:237-41. doi: 10.1289/ehp.9088237.
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