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Isolation of Daudi cells with reduced sensitivity to interferon. I. Characterization.

作者信息

Dron M, Tovey M G

出版信息

J Gen Virol. 1983 Dec;64 ( Pt 12):2641-7. doi: 10.1099/0022-1317-64-12-2641.

DOI:10.1099/0022-1317-64-12-2641
PMID:6420510
Abstract

Treatment of Daudi cells with successively increasing concentrations of interferon-alpha resulted in the selection of a cell population which multiplied in the continued presence of 10(4) units/ml of interferon-alpha. A number of clones of interferon-resistant Daudi cells were isolated from this population. Two clones, DIF2 and DIF3, were found to exhibit moderate and pronounced resistance, respectively, to both the antiviral and antiproliferative actions of human interferons-alpha and -beta. These clones were also less responsive to the enhancement by interferon of Epstein-Barr virus early antigen expression. Both the surface antigens and karyotype of the interferon-resistant clones were similar to those of parental Daudi cells. After prolonged cultivation in the absence of interferon, DIF3 cells were found to 'revert' to an intermediate interferon sensitivity. The interferon sensitivity of clone DIF2 remained unchanged even after more than 1 year in culture.

摘要

相似文献

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引用本文的文献

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Mol Cell Biol. 1999 Nov;19(11):7305-13. doi: 10.1128/MCB.19.11.7305.
2
Increased rate of degradation of c-myc mRNA in interferon-treated Daudi cells.干扰素处理的Daudi细胞中c-myc信使核糖核酸降解速率增加。
Proc Natl Acad Sci U S A. 1985 Aug;82(15):4896-9. doi: 10.1073/pnas.82.15.4896.
3
Interferon modulation of c-myc expression in cloned Daudi cells: relationship to the phenotype of interferon resistance.
克隆的Daudi细胞中干扰素对c-myc表达的调节:与干扰素抗性表型的关系。
Mol Cell Biol. 1986 May;6(5):1374-8. doi: 10.1128/mcb.6.5.1374-1378.1986.
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Cells resistant to interferon are defective in activation of a promoter-binding factor.对干扰素耐药的细胞在启动子结合因子的激活方面存在缺陷。
EMBO J. 1988 Dec 1;7(12):3779-83. doi: 10.1002/j.1460-2075.1988.tb03262.x.
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Regulation of cell proliferation and differentiation by interferons.干扰素对细胞增殖和分化的调控。
Biochem J. 1985 Mar 1;226(2):345-60. doi: 10.1042/bj2260345.
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