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RD - 114细胞系的克隆衍生物对干扰素的抗病毒和基因诱导反应有所不同。

Clonal derivatives of the RD-114 cell line differ in their antiviral and gene-inducing responses to interferons.

作者信息

Kumar R, Tiwari R K, Kusari J, Sen G C

出版信息

J Virol. 1987 Sep;61(9):2727-32. doi: 10.1128/JVI.61.9.2727-2732.1987.

Abstract

The human rhabdomyosarcoma cell line RD-114 is partially responsive to interferons (IFNs). In these cells, alpha interferon (IFN-alpha) or gamma interferon (IFN-gamma) inhibits the replication of some viruses but not of others. Similarly, some of the IFN-inducible mRNAs are induced poorly, whereas others are induced well. Here we report the isolation of clonal derivatives of this line which display different spectra of responses to IFNs. Among the eight extensively characterized clonal lines, one, C10, did not respond to IFN-alpha or IFN-gamma at all. Retrovirus production by each of the seven other lines was inhibited by both IFN-alpha and IFN-gamma. Replication of vesicular stomatitis virus was inhibited strongly by IFN-alpha in clone B1 but not in others, whereas it was not appreciably affected by IFN-gamma in any clone. Replication of encephalomyocarditis virus was inhibited strongly by IFN-gamma in clones A1, A2, A3, B3, and B8 and by IFN-alpha in clone A2. Neither IFN inhibited the multiplication of these clones greatly, although their doubling times were slightly increased. Five mRNAs were induced by IFNs to varying degrees in the seven clones. mRNA 2A was most strongly induced by IFN-gamma in clone A3. mRNA 1-8 was strongly induced by IFN-alpha in clone A1 and by either IFN in clones A2 and A3. The highest concentrations of 2',5'-oligoadenylate synthetase mRNA, mRNA 561, and mRNA 6-16 were in IFN-alpha-treated clones A1 and A2. These results demonstrated the existence of clonal heterogeneity in IFN responses in a cell line and strengthened the view that IFN treatment of cells generates multiple signals leading to a variety of IFN-induced phenotypes.

摘要

人横纹肌肉瘤细胞系RD - 114对干扰素(IFN)有部分反应。在这些细胞中,α干扰素(IFN -α)或γ干扰素(IFN -γ)可抑制某些病毒的复制,但对其他病毒则无此作用。同样,一些IFN诱导的mRNA诱导程度较差,而另一些则诱导良好。在此,我们报告了该细胞系克隆衍生物的分离,这些衍生物对IFN表现出不同的反应谱。在八个经过广泛表征的克隆系中,一个名为C10的克隆系对IFN -α或IFN -γ完全无反应。其他七个克隆系产生逆转录病毒均受到IFN -α和IFN -γ的抑制。水泡性口炎病毒的复制在克隆B1中受到IFN -α的强烈抑制,而在其他克隆中则未受抑制,而在任何克隆中,IFN -γ对其复制均无明显影响。脑心肌炎病毒的复制在克隆A1、A2、A3、B3和B8中受到IFN -γ的强烈抑制,在克隆A2中受到IFN -α的强烈抑制。尽管这些克隆的倍增时间略有增加,但两种IFN均未显著抑制它们的增殖。在这七个克隆中,有五种mRNA受到IFN不同程度的诱导。mRNA 2A在克隆A3中受到IFN -γ的诱导最强。mRNA 1 - 8在克隆A1中受到IFN -α的强烈诱导,在克隆A2和A3中受到两种IFN的强烈诱导。2',5'-寡腺苷酸合成酶mRNA、mRNA 561和mRNA 6 - 16的最高浓度出现在经IFN -α处理的克隆A1和A2中。这些结果证明了在一个细胞系中IFN反应存在克隆异质性,并强化了这样一种观点,即对细胞进行IFN处理会产生多种信号,导致多种IFN诱导的表型。

相似文献

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Expression of interferon-inducible genes in RD-114 cells.
J Virol. 1987 May;61(5):1524-31. doi: 10.1128/JVI.61.5.1524-1531.1987.

本文引用的文献

5
Biochemical pathways in interferon-action.
Pharmacol Ther. 1984;24(2):235-57. doi: 10.1016/0163-7258(84)90036-6.
8
Biochemistry of interferons and their actions.干扰素的生物化学及其作用
Annu Rev Biochem. 1982;51:251-82. doi: 10.1146/annurev.bi.51.070182.001343.
9
Transcriptional analyses of interferon-inducible mRNAs.干扰素诱导mRNA的转录分析。
Mol Cell Biol. 1987 Jan;7(1):528-31. doi: 10.1128/mcb.7.1.528-531.1987.
10
Expression of interferon-inducible genes in RD-114 cells.
J Virol. 1987 May;61(5):1524-31. doi: 10.1128/JVI.61.5.1524-1531.1987.

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