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人干扰素诱导独特的信使核糖核酸

Induction of unique mRNAs by human interferons.

作者信息

Colonno R J, Pang R H

出版信息

J Biol Chem. 1982 Aug 25;257(16):9234-7.

PMID:6179932
Abstract

Treatment of human fibroblast cells with human interferon (INF-alpha, IFN-beta, or IFN-gamma) resulted in the accumulation of at least four newly synthesized mRNAs. The mRNAs code for proteins having molecular weights of 56,000, 57,000, 62,000, and 68,000 when characterized in a wheat germ cell-free translation system. A direct relationship was observed between the amount of IFN used and the degree of both the accumulation of the induced mRNAs and the development of an antiviral state. In the case of IFN-alpha or IFN-beta, time course studies indicated that the induced mRNAs appeared as early as 40 min, accumulated for 2 h, then remained ribosome bound for up to 16 h. The ability of fibroblast cells to develop an antiviral state always coincided directly with both the appearance and the level of accumulation of the induced mRNAs. Further mRNA synthesis beyond 2 h had a minimal effect on the development of an antiviral state. Human IFN-gamma also induced the synthesis of the same four mRNAs but required higher interferon titers and a longer incubation time. In addition, IFN-gamma induced a disproportionate amount of the mRNA coding for the 68,000 molecular weight protein and three new mRNAs not detected in cells treated with IFN-alpha or IFN-beta. Mouse interferon induces the original four mRNAs in human cells but to a far lesser extent. This correlated with the inability of these cells to develop much resistance to viral infection.

摘要

用人干扰素(α干扰素、β干扰素或γ干扰素)处理人成纤维细胞,导致至少四种新合成的mRNA积累。当在麦胚无细胞翻译系统中进行鉴定时,这些mRNA编码分子量分别为56,000、57,000、62,000和68,000的蛋白质。观察到所用干扰素的量与诱导的mRNA积累程度和抗病毒状态的发展程度之间存在直接关系。就α干扰素或β干扰素而言,时间进程研究表明,诱导的mRNA最早在40分钟出现,积累2小时,然后与核糖体结合长达16小时。成纤维细胞产生抗病毒状态的能力总是与诱导的mRNA的出现和积累水平直接相关。2小时后进一步的mRNA合成对抗病毒状态的发展影响最小。人γ干扰素也诱导相同的四种mRNA的合成,但需要更高的干扰素滴度和更长的孵育时间。此外,γ干扰素诱导编码68,000分子量蛋白质的mRNA以及在用α干扰素或β干扰素处理的细胞中未检测到的三种新mRNA的量不成比例。小鼠干扰素在人细胞中诱导原来的四种mRNA,但程度要小得多。这与这些细胞对病毒感染产生抗性的能力较弱相关。

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