Regulation of interferon action in human fibroblasts: transient induction of specific proteins and amplification of the antiviral response by antinomycin D.
Regulation of interferon action in human fibroblasts: transient induction of specific proteins and amplification of the antiviral response by antinomycin D.
复制标题
人成纤维细胞中干扰素作用的调节:特定蛋白质的瞬时诱导和抗霉素 D 抗病毒反应的放大。
DOI:
10.1016/0042-6822(81)90337-8
复制
发表时间:
1981
期刊:
影响因子:
3.7
通讯作者:
Holmes,SL
中科院分区:
文献类型:
--
作者:
Gupta,SL;Rubin,BY;Holmes,SL
We reported earlier that interferon treatment of human fibroblasts induces a number of proteins, and that this induction seems to correlate with the development of the antiviral state. The accumulation of interferon-induced proteins reaches a maximum within a few hr after interferon treatment and is then followed by a marked decline despite the continued presence of interferon in the medium indicating that this induction may be subject to regulation. Inhibitors of RNA synthesis (actinomycin D, 5,6-dichloro-1-β-d-ribofuranosylbenzimidazole) were found to have a dual effect on the antiviral action of interferon. When added together with interferon, they blocked the development of the antiviral state. In contrast, when added at later intervals (4–8 hr after interferon), the antiviral effect was greatly amplified. This amplification was associated with increased levels of various interferon-induced proteins and 2′,5′-oligoadenylate synthetase enzyme activity. The results indicate that the cellular response to interferon is subject to regulation and can be manipulated. Evidence is also presented which indicates that the interferon-induced genetic transcription required for the development of the antiviral state may extend for several hours.