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用代谢抑制剂超诱导干扰素:可能的机制及实际应用

Superinduction of interferon with metabolic inhibitors: possible mechanisms and practical applications.

作者信息

Vilcek J, Havell E A, Kohase M

出版信息

J Infect Dis. 1976 Jun;133 Suppl:A22-9. doi: 10.1093/infdis/133.supplement_2.a22.

DOI:10.1093/infdis/133.supplement_2.a22
PMID:778308
Abstract

Ten years have passed since cycloheximide was first shown to enhance endotoxin-induced production of interferon in mice, in the first demonstration of what was later called the superinduction of interferon. Various inhibitors of protein and RNA symthesis, as well as combinations of these inhibitors, have been shown to act as superinducing agents of interferon production stimulated by polyriboinosinic-polyribocytidylic acid. The evidence that superinduction is due to the suppression of a mechanism of post-transcriptional regulation of interferon synthesis is rather convincing. The notion (first proposed about six years ago) that this modification is caused by a protein "repressor" remains the most plausible, albeit still unproved, hypothesis. The availability of systems that translate with fidelity interferon messenger RNA isolated from induced cells should prove most useful in the elucidation of post-transcriptional control mechanisms of interferon synthesis and of interferon superinduction. Meanwhile, superinduction has become a useful tool for the production of large quantities of interferon. In particular, this technique has been successfully applied to the production of interferon from human diploid fibroblasts. The clinical potential of this material remains to be critically examined.

摘要

自环己酰亚胺首次被证明能增强内毒素诱导的小鼠干扰素产生以来,已经过去了十年,这是后来被称为干扰素超诱导现象的首次证明。各种蛋白质和RNA合成抑制剂,以及这些抑制剂的组合,已被证明可作为聚肌苷酸-聚胞苷酸刺激的干扰素产生的超诱导剂。超诱导是由于抑制了干扰素合成的转录后调节机制这一证据相当有说服力。这种修饰是由一种蛋白质“阻遏物”引起的这一观点(大约六年前首次提出)仍然是最合理的假设,尽管尚未得到证实。能够准确翻译从诱导细胞中分离出的干扰素信使RNA的系统,对于阐明干扰素合成的转录后控制机制和干扰素超诱导现象应该是非常有用的。与此同时,超诱导已成为生产大量干扰素的一种有用工具。特别是,这项技术已成功应用于从人类二倍体成纤维细胞生产干扰素。这种物质的临床潜力仍有待严格审查。

相似文献

1
Superinduction of interferon with metabolic inhibitors: possible mechanisms and practical applications.用代谢抑制剂超诱导干扰素:可能的机制及实际应用
J Infect Dis. 1976 Jun;133 Suppl:A22-9. doi: 10.1093/infdis/133.supplement_2.a22.
2
The effects of some different metabolic inhibitors on interferon superinduction.某些不同代谢抑制剂对干扰素超诱导的影响。
J Gen Virol. 1978 Nov;41(2):229-37. doi: 10.1099/0022-1317-41-2-229.
3
Repeated 'superinduction' of interferon in human diploid fibroblast cultures.人二倍体成纤维细胞培养中干扰素的重复“超诱导”
J Gen Virol. 1977 Oct;37(1):221-3. doi: 10.1099/0022-1317-37-1-221.
4
[Interferon superinduction].
Postepy Hig Med Dosw. 1981 Jan-Feb;35(1):53-74.
5
[Interferon superinduction].[干扰素超诱导]
Antibiotiki. 1977 Oct;22(10):946-55.
6
Regulation of cellular interferon production: enhancement by antimetabolites.细胞干扰素产生的调节:抗代谢物的增强作用。
Proc Natl Acad Sci U S A. 1970 Sep;67(1):464-71. doi: 10.1073/pnas.67.1.464.
7
[Stimulation of interferon production].[干扰素生成的刺激]
Antibiotiki. 1979 Sep;24(9):669-72.
8
The influence of inhibitors of cellular synthesis and UV irradiation on interferon induction by RNA from Piptoporus betulinus.细胞合成抑制剂和紫外线照射对桦褐孔菌RNA诱导干扰素的影响。
Arch Immunol Ther Exp (Warsz). 1982;30(1-2):25-31.
9
Regulation of human interferon production. I. Superinduction by 5, 6-dichloro-1-beta-D-ribofuranosylbenzimidazole.人类干扰素产生的调控。I. 5,6-二氯-1-β-D-呋喃核糖基苯并咪唑的超诱导作用
Virology. 1976 Apr;70(2):532-41. doi: 10.1016/0042-6822(76)90294-4.
10
Enhancement of human interferon production by neutral red and chloroquine: analysis of inhibition of protein degradation and macromolecular synthesis.中性红和氯喹对人干扰素产生的增强作用:蛋白质降解抑制和大分子合成分析
J Exp Med. 1975 Nov 1;142(5):1283-1300. doi: 10.1084/jem.142.5.1283.

引用本文的文献

1
Use of gnotobiotic mice to identify and characterize key microbes responsible for the development of the intestinal immune system.使用无菌小鼠来识别和表征负责肠道免疫系统发育的关键微生物。
Proc Jpn Acad Ser B Phys Biol Sci. 2014;90(9):313-32. doi: 10.2183/pjab.90.313.
2
Cell-produced viral inhibitor: possible mechanism of action and chemical composition.细胞产生的病毒抑制剂:可能的作用机制和化学成分。
Infect Immun. 1981 May;32(2):454-7. doi: 10.1128/iai.32.2.454-457.1981.
3
Kinetics of decay in the expression of interferon-dependent mRNAs responsible for resistance to virus.
负责抗病毒的干扰素依赖性mRNA表达的衰减动力学。
Proc Natl Acad Sci U S A. 1980 Jan;77(1):452-6. doi: 10.1073/pnas.77.1.452.
4
Analysis of interferon mRNA in human fibroblast cells induced to produce interferon.对诱导产生干扰素的人成纤维细胞中干扰素信使核糖核酸的分析。
Proc Natl Acad Sci U S A. 1981 Dec;78(12):7426-30. doi: 10.1073/pnas.78.12.7426.
5
Antiviral agents: an update--Part 2.抗病毒药物:最新进展——第2部分。
Indian J Pediatr. 1980 Nov-Dec;47(389):515-22. doi: 10.1007/BF02822541.
6
Induction and regulation of mRNA encoding 26-kDa protein in human cell lines treated with recombinant human tumor necrosis factor.重组人肿瘤坏死因子处理的人细胞系中编码26 kDa蛋白的mRNA的诱导与调控
Proc Natl Acad Sci U S A. 1987 Jul;84(13):4557-61. doi: 10.1073/pnas.84.13.4557.
7
Interferon production in L929 cells under impaired translational conditions: comparison of rates of interferon, actin, Newcastle disease and encephalomyocarditis viruses mRNAs initiation of protein synthesis.翻译条件受损时L929细胞中干扰素的产生:干扰素、肌动蛋白、新城疫病毒和脑心肌炎病毒mRNA蛋白质合成起始速率的比较
Arch Virol. 1986;88(3-4):175-87. doi: 10.1007/BF01310873.
8
Interferon induction with Newcastle disease virus in FS-4 cells: effect of 5,6-dichloro-1-beta-D-ribofuranosylbenzimidazole (DRB).新城疫病毒在FS-4细胞中诱导干扰素:5,6-二氯-1-β-D-呋喃核糖基苯并咪唑(DRB)的作用
Arch Virol. 1979;62(3):263-71. doi: 10.1007/BF01317558.
9
Modified polyriboinosinic-polyribocytidylic acid complex: sustained interferonemia and its physiological associates in humans.修饰的聚肌苷酸-聚胞苷酸复合物:人类持续性干扰素血症及其生理相关因素
Infect Immun. 1979 Sep;25(3):831-7. doi: 10.1128/iai.25.3.831-837.1979.
10
Induction and decay of human fibroblast interferon mRNA.人成纤维细胞干扰素mRNA的诱导与衰减
Proc Natl Acad Sci U S A. 1977 Oct;74(10):4415-9. doi: 10.1073/pnas.74.10.4415.