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新合成蛋白质对干扰素引发活性的需求

Requirement of newly synthesized protein for the priming activity of interferon.

作者信息

Ito J, Suzuki J, Kobayashi S

出版信息

Jpn J Microbiol. 1975 Apr;19(2):87-95. doi: 10.1111/j.1348-0421.1975.tb00854.x.

DOI:10.1111/j.1348-0421.1975.tb00854.x
PMID:168422
Abstract

Pretreatment of mouse L cells with interferon (IF) enhanced IF production in response to polyinosinic-polycytidylic acid (poly I-poly C). Post-treatment of cells with IF caused no significant enhancement of IF production. The enhancing effect of IF pretreatment (priming) reached a maximum after incubation with IF (10 or 100 units/ml) for 4-6 hr at 37 C, but this effect was absent when the incubation was done at 4 C. Cells which were incubated for additional several hours at 37 C after IF pretreatment at 4 C did not develop the primed state nor the antiviral state. The presence of protein synthesis inhibitors during the IF pretreatment depressed, though not completely, the development of the primed state. The residual priming effect was lost when the cells were incubated with the inhibitors at 37 C for 2 hr before they were exposed to poly I-poly C. There was no significant difference in the binding rate of poly I-poly C to cells between IF-treated and untreated cells. The degradation rate of cell-bound poly I-poly C and its sensitivity to exogenous pancreatic ribonuclease in the pretreated cells were also similar to those in the untreated cells.

摘要

用干扰素(IF)预处理小鼠L细胞,可增强其对聚肌苷酸-聚胞苷酸(聚I-聚C)的IF产生。用IF对细胞进行后处理不会显著增强IF产生。IF预处理(致敏)的增强作用在37℃下与IF(10或100单位/毫升)孵育4至6小时后达到最大值,但在4℃下孵育时则没有这种作用。在4℃下进行IF预处理后于37℃再孵育数小时的细胞,既未形成致敏状态也未形成抗病毒状态。IF预处理期间存在蛋白质合成抑制剂时,虽未完全抑制,但会抑制致敏状态的形成。当细胞在暴露于聚I-聚C之前于37℃与抑制剂孵育2小时,残余的致敏作用就会消失。IF处理组和未处理组细胞之间,聚I-聚C与细胞的结合率没有显著差异。预处理细胞中细胞结合的聚I-聚C的降解率及其对外源胰核糖核酸酶的敏感性也与未处理细胞中的相似。

相似文献

1
Requirement of newly synthesized protein for the priming activity of interferon.新合成蛋白质对干扰素引发活性的需求
Jpn J Microbiol. 1975 Apr;19(2):87-95. doi: 10.1111/j.1348-0421.1975.tb00854.x.
2
Are cytotoxicity and interferon inducing activity of poly(I).poly(C) invariably linked in interferon-treated L cells.在经干扰素处理的L细胞中,聚肌苷酸-聚胞苷酸的细胞毒性和干扰素诱导活性总是相关联的吗?
J Gen Virol. 1975 Apr;27(1):35-44. doi: 10.1099/0022-1317-27-1-35.
3
Priming increases the amount of interferon mRNA in poly(rI).poly(rC)-treated L cells.引发作用增加了经聚肌苷酸-聚胞苷酸处理的L细胞中干扰素信使核糖核酸的量。
J Gen Virol. 1979 Nov;45(2):301-8. doi: 10.1099/0022-1317-45-2-301.
4
Altered cellular responses to interferon induction by poly I-poly C: priming and hyporesponsiveness in cells treated with interferon preparations.聚肌苷酸-聚胞苷酸对干扰素诱导的细胞反应改变:用干扰素制剂处理的细胞中的启动作用和低反应性
Arch Gesamte Virusforsch. 1973;43(3):273-83.
5
Priming: a nonantiviral function of interferon.引发作用:干扰素的一种非抗病毒功能。
J Virol. 1971 Jun;7(6):792-801. doi: 10.1128/JVI.7.6.792-801.1971.
6
Further evidences that priming is a non-antiviral function of interferon.进一步的证据表明,引发作用是干扰素的一种非抗病毒功能。
Acta Microbiol Acad Sci Hung. 1974;21(3-4):305-9.
7
Kinetic and metabolic studies on the priming effect of interferon in L cells.干扰素对L细胞引发效应的动力学和代谢研究。
Arch Immunol Ther Exp (Warsz). 1977;25(5):631-9.
8
Study of the priming effect of interferon in L cells. I. The primed interferon response and the kinetics of development of priming.L细胞中干扰素引发效应的研究。I. 引发的干扰素反应及引发作用的发展动力学。
Acta Virol. 1976 Dec;20(6):472-8.
9
Stabilization of interferon messenger RNA activity by treatment of cells with metabolic inhibitors and lowering of the incubation temperature.通过用代谢抑制剂处理细胞并降低孵育温度来稳定干扰素信使核糖核酸的活性。
Proc Natl Acad Sci U S A. 1973 Dec;70(12):3909-13. doi: 10.1073/pnas.70.12.3909.
10
Studies on the mechanism of the priming effect of interferon on interferon production by cell cultures exposed to poly(rI)-poly(rC).关于干扰素对暴露于聚肌苷酸-聚胞苷酸的细胞培养物中干扰素产生的启动效应机制的研究。
Infect Immun. 1973 Sep;8(3):309-16. doi: 10.1128/iai.8.3.309-316.1973.