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紫外线照射兔细胞后干扰素的诱导作用。

Interferon induction in rabbit cells irradiated with UV light.

作者信息

Mozes L W, Vilcek J

出版信息

J Virol. 1974 Mar;13(3):646-51. doi: 10.1128/JVI.13.3.646-651.1974.

Abstract

UV irradiation of a continuous line of rabbit kidney cells (RK13) was used as a tool for the study of the mechanism of interferon induction. Irradiation of cells prior to their exposure to Newcastle disease virus (NDV) resulted in a dose-dependent decrease in interferon production. The inhibition of total cellular RNA synthesis by UV irradiation in uninduced cultures was similar to the inactivation curve of interferon production in NDV-induced cultures. In contrast, the production of interferon with polyinosinate-polycytidylate (poly[I].poly [C]) paradoxically was enhanced in cells irradiated with a wide range of doses of UV. However, in cells stimulated with poly(I).poly(C) and "superinduced" by the sequential addition of cycloheximide and actinomycin D, the rate of inactivation of interferon production by UV light was similar to that observed with NDV. These results are not inconsistent with the idea that both poly(I).poly(C) and NDV stimulate the same interferon gene(s), but indicate that the mechanism controlling its expression may be different for each inducer.

摘要

兔肾细胞连续系(RK13)的紫外线照射被用作研究干扰素诱导机制的工具。在细胞暴露于新城疫病毒(NDV)之前进行照射,会导致干扰素产生呈剂量依赖性减少。在未诱导的培养物中,紫外线照射对总细胞RNA合成的抑制作用与NDV诱导的培养物中干扰素产生的失活曲线相似。相比之下,用多聚肌苷酸-多聚胞苷酸(poly[I]·poly[C])诱导干扰素时,在广泛剂量的紫外线照射下,干扰素的产生反而增强。然而,在用poly(I)·poly(C)刺激并通过依次添加环己酰亚胺和放线菌素D进行“超诱导”的细胞中,紫外线使干扰素产生失活的速率与NDV诱导的情况相似。这些结果与poly(I)·poly(C)和NDV刺激相同的干扰素基因这一观点并不矛盾,但表明每种诱导剂控制其表达的机制可能不同。

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Post-transcriptional control of interferon synthesis.干扰素合成的转录后调控。
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本文引用的文献

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Interferon production in chick embryo cells. II. The role of DNA.
Virology. 1966 Jan;28(1):108-14. doi: 10.1016/0042-6822(66)90311-4.
6
Simultaneous viral and non-viral interferon production in human cell cultures.
Proc Soc Exp Biol Med. 1970 Mar;133(3):982-5. doi: 10.3181/00379727-133-34609.
7
A radiobiological study of the replication of Newcastle disease virus and of interferon formation in vitro.
Int J Radiat Biol Relat Stud Phys Chem Med. 1969;16(2):129-45. doi: 10.1080/09553006914551151.

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