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视黄酸在两种转化的人细胞系中诱导2',5'-寡腺苷酸合成酶。

Induction of 2',5'-oligoadenylate synthetase by retinoic acid in two transformed human cell lines.

作者信息

Bourgeade M F, Besançon F

出版信息

Cancer Res. 1984 Nov;44(11):5355-60.

PMID:6435868
Abstract

2',5'-Oligoadenylate (2-5A) synthetase, which polymerizes adenosine triphosphate into 2-5A, is induced upon treatment of cells with interferon (IFN) and is thought to be involved in its antiviral and anticellular action. We report here that retinoic acid (RA) enhanced the level of this enzyme in two human transformed cell lines, WISH and Namalva. Like IFN, RA induced 2-5A synthetase activity in a time- and dose-dependent manner. Addition of anti IFN-alpha, -IFN-beta, or -IFN-gamma antibodies to the medium concomitantly with RA did not prevent such induction; therefore, the effect of RA is clearly not mediated through the induction and externalization of IFN. Pretreatment of cells with actinomycin D inhibited 2-5A synthetase induction by RA, suggesting that RA increased the transcription of the 2-5A synthetase gene. In WISH cells, the growth of encephalomyocarditis virus was inhibited by RA treatment, which is consistent with the hypothesis that 2-5A synthetase plays an important role in the antiviral action of IFN, at least in encephalomyocarditis virus replication. When the anticellular effects of IFN and RA were compared to their ability to induce 2-5A synthetase activity in four human cell lines, there was no strict correlation between the amplitude of the enzyme activity induced and the extent of the antiproliferative effect. It is concluded that the 2-5A system is probably not the only pathway responsible for the antiproliferative effect of both substances. We further suggest that the induction of 2-5A synthetase by IFN and RA might be connected with at least some of the similarities observed between other biological effects of both compounds.

摘要

2',5'-寡腺苷酸(2-5A)合成酶可将三磷酸腺苷聚合成2-5A,在用干扰素(IFN)处理细胞时会被诱导产生,并且被认为参与了其抗病毒和抗细胞作用。我们在此报告,视黄酸(RA)可提高两种人转化细胞系WISH和Namalva中该酶的水平。与IFN一样,RA以时间和剂量依赖的方式诱导2-5A合成酶活性。在加入RA的同时向培养基中添加抗IFN-α、-IFN-β或-IFN-γ抗体并不能阻止这种诱导;因此,RA的作用显然不是通过IFN的诱导和外化介导的。用放线菌素D预处理细胞可抑制RA对2-5A合成酶的诱导,这表明RA增加了2-5A合成酶基因的转录。在WISH细胞中,RA处理可抑制脑心肌炎病毒的生长,这与2-5A合成酶至少在脑心肌炎病毒复制的抗病毒作用中起重要作用的假设一致。当比较IFN和RA在四种人细胞系中的抗细胞作用与其诱导2-5A合成酶活性的能力时,诱导的酶活性幅度与抗增殖作用程度之间没有严格的相关性。结论是,2-5A系统可能不是这两种物质抗增殖作用的唯一途径。我们进一步表明,IFN和RA对2-5A合成酶 的诱导可能与这两种化合物其他生物学效应之间观察到的至少一些相似性有关。

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