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抗艾滋病化合物聚肌苷酸-聚胞苷酸十二烷尿苷(Ampligen)的作用模式:2',5'-寡腺苷酸合成酶和双链RNA依赖性激酶的激活剂

Mode of action of the anti-AIDS compound poly(I).poly(C12U) (Ampligen): activator of 2',5'-oligoadenylate synthetase and double-stranded RNA-dependent kinase.

作者信息

Ushijima H, Rytik P G, Schäcke H, Scheffer U, Müller W E, Schröder H C

机构信息

Division of AIDS Virus, AIDS Research Center, National Institute of Health, Tokyo, Japan.

出版信息

J Interferon Res. 1993 Apr;13(2):161-71. doi: 10.1089/jir.1993.13.161.

Abstract

The mismatched double-stranded RNA (dsRNA), poly(I).poly(C12U), also termed Ampligen, exhibits a strong antiviral and cytoprotective effect on cells (human T-lymphoblastoid CEM cells and human T-cell line H9) infected with the human immunodeficiency virus type 1 (HIV-1). Untreated H9 cells infected with HIV-1 start to release the virus 3 days post-infection, while in the presence of 40 micrograms/ml (80 micrograms/ml) of poly(I).poly(C12U) the onset of virus production and release is retarded and does not occur before day 5 (day 6). We demonstrate that poly(I).poly(C12U) markedly extends the duration of the transient increase of 2',5'-oligoadenylate (2-5A) synthetase mRNA level and activity preceding virus production after infection of cells with HIV-1. Treatment of HeLa cells with poly(I).poly(C12U) was found to cause a significant increase in total (activated plus latent) 2-5A synthetase activity; no evidence was obtained that the level of latent (nonactivated) 2-5A synthetase is changed in cells treated with dsRNA plus interferon (IFN). Poly(I).poly(C12U) is able to bind and to activate 2-5A synthetase(s) from HeLa cell extracts. Addition of poly(I).poly(C12U) to HeLa cell extracts results in production of longer 2-5A oligomers (> or = 3 adenylate residues), which are better activators of RNase L. Both free and immobilized poly(I).poly(C12U) also bind to the dsRNA-dependent protein kinase (p68 kinase), resulting in autophosphorylation of the enzyme. Activation of the kinase by the free RNA occurs within a limited concentration range (10(-7) to 10(-6) grams/ml). Addition of HIV-1 Tat protein does not affect binding and activation of p68 kinase to poly(I).poly(C12U)-cellulose but strongly reduces the binding of the kinase to immobilized TAR RNA of HIV-1. We conclude that poly(I).poly(C12U) may antagonize Tat-mediated down-regulation of dsRNA-dependent enzymes.

摘要

错配双链RNA(dsRNA),即聚肌苷酸-聚胞苷酸12尿苷酸[poly(I).poly(C12U)],也称为Ampligen,对感染1型人类免疫缺陷病毒(HIV-1)的细胞(人T淋巴母细胞CEM细胞和人T细胞系H9)具有强大的抗病毒和细胞保护作用。未处理的感染HIV-1的H9细胞在感染后3天开始释放病毒,而在存在40微克/毫升(80微克/毫升)聚肌苷酸-聚胞苷酸12尿苷酸的情况下,病毒产生和释放的起始被延迟,直到第5天(第6天)才会发生。我们证明,聚肌苷酸-聚胞苷酸12尿苷酸显著延长了HIV-1感染细胞后病毒产生前2',5'-寡腺苷酸(2-5A)合成酶mRNA水平和活性短暂升高的持续时间。用聚肌苷酸-聚胞苷酸12尿苷酸处理HeLa细胞后,发现总(活化加潜伏)2-5A合成酶活性显著增加;没有证据表明在dsRNA加干扰素(IFN)处理的细胞中潜伏(未活化)2-5A合成酶的水平发生了变化。聚肌苷酸-聚胞苷酸12尿苷酸能够结合并激活HeLa细胞提取物中的2-5A合成酶。向HeLa细胞提取物中添加聚肌苷酸-聚胞苷酸12尿苷酸会产生更长的2-5A寡聚物(≥3个腺苷酸残基),它们是核糖核酸酶L更好的激活剂。游离的和固定化的聚肌苷酸-聚胞苷酸12尿苷酸也会与dsRNA依赖性蛋白激酶(p68激酶)结合,导致该酶的自身磷酸化。游离RNA对激酶的激活发生在有限的浓度范围内(10^-7至10^-6克/毫升)。添加HIV-1 Tat蛋白不会影响p68激酶与聚肌苷酸-聚胞苷酸12尿苷酸-纤维素的结合和激活,但会强烈降低该激酶与HIV-1固定化TAR RNA的结合。我们得出结论,聚肌苷酸-聚胞苷酸12尿苷酸可能拮抗Tat介导的dsRNA依赖性酶的下调。

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