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MEAN通过干扰多嘧啶序列结合蛋白来抑制丙型肝炎病毒复制。

MEAN inhibits hepatitis C virus replication by interfering with a polypyrimidine tract-binding protein.

作者信息

Xue Jihua, Liu Yanning, Yang Ying, Wu Shanshan, Hu Ying, Yang Fan, Zhou Xiaotang, Wang Jing, Chen Feng, Zheng Min, Zhu Haihong, Chen Zhi

机构信息

State Key Lab of Diagnostic and Treatment of Infectious Diseases, Collaborative Innovation Center for Diagnosis and Treatment of Infectious Disease, 1st Affiliated Hospital of Medical School, Zhejiang University, Hangzhou, China.

出版信息

J Cell Mol Med. 2016 Jul;20(7):1255-65. doi: 10.1111/jcmm.12798. Epub 2016 Mar 1.

Abstract

MEAN (6-methoxyethylamino-numonafide) is a small molecule compound, and here, we report that it effectively inhibits hepatitis C virus (HCV) infection in an HCV cell culture system using a JC1-Luc chimeric virus, with a 50% effective concentration (EC50) of 2.36 ± 0.29 μM. Drug combination usage analyses demonstrated that MEAN was synergistic with interferon α, ITX5061 and ribavirin. In addition, MEAN effectively inhibits N415D mutant virus and G451R mutant viral infections. Mechanistic studies show that the treatment of HCV-infected hepatocytes with MEAN inhibits HCV replication but not translation. Furthermore, treatment with MEAN significantly reduces polypyrimidine tract-binding protein (PTB) levels and blocks the cytoplasmic redistribution of PTB upon infection. In the host cytoplasm, PTB is directly associated with HCV replication, and the inhibition of HCV replication by MEAN can result in the sequestration of PTB in treated nuclei. Taken together, these results indicate that MEAN is a potential therapeutic candidate for HCV infection, and the targeting of the nucleo-cytoplasmic translocation of the host PTB protein could be a novel strategy to interrupt HCV replication.

摘要

MEAN(6-甲氧基乙基氨基-努莫那非)是一种小分子化合物,在此我们报告,在使用JC1-Luc嵌合病毒的丙型肝炎病毒(HCV)细胞培养系统中,它能有效抑制HCV感染,半数有效浓度(EC50)为2.36±0.29μM。药物联合使用分析表明,MEAN与干扰素α、ITX5061和利巴韦林具有协同作用。此外,MEAN能有效抑制N415D突变病毒和G451R突变病毒感染。机制研究表明,用MEAN处理HCV感染的肝细胞可抑制HCV复制,但不抑制翻译。此外,用MEAN处理可显著降低多嘧啶序列结合蛋白(PTB)水平,并在感染时阻止PTB的细胞质重新分布。在宿主细胞质中,PTB与HCV复制直接相关,MEAN对HCV复制的抑制可导致PTB在处理后的细胞核中被隔离。综上所述,这些结果表明MEAN是HCV感染的潜在治疗候选药物,靶向宿主PTB蛋白的核质转运可能是中断HCV复制的一种新策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2722/4929307/c0a2c428b019/JCMM-20-1255-g001.jpg

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