Watanabe K, Takizawa N, Noda S, Tsukahara F, Maru Y, Kobayashi N
Laboratory of Molecular Biology of Infectious Agents, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki, Japan.
Drug Discov Ther. 2008 Apr;2(2):77-84.
In our previous report, we demonstrated that the matrix 1 (M1) protein of influenza virus directly binds to heat shock cognate protein 70 (Hsc70). The down-regulation of Hsc70 resulted in the reduction of influenza virus production, thus suggesting that Hsc70 plays a crucial role for viral replication. However, the detailed role of Hsc70 in viral replication remains to be elucidated. Hsc70 has been suggested to play a significant role in both the nuclear import and export processes. In this report, using leptomycin B (LMB), a CRM1-mediated nuclear export inhibitor, we demonstrated that Hsc70 forms a complex with vRNP through M1 in infected cells and in the virion, thus playing a significant role in the export of vRNP from the nucleus but not in the import of vRNP into the nucleus. The regulation of Hsc70 may therefore lead to the development of new anti-influenza virus drugs without raising mutant viruses.
在我们之前的报告中,我们证明了流感病毒的基质1(M1)蛋白直接与热休克同源蛋白70(Hsc70)结合。Hsc70的下调导致流感病毒产生减少,因此表明Hsc70对病毒复制起着关键作用。然而,Hsc70在病毒复制中的具体作用仍有待阐明。有人提出Hsc70在核输入和输出过程中都起着重要作用。在本报告中,我们使用CRM1介导的核输出抑制剂雷帕霉素B(LMB)证明,Hsc70在感染细胞和病毒体中通过M1与病毒核糖核蛋白(vRNP)形成复合物,因此在vRNP从细胞核输出中起重要作用,而在vRNP进入细胞核的过程中不起作用。因此,对Hsc70的调控可能会导致开发出新的抗流感病毒药物,而不会产生突变病毒。