Zhang Xin, Lim Keesiang, Qiu Yujia, Hazawa Masaharu, Wong Richard W
Division of Nano Life Science, Graduate School of Frontier Science Initiative, Kanazawa University, Kanazawa 920-1192, Japan.
WPI-Nano Life Science Institute, Kanazawa University, Kanazawa 920-1192, Japan.
Viruses. 2025 Jan 23;17(2):151. doi: 10.3390/v17020151.
Viruses frequently exploit the host's nucleocytoplasmic trafficking machinery to facilitate their replication and evade immune defenses. By encoding specialized proteins and other components, they strategically target host nuclear transport receptors (NTRs) and nucleoporins within the spiderweb-like inner channel of the nuclear pore complex (NPC), enabling efficient access to the host nucleus. This review explores the intricate mechanisms governing the nuclear import and export of viral components, with a focus on the interplay between viral factors and host determinants that are essential for these processes. Given the pivotal role of nucleocytoplasmic shuttling in the viral life cycle, we also examine therapeutic strategies aimed at disrupting the host's nuclear transport pathways. This includes evaluating the efficacy of pharmacological inhibitors in impairing viral replication and assessing their potential as antiviral treatments. Furthermore, we emphasize the need for continued research to develop targeted therapies that leverage vulnerabilities in nucleocytoplasmic trafficking. Emerging high-resolution techniques, such as advanced imaging and computational modeling, are transforming our understanding of the dynamic interactions between viruses and the NPC. These cutting-edge tools are driving progress in identifying novel therapeutic opportunities and uncovering deeper insights into viral pathogenesis. This review highlights the importance of these advancements in paving the way for innovative antiviral strategies.
病毒经常利用宿主的核质运输机制来促进其复制并逃避免疫防御。通过编码特殊蛋白质和其他成分,它们有策略地靶向核孔复合体(NPC)类似蜘蛛网的内部通道中的宿主核转运受体(NTR)和核孔蛋白,从而能够有效进入宿主细胞核。本综述探讨了控制病毒成分核输入和输出的复杂机制,重点关注病毒因子与宿主决定因素之间的相互作用,这些相互作用对这些过程至关重要。鉴于核质穿梭在病毒生命周期中的关键作用,我们还研究了旨在破坏宿主核运输途径的治疗策略。这包括评估药理抑制剂在损害病毒复制方面的功效,并评估其作为抗病毒治疗的潜力。此外,我们强调需要持续开展研究以开发利用核质运输漏洞的靶向疗法。新兴的高分辨率技术,如先进成像和计算建模,正在改变我们对病毒与NPC之间动态相互作用的理解。这些前沿工具正在推动识别新的治疗机会以及深入了解病毒发病机制方面取得进展。本综述强调了这些进展在为创新抗病毒策略铺平道路方面的重要性。