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金纳米颗粒通过影响细胞器动态来对抗包膜 RNA 病毒。

Gold nanoparticles combat enveloped RNA virus by affecting organelle dynamics.

机构信息

CAS Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety, CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology of China, No. 11, First North Road, Zhongguancun, 100190, Beijing, P. R. China.

University of Chinese Academy of Sciences, 100049, Beijing, P. R. China.

出版信息

Signal Transduct Target Ther. 2023 Aug 2;8(1):285. doi: 10.1038/s41392-023-01562-w.

Abstract

Enveloped RNA viruses are a group of viruses with an outer membrane derived from a host cell and a genome consisting of ribonucleic acid (RNA). These viruses rely on host cell machinery and organelles to replicate and assemble new virus particles. However, the interaction between viruses and host organelles may be disrupted by nanomaterials, such as gold nanoparticles (AuNPs) with unique physical and chemical properties. In this study, we investigated the effects of AuNPs with different surface charge properties on the subcellular structure and function of mammalian cells, and their effects on two representative enveloped RNA viruses: lentivirus and human coronavirus OC43 (HCoV- OC43) antiviral potential. By comparing the subcellular effects of AuNPs with different surface charge properties, we found that treatment with AuNPs with positive surface charges induced more significant disruption of subcellular structures than neutrally charged AuNPs and negatively charged AuNPs, mainly manifested in lysosomes and Cytoskeletal disorders. The antiviral effect of the surface positively charged AuNPs was further evaluated using lentivirus and HCoV-OC43. The results showed that AuNPs had a significant inhibitory effect on both lentivirus and HCoV-OC43 without obvious side effects. In conclusion, our study provides insights into the mechanism of action and biocompatibility of AuNP in biological systems, while supporting the potential of targeting organelle dynamics against enveloped RNA viruses.

摘要

包膜 RNA 病毒是一组具有源自宿主细胞的外膜和由核糖核酸 (RNA) 组成的基因组的病毒。这些病毒依赖宿主细胞机制和细胞器来复制和组装新的病毒颗粒。然而,病毒与宿主细胞器之间的相互作用可能会被具有独特物理和化学性质的纳米材料(如金纳米粒子(AuNPs))所破坏。在这项研究中,我们研究了具有不同表面电荷特性的 AuNPs 对哺乳动物细胞亚细胞结构和功能的影响,以及它们对两种代表性包膜 RNA 病毒:慢病毒和人冠状病毒 OC43(HCoV-OC43)的抗病毒潜力的影响。通过比较具有不同表面电荷特性的 AuNPs 的亚细胞效应,我们发现带正电荷的 AuNPs 的处理比带中性电荷的 AuNPs 和带负电荷的 AuNPs 更能显著破坏亚细胞结构,主要表现为溶酶体和细胞骨架紊乱。使用慢病毒和 HCoV-OC43 进一步评估了带正电荷的 AuNPs 的抗病毒作用。结果表明,AuNPs 对慢病毒和 HCoV-OC43 均具有显著的抑制作用,而没有明显的副作用。总之,我们的研究提供了关于 AuNP 在生物系统中的作用机制和生物相容性的见解,同时支持针对包膜 RNA 病毒的细胞器动力学靶向的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d58/10393956/c83111dc1cd1/41392_2023_1562_Fig1_HTML.jpg

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