体内
病毒
生物物理学
体外
临床前影像学
自体荧光
甲型流感病毒
化学
细胞生物学
病毒学
荧光
生物
生物化学
光学
物理
生物技术
作者
Gaoju Pang,Yingying Zhang,Xiaoyong Wang,Huizhuo Pan,Xinyu Zhang,Yayang Li,Shufang Zhang,Chun‐Hua Yan,Ling‐Dong Sun,Hanjie Wang,Jin Chang
出处
期刊:Nano Today
[Elsevier BV]
日期:2021-08-11
卷期号:40: 101264-101264
被引量:25
标识
DOI:10.1016/j.nantod.2021.101264
摘要
Virus labeling is an ideal strategy to explore the interaction between virus and host cells. However, existed probes are limited in in vivo studies due to the poor imaging effects caused by tissue-depth and autofluorescence. Lanthanide-doped upconversion nanoparticles (UCNP) can be effectively excited in deeper bio-tissues, and its long fluorescence life-time is suitable for in vivo imaging using time-resolved luminescence imaging technology. In this study, lanthanide-doped UCNP was used to label viral envelope and nucleic acid, which could be used for in vitro and in vivo virus tracking. The in vitro results demonstrated that the UCNP-labeled Influenza A virus (UCNP-IAV) could be used for the study of virus internalization kinetics, and proved that the movement of UCNP labeled IAV was lysosome- and microtube-dependent. For in vivo study, pre-labeling and in situ labeling strategies were implemented to monitor the IAV infection. The results showed that the UCNP probe could provide high-quality images using time-gated strategy to effectively monitor the viral infection in vivo. Further, simultaneous tracking of IAV and adenovirus type-5 (Ad5) labeled by UCNP with different life-time was realized using time-resolved luminescence imaging technology. Hence, this paper provided a novel labeling method for virus tracking using UCNP, which was optimal to study the mechanism of virus infection in vitro and in vivo.
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