发布: 2018年08月05日第8卷第15期 DOI: 10.21769/BioProtoc.2949 浏览次数: 5541
评审: David PaulJose Antonio Reyes-DariasAnonymous reviewer(s)
相关实验方案
利用小鼠Phospho-RTK Array试剂盒无偏筛选肿瘤提取物中激活受体酪氨酸激酶
Julian Naipauer [...] Enrique A. Mesri
2019年04月20日 4976 阅读
Abstract
Hepatitis C virus (HCV) spread involves two distinct entry pathways: cell-free transmission and cell-to-cell transmission. Cell-to-cell transmission is not only an efficient way for viruses to spread but also an effective method for escaping neutralizing antibodies. We adapted the viral infection-activated split-intein-mediated reporter system (VISI) and developed a straightforward model for Live-cell monitoring of HCV cell-to-cell transmission ex-vivo: co-culture of HCV infected donor cells (red signal) with uninfected recipient cells (green signal) and elimination of the cell-free transmission by adding potent neutralizing antibody AR3A in the supernatant. With this model, the efficiency of cell-to-cell transmission can be evaluated by counting the number of foci designated by the green signal of recipient cells.
Keywords: HCV (HCV)Background
Accumulating evidence support that viruses can use different routes of spread in infected tissues (Sattentau, 2008; Zhong et al., 2013). For HCV transmission, both cell-free transmission and cell-to-cell transmission can mediate virus transfer between hepatocytes. While cell-free transmission initiates HCV infection, cell-cell transmission is thought to transfer HCV to adjacent hepatocytes directly. It provides an excellent way to resist the neutralizing antibodies and contribute to the viral persistence (Brimacombe et al., 2011; Xiao et al., 2014). Previous articles also proved some host factors which contributed to cell-cell transmission, such as scavenger receptor BI (SR-BI), CD81, tight junction proteins claudin-1 (CLDN1), Occludin (OCLN), epidermal growth factor receptor (EGFR) (Witteveldt et al., 2009; Catanese et al., 2013; Zona et al., 2013). But the exact mechanisms of this process still need to explore. We optimized a viral infection-activated split-intein-mediated reporter system (VISI) for live-cell visualization of HCV infection (Zhao et al., 2017). Based on the study in Huh7.5.1 cell line using a technique of split GFP/RFP reconstitution by intein protein splicing (Figure 1A), it showed that VISI system is a very sensitive and low background system. With this system, we can clearly visualize the HCV infected cell by its nuclear fluorescence signal. In addition, combining VISI-GFP and VISI-mCherry cells, we can further monitor HCV cell-to-cell transmission in the presence of potent neutralizing antibody AR3A.
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版权信息
© 2018 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Zhao, F., Zhao, T., Deng, L., Lv, D., Zhang, X., Pan, X., Xu, J. and Long, G. (2018). HCV Reporter System (Viral Infection-Activated Split-Intein-Mediated Reporter System) for Testing Virus Cell-to-cell Transmission ex-vivo. Bio-protocol 8(15): e2949. DOI: 10.21769/BioProtoc.2949.
分类
微生物学 > 体内实验模型 > 病毒
细胞生物学 > 细胞成像 > 活细胞成像
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