PT  - JOURNAL ARTICLE
AU  - Zhenlan Yao
AU  - Xiaofang Li
AU  - Jieliang Chen
AU  - Yunsheng Qiao
AU  - Fang Shen
AU  - Bisheng Shi
AU  - Jia Liu
AU  - Jiahui Ding
AU  - Lu Peng
AU  - Jianhua Li
AU  - Zhenghong Yuan
TI  - Exosomes exploit the virus entry machinery and pathway to transmit IFN-α-induced antiviral activity
AID  - 10.1101/300715
DP  - 2018 Jan 01
TA  - bioRxiv
PG  - 300715
4099  - http://biorxiv.org/content/early/2018/04/13/300715.short
4100  - http://biorxiv.org/content/early/2018/04/13/300715.full
AB  - Interferon-α (IFN-α) induces the transfer of resistance to hepatitis B virus (HBV) from liver nonparenchymal cells (LNPCs) to hepatocytes via exosomes. However, little is known about the entry machinery and pathway involved in the transmission of IFN-α-induced antiviral activity. Here, we found that macrophage exosomes depend on T cell immunoglobulin and mucin receptor 1 (TIM-1), a hepatitis A virus (HAV) receptor, to enter hepatocytes for delivering IFN-α-induced anti-HBV activity. Moreover, two primary endocytic routes for virus infection, clathrin-mediated endocytosis (CME) and macropinocytosis, collaborate to permit exosome entry and anti-HBV activity transfer. Subsequently, lysobisphosphatidic acid (LBPA), an anionic lipid closely related to endosome penetration of virus, facilitates membrane fusion of exosomes in late endosomes/ multivesicular bodies (LEs/MVBs) and the accompanying exosomal cargo uncoating. Together, this study provides comprehensive insights into the transmission route of macrophage exosomes to efficiently deliver IFN-α-induced anti-HBV activity and highlights the similarities between the entry mechanisms of exosomes and virus.Importance Our previous study showed that LNPC-derived exosomes could transmit IFN-α-induced antiviral activity to HBV replicating hepatocytes, but the concrete transmission mechanisms which include exosome entry and exosomal cargo release remain unclear. In this study, we found that virus entry machinery and pathway were also applied to exosome-mediated cell-to-cell antiviral activity transfer. Macrophage-derived exosomes exploit hepatitis A virus receptor for access to hepatocytes. Later, CME and macropinocytosis are utilized by exosomes which is followed by exosome-endosome fusion for efficient transfer of IFN-α-induced anti-HBV activity. Dissecting the similarities between exosome and virus entry will be beneficial to designing exosomes as efficient vehicles for antiviral therapy.