Abstract
P-selectin glycoprotein ligand-1 (PSGL-1) has been proved to serve as the functional receptor for enterovirus 71 (EV71). We found the abundant expression of PSGL-1 on monocyte-derived dendritic cells (MDDCs). However, we have previously demonstrated that MDDCs did not support efficient replication of EV71. Dendritic cells (DCs) have been described to be subverted by various viruses including EV71 for viral dissemination, we thus explore the potential contribution of PSGL-1 on DC-mediated EV71 transmission. We found that the cell-surface-expressing PSGL-1 on MDDCs mediated EV71 binding, and intriguingly, these loaded-viruses on MDDCs could be transferred to encountered target cells; Prior-treatment with PSGL-1 antibodies or interference with PSGL-1 expression diminished MDDC-mediated EV71 transfer and rescued virus-induced cell death. Our data uncover a novel role of PSGL-1 in DC-mediated EV71 spread, and provide an insight into blocking primary EV71 infection.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 802-808 |
| Number of pages | 7 |
| Journal | Virulence |
| Volume | 6 |
| Issue number | 8 |
| DOIs | |
| State | Published - Jan 1 2015 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Dendritic cell
- Enterovirus 71
- P-selectin glycoprotein ligand-1
- Viral transmission
ASJC Scopus subject areas
- Parasitology
- Microbiology
- Immunology
- Microbiology (medical)
- Infectious Diseases
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