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抗P-选择素糖蛋白配体-1抗体可阻断树突状细胞介导的肠道病毒71型传播,并预防病毒诱导的细胞死亡。

Antibodies to P-selectin glycoprotein ligand-1 block dendritic cell-mediated enterovirus 71 transmission and prevent virus-induced cells death.

作者信息

Ren Xiao-Xin, Li Chuan, Xiong Si-Dong, Huang Zhong, Wang Jian-Hua, Wang Hai-Bo

机构信息

a Jiangsu Key Laboratory of Infection and Immunity; Institutes of Biology and Medical Sciences; Soochow University ; Suzhou , China.

b Key Laboratory of Molecular Virology and Immunology; Institute Pasteur of Shanghai; Chinese Academy of Sciences ; Shanghai , China.

出版信息

Virulence. 2015;6(8):802-8. doi: 10.1080/21505594.2015.1094605. Epub 2015 Sep 23.

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.

摘要

P选择素糖蛋白配体-1(PSGL-1)已被证明是肠道病毒71型(EV71)的功能性受体。我们发现PSGL-1在单核细胞来源的树突状细胞(MDDC)上大量表达。然而,我们之前已经证明MDDC不支持EV71的有效复制。树突状细胞(DC)已被描述为被包括EV71在内的各种病毒颠覆以进行病毒传播,因此我们探索PSGL-1在DC介导的EV71传播中的潜在作用。我们发现MDDC上细胞表面表达的PSGL-1介导EV71结合,有趣的是,MDDC上这些负载病毒可以转移到遇到的靶细胞;用PSGL-1抗体预处理或干扰PSGL-1表达可减少MDDC介导的EV71转移并挽救病毒诱导的细胞死亡。我们的数据揭示了PSGL-1在DC介导的EV71传播中的新作用,并为阻断原发性EV71感染提供了见解。

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