4.6 Article

Interaction between TIM-1 and NPC1 Is Important for Cellular Entry of Ebola Virus

Journal

JOURNAL OF VIROLOGY
Volume 89, Issue 12, Pages 6481-6493

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/JVI.03156-14

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Funding

  1. Grants-in-Aid for Scientific Research [25892002, 25115501, 25870017, 15H01249] Funding Source: KAKEN

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Multiple host molecules are known to be involved in the cellular entry of filoviruses, including Ebola virus (EBOV); T-cell immunoglobulin and mucin domain 1 (TIM-1) and Niemann-Pick C1 (NPC1) have been identified as attachment and fusion receptors, respectively. However, the molecular mechanisms underlying the entry process have not been fully understood. We found that TIM-1 and NPC1 colocalized and interacted in the intracellular vesicles where EBOV glycoprotein (GP)-mediated membrane fusion occurred. Interestingly, a TIM-1-specific monoclonal antibody (MAb), M224/1, prevented GP-mediated membrane fusion and also interfered with the binding of TIM-1 to NPC1, suggesting that the interaction between TIM-1 and NPC1 is important for filovirus membrane fusion. Moreover, MAb M224/1 efficiently inhibited the cellular entry of viruses from all known filovirus species. These data suggest a novel mechanism underlying filovirus membrane fusion and provide a potential cellular target for antiviral compounds that can be universally used against filovirus infections.

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