PILRα Is a Herpes Simplex Virus-1 Entry Coreceptor That Associates with Glycoprotein B

نویسندگان

  • Takeshi Satoh
  • Jun Arii
  • Tadahiro Suenaga
  • Jing Wang
  • Amane Kogure
  • Junji Uehori
  • Noriko Arase
  • Ikuo Shiratori
  • Shinya Tanaka
  • Yasushi Kawaguchi
  • Patricia G. Spear
  • Lewis L. Lanier
  • Hisashi Arase
چکیده

Glycoprotein B (gB) is one of the essential components for infection by herpes simplex virus-1 (HSV-1). Although several cellular receptors that associate with glycoprotein D (gD), such as herpes virus entry mediator (HVEM) and Nectin-1, have been identified, specific molecules that mediate HSV-1 infection by associating with gB have not been elucidated. Here, we found that paired immunoglobulin-like type 2 receptor (PILR) alpha associates with gB, and cells transduced with PILRalpha become susceptible to HSV-1 infection. Furthermore, HSV-1 infection of human primary cells expressing both HVEM and PILRalpha was blocked by either anti-PILRalpha or anti-HVEM antibody. Our results demonstrate that cellular receptors for both gB and gD are required for HSV-1 infection and that PILRalpha plays an important role in HSV-1 infection as a coreceptor that associates with gB. These findings uncover a crucial aspect of the mechanism underlying HSV-1 infection.

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عنوان ژورنال:
  • Cell

دوره 132  شماره 

صفحات  -

تاریخ انتشار 2008