Author/Authors :
Takeshi Satoh، نويسنده , , Jun Arii، نويسنده , , Tadahiro Suenaga، نويسنده , , Jing Wang، نويسنده , , Amane Kogure، نويسنده , , Junji Uehori، نويسنده , , Noriko Arase، نويسنده , , Ikuo Shiratori، نويسنده , , Shinya Tanaka، نويسنده , , Yasushi Kawaguchi، نويسنده , , Patricia G. Spear، نويسنده , , Lewis L. Lanier، نويسنده , , Hisashi Arase، نويسنده ,
Abstract :
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) α associates with gB, and cells transduced with PILRα become susceptible to HSV-1 infection. Furthermore, HSV-1 infection of human primary cells expressing both HVEM and PILRα was blocked by either anti-PILRα or anti-HVEM antibody. Our results demonstrate that cellular receptors for both gB and gD are required for HSV-1 infection and that PILRα 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.