淋巴毒素
淋巴毒素β受体
调解人
单纯疱疹病毒
细胞生物学
生物
跨膜蛋白
受体
肿瘤坏死因子α
淋巴毒素α
病毒学
分子生物学
病毒
免疫学
生物化学
作者
Davide Mauri,Reinhard Ebner,Rebecca I. Montgomery,Kristine D Kochel,Timothy C. Cheung,Guoliang Yu,Steve Ruben,Marianne Murphy,Roselyn J. Eisenberg,Gary H. Cohen,Patricia G. Spear,Carl F. Ware
出处
期刊:Immunity
[Cell Press]
日期:1998-01-01
卷期号:8 (1): 21-30
被引量:765
标识
DOI:10.1016/s1074-7613(00)80455-0
摘要
Herpes simplex virus (HSV) 1 and 2 infect activated T lymphocytes by attachment of the HSV envelope glycoprotein D (gD) to the cellular herpesvirus entry mediator (HVEM), an orphan member of the tumor necrosis factor receptor superfamily. Here, we demonstrate that HVEM binds two cellular ligands, secreted lymphotoxin α (LTα) and LIGHT, a new member of the TNF superfamily. LIGHT is a 29 kDa type II transmembrane protein produced by activated T cells that also engages the receptor for the LTαβ heterotrimer but does not form complexes with either LTα or LTβ. HSV1 gD inhibits the interaction of HVEM with LIGHT, and LIGHT and gD interfere with HVEM-dependent cell entry by HSV1. This characterizes herpesvirus gD as a membrane-bound viokine and establishes LIGHT-HVEM as integral components of the lymphotoxin cytokine-receptor system.8 These authors made equal contributions.
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