Fuchs Anja, Cella Marina, Giurisato Emanuele, Shaw Andrey S, Colonna Marco
Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
J Immunol. 2004 Apr 1;172(7):3994-8. doi: 10.4049/jimmunol.172.7.3994.
The poliovirus receptor (PVR) belongs to a large family of Ig molecules called nectins and nectin-like proteins, which mediate cell-cell adhesion, cell migration, and serve as entry receptors for viruses. It has been recently shown that human NK cells recognize PVR through the receptor DNAM-1, which triggers NK cell stimulation in association with beta(2) integrin. In this study, we show that NK cells recognize PVR through an additional receptor, CD96, or T cell-activated increased late expression (Tactile). CD96 promotes NK cell adhesion to target cells expressing PVR, stimulates cytotoxicity of activated NK cells, and mediates acquisition of PVR from target cells. Thus, NK cells have evolved a dual receptor system that recognizes nectins and nectin-like molecules on target cells and mediates NK cell adhesion and triggering of effector functions. As PVR is highly expressed in certain tumors, this receptor system may be critical for NK cell recognition of tumors.
脊髓灰质炎病毒受体(PVR)属于一个名为nectins和nectin样蛋白的免疫球蛋白分子大家族,它们介导细胞间粘附、细胞迁移,并作为病毒的进入受体。最近研究表明,人类自然杀伤细胞(NK细胞)通过受体DNAM-1识别PVR,该受体与β2整合素协同触发NK细胞刺激。在本研究中,我们发现NK细胞通过另一种受体CD96(又称T细胞激活后晚期增加表达分子,即Tactile)识别PVR。CD96促进NK细胞与表达PVR的靶细胞粘附,刺激活化NK细胞的细胞毒性,并介导从靶细胞获取PVR。因此,NK细胞进化出了一种双重受体系统,该系统识别靶细胞上的nectins和nectin样分子,并介导NK细胞粘附和效应功能的触发。由于PVR在某些肿瘤中高度表达,这种受体系统可能对NK细胞识别肿瘤至关重要。