Olson J K, Santos R A, Grose C
Departments of Microbiology and Pediatrics, University of Iowa College of Medicine, Iowa City, USA.
J Infect Dis. 1998 Nov;178 Suppl 1:S2-6. doi: 10.1086/514255.
Varicella-zoster virus (VZV) encodes a functional cell membrane Fc receptor called glycoprotein gE. VZV gE resembles other mammalian cell membrane receptors, such as the mammalian Fc receptor. In further analyses by transient transfection, the cellular trafficking of VZV gE was compared to other cell surface receptors. VZV gE was shown to undergo endocytosis from the cell membrane when visualized by laser scanning confocal microscopy. The endocytosis and trafficking pathway of VZV gE followed closely the pathway defined for the human transferrin receptor. Receptor-mediated endocytosis of VZV gE was dependent on a YAGL motif in its cytoplasmic tail. In addition, VZV gE underwent receptor-mediated endocytosis when it bound the Fc portion of immunoglobulin. Thus, this detailed study of VZV gE cellular trafficking has revealed potential roles for gE during viral infection.
水痘带状疱疹病毒(VZV)编码一种名为糖蛋白gE的功能性细胞膜Fc受体。VZV gE类似于其他哺乳动物细胞膜受体,如哺乳动物Fc受体。在通过瞬时转染进行的进一步分析中,将VZV gE的细胞运输与其他细胞表面受体进行了比较。通过激光扫描共聚焦显微镜观察发现,VZV gE可从细胞膜发生内吞作用。VZV gE的内吞和运输途径与人类转铁蛋白受体所定义的途径密切相关。VZV gE的受体介导内吞作用依赖于其细胞质尾部的YAGL基序。此外,当VZV gE与免疫球蛋白的Fc部分结合时,它会发生受体介导的内吞作用。因此,对VZV gE细胞运输的这项详细研究揭示了gE在病毒感染过程中的潜在作用。