Johnson D C, Burke R L, Gregory T
Department of Pathology, McMaster University, Hamilton, Ontario, Canada.
J Virol. 1990 Jun;64(6):2569-76. doi: 10.1128/JVI.64.6.2569-2576.1990.
Herpes simplex virus type 1 (HSV-1) and HSV-2 plaque production was inhibited by treating cells with soluble forms of HSV-1 glycoprotein D (gD-1t) and HSV-2 glycoprotein D (gD-2t). Both glycoproteins inhibited entry of HSV-1 and HSV-2 without affecting virus adsorption. In contrast, a soluble form of HSV-2 glycoprotein B had no effect on virus entry into cells. Specific binding of gD-1t and gD-2t to cells was saturable, and approximately 4 x 10(5) to 5 x 10(5) molecules bound per cell. Binding of gD-1t was markedly reduced by treating cells with certain proteases but was unaffected when cell surface heparan sulfate glycosaminoglycans were enzymatically removed or when the binding was carried out in the presence of heparin. Together, these results suggest that gD binds to a limited set of cell surface receptors which may be proteins and that these interactions are essential for subsequent virus entry into cells. However, binding of gD to its receptors is not required for the initial adsorption of virus to the cell surface, which involves more numerous sites (probably including heparan sulfate) than those which mediate gD binding.
用单纯疱疹病毒1型(HSV-1)糖蛋白D(gD-1t)和单纯疱疹病毒2型(HSV-2)糖蛋白D(gD-2t)的可溶性形式处理细胞,可抑制HSV-1和HSV-2的蚀斑形成。两种糖蛋白均抑制HSV-1和HSV-2的进入,但不影响病毒吸附。相比之下,HSV-2糖蛋白B的可溶性形式对病毒进入细胞没有影响。gD-1t和gD-2t与细胞的特异性结合是可饱和的,每个细胞约有4×10⁵至5×10⁵个分子结合。用某些蛋白酶处理细胞可使gD-1t的结合显著减少,但当细胞表面硫酸乙酰肝素糖胺聚糖被酶解去除或在肝素存在下进行结合时,gD-1t的结合不受影响。这些结果共同表明,gD与一组有限的细胞表面受体结合,这些受体可能是蛋白质,并且这些相互作用对于随后病毒进入细胞至关重要。然而,病毒最初吸附到细胞表面并不需要gD与其受体结合,病毒吸附涉及的位点(可能包括硫酸乙酰肝素)比介导gD结合的位点更多。