Jennings S R, Lippe P A, Pauza K J, Spear P G, Pereira L, Tevethia S S
J Virol. 1987 Jan;61(1):104-12. doi: 10.1128/JVI.61.1.104-112.1987.
The kinetics of expression of the herpes simplex virus type 1-encoded major glycoprotein species gB, gC, gD, and gE on the surfaces of cells of murine, simian, and human origins were studied. Viable cells were stained with monoclonal antibodies specific for each species, and the levels expressed were determined by fluorescence flow cytometry. Differences were observed in both the kinetics and the levels of expression of individual glycoprotein species, depending upon the origin of the host cells. Glycoprotein gC was expressed early and at high levels in cells of murine and human origins, but late and at relatively low levels in simian cells. In contrast, gE was expressed at high levels in simian cells, but was not detectable until late in the infectious cycle in murine and human cells. The kinetics and levels of expression of gB were similar for all cells investigated, whereas gD, with high levels of expression in all cells late in infection, appeared on the surfaces of murine cells very early postinfection. This approach has allowed a simple quantitative method for comparing levels of glycoprotein expression.
研究了单纯疱疹病毒1型编码的主要糖蛋白gB、gC、gD和gE在鼠源、猴源和人源细胞表面的表达动力学。用针对每种糖蛋白的单克隆抗体对活细胞进行染色,并通过荧光流式细胞术测定表达水平。根据宿主细胞的来源,在单个糖蛋白的表达动力学和水平上均观察到差异。糖蛋白gC在鼠源和人源细胞中早期高表达,但在猴源细胞中晚期低表达。相反,gE在猴源细胞中高表达,但在鼠源和人源细胞的感染周期后期才检测到。所有研究细胞中gB的表达动力学和水平相似,而gD在感染后期在所有细胞中高表达,在鼠源细胞感染后很早就出现在细胞表面。这种方法提供了一种比较糖蛋白表达水平的简单定量方法。