Ginsberg A H, Monte W T, Johnson K P
J Virol. 1977 Jan;21(1):277-83. doi: 10.1128/JVI.21.1.277-283.1977.
The effect of cyclophosphamide on the growth of Vero, BSC-1, and HeLa cells in monolayer cultures was studied. By using hemocytometer counts and tritiated thymidine uptake as indicators of growth, it was found that cyclophosphamide significantly interfered with the metabolism of Vero and BSC-1 cells when sustained in Leibovitz medium. Vero cells and HeLa cells grown in Eagle medium were not affected by exposure to cyclophosphamide. Vaccinia virus replication in Vero cell monolayer cultures incubated with cyclophosphamide was markedly augmented, and this enhanced growth was reflected by virus quantitation techniques and metabolic studies using tritiated thymidine uptake. No difference in the distribution of infectious particles was found when cyclophosphamide-treated and control infected cultures were compared. Pathways other than through hepatic enzymes appear available to activate cyclophosphamide in vitro. These effects are dependent on both the cell type and the medium in which the cells are grown. Cyclophosphamide can facilitate vaccinia virus replication in vitro through metabolic interactions at the cellular level. The precise mechanisms underlying this effect require further study.
研究了环磷酰胺对单层培养的非洲绿猴肾细胞(Vero)、非洲绿猴肾传代细胞(BSC - 1)和人宫颈癌细胞(HeLa)生长的影响。以血细胞计数器计数和氚标记胸腺嘧啶核苷摄取作为生长指标,发现当环磷酰胺持续存在于莱博维茨培养基中时,它会显著干扰Vero和BSC - 1细胞的代谢。在伊格尔培养基中生长的Vero细胞和HeLa细胞不受环磷酰胺暴露的影响。在用环磷酰胺孵育的Vero细胞单层培养物中,痘苗病毒的复制明显增强,这种生长增强通过病毒定量技术和使用氚标记胸腺嘧啶核苷摄取的代谢研究得以体现。比较经环磷酰胺处理的感染培养物和对照感染培养物时,未发现感染性颗粒分布有差异。在体外,除了通过肝酶的途径外,似乎还有其他途径可激活环磷酰胺。这些效应取决于细胞类型以及细胞生长所处的培养基。环磷酰胺可通过细胞水平的代谢相互作用促进体外痘苗病毒的复制。这种效应背后的确切机制需要进一步研究。