Krzystyniak K, Dupuy J M
J Gen Virol. 1981 Nov;57(Pt 1):53-61. doi: 10.1099/0022-1317-57-1-53.
The interaction between mouse hepatitis virus 3 (MHV3) and cells was studied in order to investigate whether or not early events occurring after infection could be involved in the difference in virus replication seen between mouse strains with different genetic sensitivities to MHV3 infection. Kinetic data showed that MHV3 uptake by both macrophages and L cells was time- and temperature-dependent. In addition, treatment of cells with cytochalasin B or prostaglandin E1, prior to virus infection, resulted in a strong inhibition of sheep red blood cell phagocytosis without any effect on MHV3 uptake. Similar uptake of radiolabelled MHV3 was shown by whole spleen cells, purified T lymphocytes and thymocytes. Furthermore, no difference in 3H-labelled MHV3 uptake was seen between macrophages originating from resistant A/J mice, semi-susceptible (C57Bl/6 x A/J)F1 and susceptible animals. These results indicate, therefore, that genetically related in vivo sensitivity toward MHV3 infection is not related to differential uptake of virus by cells.
为了研究感染后早期事件是否与对MHV3感染具有不同遗传敏感性的小鼠品系之间观察到的病毒复制差异有关,对小鼠肝炎病毒3型(MHV3)与细胞之间的相互作用进行了研究。动力学数据表明,巨噬细胞和L细胞对MHV3的摄取均具有时间和温度依赖性。此外,在病毒感染前用细胞松弛素B或前列腺素E1处理细胞,会强烈抑制绵羊红细胞吞噬作用,而对MHV3摄取没有任何影响。全脾细胞、纯化的T淋巴细胞和胸腺细胞对放射性标记的MHV3的摄取情况相似。此外,来自抗性A/J小鼠、半易感(C57Bl/6×A/J)F1小鼠和易感动物的巨噬细胞对3H标记的MHV3的摄取没有差异。因此,这些结果表明,对MHV3感染的体内遗传相关性敏感性与细胞对病毒的差异摄取无关。