Marra M, Imagawa D T
J Natl Cancer Inst. 1976 Nov;57(5):1133-8. doi: 10.1093/jnci/57.5.1133.
Oncornavirus production differed quantitatively among four Gross virus-induced murine leukemia clones. To determine the proportion of cells in each clone that were producing virus particles, the cells were stained by indirect immunofluorescence with antiserum to Gross antigen. All four clones had the same percentage of cells positive for the presence of Gross antigens irrespective of their ability to produce virus particles. A direct correlation was observed between the amount of RNA tumor virus attached to the plasma membrane and agglutination by concanavalin A. The leukemia strain that produced the most virus also had the greatest degree of agglutination. Oncornavirus production was indirectly related to oncogenicity of the cells in vivo: The clones that produced the most virus were the least malignant. The interaction of the host and virus-producing cells was monitored during animal passage, and virus production decreased during animal passage whereas transplantability increased.
在四种格罗斯病毒诱导的小鼠白血病克隆中,肿瘤病毒的产生在数量上有所不同。为了确定每个克隆中产生病毒颗粒的细胞比例,用抗格罗斯抗原的抗血清通过间接免疫荧光对细胞进行染色。所有四个克隆中,无论其产生病毒颗粒的能力如何,对格罗斯抗原呈阳性的细胞百分比相同。观察到附着在质膜上的RNA肿瘤病毒数量与伴刀豆球蛋白A的凝集之间存在直接相关性。产生病毒最多的白血病株凝集程度也最高。肿瘤病毒的产生与体内细胞的致癌性间接相关:产生病毒最多的克隆恶性程度最低。在动物传代过程中监测宿主与产生病毒的细胞之间的相互作用,传代过程中病毒产生减少而移植性增加。