Chung S W, Ruscetti S, Wong P M
Laboratory of Genetics, National Cancer Institute, Bethesda, MD 20892.
Blood. 1988 Apr;71(4):973-7.
Yolk-sac-derived hematopoietic cells were infected with a helper-free stock of Abelson virus (A-MuLV). After infection, cells were plated in a clonogenic methylcellulose culture in the absence of exogenous growth factors such as interleukin 3 (IL 3) and erythropoietin (Epo). No colonies were observed in cultures without viral infection, whereas factor-independent colonies were consistently observed with virus-infected cultures. The number of colonies was linearly correlated with the number of cells plated. Erythroid-mix colonies consisting mostly of erythroblasts, macrophages, and mast cells could be observed. Tumorigenic, continuously growing mast cell lines could be generated at high frequency from these erythroid-mix colonies after they were initially passaged in the presence of an irradiated feeder layer for 4 to 8 weeks. Southern blot analysis of the DNA from five of these lines examined were all shown to contain integrated A-MuLV proviral DNA. These data are evidence that A-MuLV can directly infect embryonic multipotent hematopoietic progenitor cells and drive them to differentiate to various progeny cells without exogenous growth factors.
用无辅助病毒的阿贝尔森病毒(A-MuLV)株感染源自卵黄囊的造血细胞。感染后,将细胞接种于不含白细胞介素3(IL-3)和促红细胞生成素(Epo)等外源性生长因子的克隆形成甲基纤维素培养基中。未感染病毒的培养物中未观察到集落,而病毒感染的培养物中则始终观察到不依赖因子的集落。集落数量与接种的细胞数量呈线性相关。可以观察到主要由成红细胞、巨噬细胞和肥大细胞组成的红系混合集落。在最初在经辐照的饲养层存在的情况下传代4至8周后,这些红系混合集落能够高频产生致瘤性、持续生长的肥大细胞系。对检测的其中五个细胞系的DNA进行Southern印迹分析,结果均显示含有整合的A-MuLV前病毒DNA。这些数据证明A-MuLV可直接感染胚胎多能造血祖细胞,并在无外源性生长因子的情况下驱动它们分化为各种子代细胞。