Datta S K, Waksal S D, Schwartz R S
Cell. 1980 Jan;19(1):171-9. doi: 10.1016/0092-8674(80)90398-0.
(AKR x NZB)F1 mice possess the dominant genes, Akv-1, Akv-2, Nzv-1a and Nzv-2a, which determine the expression of ecotropic and xenotropic viruses. Nevertheless, their thymic lymphocytes fail to produce these agents, and these mice are resistant to leukemia. We investigated the mechanism of this cell-specific restriction in radiation chimeras. (AKR x NZB)F1 thymocytes that had differentiated in lethally irradiated AKR recipients produced high levels of ecotropic and xenotropic viruses and showed marked amplification of MuLV antigen expression. Polytropic viruses could also be isolated from such thymocytes. These virological changes in chimeric thymocytes were donor- and host-specific and occurred only when (AKR x NZB)F1 bone marrow cells were inoculated into AKR recipients. This inductive capacity of the host environment could be detected in irradiated AKR recipients as early as age 2 months. The phenotypic changes brought about in leukemia-resistant (AKR x NZB)F1 thymocytes by the leukemia-susceptible AKR thymic microenvironment may be the result of a three-component inductive system.
(AKR×NZB)F1小鼠携带显性基因Akv-1、Akv-2、Nzv-1a和Nzv-2a,这些基因决定嗜亲性病毒和异嗜性病毒的表达。然而,它们的胸腺淋巴细胞无法产生这些病毒,并且这些小鼠对白血病具有抗性。我们研究了辐射嵌合体中这种细胞特异性限制的机制。在接受致死剂量照射的AKR受体中分化的(AKR×NZB)F1胸腺细胞产生高水平的嗜亲性病毒和异嗜性病毒,并显示出MuLV抗原表达的显著扩增。多嗜性病毒也可从此类胸腺细胞中分离出来。嵌合胸腺细胞中的这些病毒学变化是供体和宿主特异性的,并且仅在将(AKR×NZB)F1骨髓细胞接种到AKR受体中时才会发生。宿主环境的这种诱导能力早在2月龄的受照射AKR受体中就能检测到。白血病易感的AKR胸腺微环境给抗白血病的(AKR×NZB)F1胸腺细胞带来的表型变化可能是一个三组分诱导系统的结果。