Zielinski C C, Waksal S D, Datta S K
J Immunol. 1982 Aug;129(2):882-9.
In the leukemia-prone AKR thymus, ecotropic and xenotropic-related viruses are expressed that generate leukemogenic recombinant viruses before the onset of leukemia. We have shown previously that (AKR X NZB)F1 hybrid mice do not develop leukemia because they severely restrict the expression of these retroviruses in their thymuses. The thymic microenvironment of the (AKR X NZB)F1 mice appeared to be of particular importance in determining this restriction, which was specified by an NZB-derived genetic influence. In the present study we analyze reciprocal thymus graft and irradiation bone marrow chimeras to establish that this influence is exerted by thymic reticuloepithelial cells. Prospective studies with thymic epithelial grafts from young mice show that the AKR thymic epithelium can simultaneously induce the amplified expression of retroviral genes, and changes in patterns of thymocyte differentiation that precede the development of leukemia, whereas the (AKR X NZB)F1 thymic epithelium is deficient in this regard.
在易患白血病的AKR小鼠胸腺中,嗜亲性和异嗜性相关病毒得以表达,这些病毒在白血病发作前产生致白血病重组病毒。我们之前已经表明,(AKR×NZB)F1杂交小鼠不会患白血病,因为它们严重限制了这些逆转录病毒在其胸腺中的表达。(AKR×NZB)F1小鼠的胸腺微环境在决定这种限制方面似乎尤为重要,这种限制是由NZB衍生的遗传影响所决定的。在本研究中,我们分析了相互胸腺移植和照射骨髓嵌合体,以确定这种影响是由胸腺网状上皮细胞施加的。对来自年轻小鼠的胸腺上皮移植进行的前瞻性研究表明,AKR胸腺上皮可同时诱导逆转录病毒基因的扩增表达,以及在白血病发生之前胸腺细胞分化模式的变化,而(AKR×NZB)F1胸腺上皮在这方面存在缺陷。