de Both N J, Vermey M, van Griensven L J
Exp Hematol. 1978 Jun;6(6):515-27.
Cell proliferation was investigated in normal and Rauscher Leukemia Virus-infected BALB/c mice. Five days after inoculation, islands of leukemic blasts arose in the red pulp, and proliferated as shown by autoradiographic analysis after a pulse of 3H-Thymidine. These cells subsequently infiltrated the whole spleen and 3 weeks after infection about 60% of the spleen consisted of large immature erythroblast-like cells. Repeated injections of 3H-Thymidine led to uniform labeling of 85% of the spleen cells. Cell cycle analysis showed that for bone marrow as well as for spleen cells the total duration of the cell cycle did not differ from the cell cycle times of normal erythroblasts. From the difference between the actual doubling time and the potential doubling time (estimated on the basis of the cell cycle time) it can be calculated that considerable cell loss must occur. This cell loss is only to a minor extent due to the release of blasts into the peripheral blood. Probably cell death and extrusion of nuclei during erythroid differentiation are the main factors involved.
在正常和劳舍尔白血病病毒感染的BALB/c小鼠中研究了细胞增殖情况。接种五天后,红髓中出现白血病母细胞岛,并如经3H-胸腺嘧啶脉冲后的放射自显影分析所示进行增殖。这些细胞随后浸润整个脾脏,感染三周后,约60%的脾脏由大型未成熟成红细胞样细胞组成。重复注射3H-胸腺嘧啶导致85%的脾细胞均匀标记。细胞周期分析表明,骨髓和脾细胞的细胞周期总时长与正常成红细胞的细胞周期时长没有差异。根据实际倍增时间与潜在倍增时间(根据细胞周期时长估算)之间的差异,可以计算出必然发生了相当数量的细胞损失。这种细胞损失在很小程度上是由于母细胞释放到外周血中。可能细胞死亡和红细胞分化过程中细胞核的挤出是主要相关因素。