Sainteny F, Dumenil D, Frindel E
Leuk Res. 1984;8(2):285-93. doi: 10.1016/0145-2126(84)90152-8.
A single injection of 20 mg of Ara-C to mice provokes an acceleration of splenic CFU-S differentiation, followed by their entry in DNA synthesis. In this protocol, splenic CFU-S are induced to differentiate preferentially towards erythropoiesis. The present studies show that substances secreted by spleen cells from Ara-C treated mice are responsible for the modifications in the splenic CFU-S population. This indicates that splenic CFU-S kinetics is under the control of pluripoietins as previously demonstrated for marrow CFU-S. The serum of Ara-C treated mice is shown to have stimulating effects on splenic CFU-S as well as on medullary CFU-S proliferation. It also has the capacity of channelling the differentiation of both splenic and medullar CFU-S towards erythroid lineage. These data suggest the existence of long-range humoral regulators for both populations of CFU-S.
给小鼠单次注射20毫克阿糖胞苷会促使脾集落形成单位-脾(CFU-S)的分化加速,随后它们进入DNA合成阶段。在此实验方案中,脾CFU-S被诱导优先向红细胞生成方向分化。目前的研究表明,经阿糖胞苷处理的小鼠脾细胞分泌的物质是造成脾CFU-S群体变化的原因。这表明脾CFU-S的动力学受多能集落刺激因子的控制,正如先前对骨髓CFU-S所证明的那样。经阿糖胞苷处理的小鼠血清对脾CFU-S以及骨髓CFU-S的增殖具有刺激作用。它还具有引导脾和骨髓CFU-S向红细胞系分化的能力。这些数据表明这两种CFU-S群体都存在远程体液调节因子。