Lin H S
Cell Tissue Kinet. 1980 Jul;13(4):395-401. doi: 10.1111/j.1365-2184.1980.tb00478.x.
We investigated the proliferative state of peritoneal exudate macrophage colony-forming cells (PE-CFC) by exposing them to [3H]thymidine with a high specific activity in vitro and by administering cytosine arabinoside and methotrexate in vivo. Since [3H]TdR had no appreciable killing effect on PE-CFC and since the drug treatment caused no reduction in the appearance of PE-CFC, we concluded that the majority of PE-CFC, if not all, are not in active cell cycle. The production of PE-CFC was, however, suppressed by the administration of nitrogen mustard, cyclophosphamide, BCNU and vinlastine.
我们通过在体外将腹膜渗出巨噬细胞集落形成细胞(PE-CFC)暴露于具有高比活性的[3H]胸苷,并在体内给予阿糖胞苷和甲氨蝶呤,来研究其增殖状态。由于[3H]TdR对PE-CFC没有明显的杀伤作用,且药物治疗并未导致PE-CFC的出现减少,我们得出结论,大多数(如果不是全部)PE-CFC不在活跃细胞周期中。然而,氮芥、环磷酰胺、卡氮芥和长春花碱的给药会抑制PE-CFC的产生。