Greenberg P L, Mosny S A
Cancer Res. 1977 Jun;37(6):1794-9.
We have utilized in vitro marrow culture techniques to evaluate the cytotoxicity for granulocytic progenitor cells of two highly purified human leukocyte interferon preparations. Concentration- and time-related decrements in granulocytic colony-forming capacity in agar occurred with human and mouse marrow. Although mouse marrow cells were less sensitive than were human cells, these data indicate lack of strict species specificity for the cell growth-inhibitory effects of interferon. Similar cytotoxicity was noted for normal and leukemic human clonogenic cells exposed to interferon for prolonged periods. The decrease in the proportion of granulocytic progenitor cells in DNA synthesis, which occurred at high concentrations, and the diminution by interferon of the cytotoxicity caused by cytosine arabinoside demonstrate that interferon decreases DNA synthesis of granulocytic progenitor cells. The lack of enhanced cytotoxicity for rapidly proliferating mouse post-endotoxin marrow cells indicates that interferon is not a cell cycle-stage-specific drug. These data seem useful for evaluating the suppressive effects of interferon on granulopoiesis and for devising clinical trials with this agent.
我们利用体外骨髓培养技术评估了两种高度纯化的人白细胞干扰素制剂对粒细胞祖细胞的细胞毒性。人骨髓和小鼠骨髓在琼脂中的粒细胞集落形成能力出现了与浓度和时间相关的下降。虽然小鼠骨髓细胞比人细胞敏感性低,但这些数据表明干扰素对细胞生长的抑制作用缺乏严格的物种特异性。长时间暴露于干扰素的正常和白血病人类克隆细胞也观察到了类似的细胞毒性。高浓度时粒细胞祖细胞DNA合成比例下降,且干扰素减弱了阿糖胞苷引起的细胞毒性,这表明干扰素降低了粒细胞祖细胞的DNA合成。对快速增殖的小鼠内毒素后骨髓细胞缺乏增强的细胞毒性表明干扰素不是细胞周期阶段特异性药物。这些数据似乎有助于评估干扰素对粒细胞生成的抑制作用,并有助于设计使用该药物的临床试验。