Kovacs C J, Evans M J, Roberts C, Harrell J, Abernathy R, Gooya J, Johnke R M
Department of Radiation Oncology, Leo Jenkins Cancer Center, East Carolina University School of Medicine, Greenville, NC 27858, USA.
Exp Hematol. 1995 Aug;23(9):1016-23.
Studies were carried out to establish the temporal effects of abbreviated administrations of IL-1 and IL-1 plus M-CSF as rescue agents on multipotential and short-term repopulating hematopoietic stem cell (HSC) subpopulations in murine marrow treated with a myelosuppressive dose of 150 mg/kg 5-FU. The recovery kinetics for high-proliferative-potential colony-forming cells (HPP-CFC), CFU-S8 and -S12, and both CFU-M and CFU-G compartments were monitored over a 14-day interval in 5-FU-treated bone marrow (FUBM) following daily cytokine injections over a 4-day interval. Both IL-1 and the coadministration of IL-1 and M-CSF rapidly enhanced the recovery of the HPP-CFC in FUBM to supranormal levels and maintained these levels for extended intervals. Moreover, since M-CSF was unable to influence the recovery of the HSC subpopulations in FUBM by itself, the results of the two cytokines amounted to a synergistic effect on the recovery of the HPP-CFC in FUBM and a reduction of severe neutropenia in the myelosuppressed animal. Scheduling studies demonstrated that these synergistic effects were restricted to those schedules in which M-CSF was coadministered with IL-1 during the first 2 days of cytokine rescue. Finally, the recovery curves generated for the HSC and CFU-M subpopulations in response to IL-1 (with or without M-CSF) also suggest that these cytokines may conceivably alter the normal balance between proliferation and differentiation within CFU-S8 and -S12 during the accelerated recovery of hematopoiesis in FUBM.
开展了多项研究,以确定将白细胞介素-1(IL-1)和IL-1加巨噬细胞集落刺激因子(M-CSF)作为救援剂进行短期给药,对用150mg/kg骨髓抑制剂量的5-氟尿嘧啶(5-FU)处理的小鼠骨髓中多能和短期再增殖造血干细胞(HSC)亚群的时间效应。在4天的间隔内每日注射细胞因子后,在14天的间隔内监测5-FU处理的骨髓(FUBM)中高增殖潜能集落形成细胞(HPP-CFC)、CFU-S8和-S12以及CFU-M和CFU-G区室的恢复动力学。IL-1以及IL-1与M-CSF联合给药均迅速将FUBM中HPP-CFC的恢复提高到超正常水平,并将这些水平维持较长时间。此外,由于M-CSF自身无法影响FUBM中HSC亚群的恢复,两种细胞因子的结果对FUBM中HPP-CFC的恢复产生协同作用,并减少了骨髓抑制动物的严重中性粒细胞减少。给药方案研究表明,这些协同效应仅限于在细胞因子救援的前2天将M-CSF与IL-1联合给药的方案。最后,针对HSC和CFU-M亚群响应IL-1(有或没有M-CSF)生成的恢复曲线也表明,在FUBM造血加速恢复期间,这些细胞因子可能会改变CFU-S8和-S12内增殖与分化之间的正常平衡。