Vannucchi A M, Grossi A, Rafanelli D, Ferrini P R
Division of Hematology, University of Florence-USL 10/D, Italy.
Blood. 1990 Oct 15;76(8):1473-80.
Murine recombinant granulocyte-macrophage colony-stimulating factor (rGM-CSF) was injected in mice, and the effects on bone marrow, splenic megakaryocytes, megakaryocyte precursors (megakaryocyte colony-forming units [CFU-Meg]) were evaluated. In mice injected three times a day for 6 days with 12,000 to 120,000 U rGM-CSF, no significant modification of both platelet levels and mean platelet volume was observed, while there was a twofold increase in blood neutrophils. However, the rate of platelet production, as assessed by the measurement of 75selenomethionine incorporation into blood platelets, was On the contrary, administration of up to 384,000 U rGM-CSF two times a day for 2 days, as for a typical "thrombopoietin assay," failed to modify platelet production. A significant dose-related increase in the number of splenic megakaryocytes occurred in mice receiving 60,000 to 120,000 U rGM-CSF, while a slight increase in the number of bone marrow megakaryocytes was observed in mice injected with 120,000 U rGM-CSF. The proportion of bone marrow megakaryocytes with a size less than 18 microns and greater than 35 microns resulted significantly higher in mice receiving rGM-CSF in comparison with controls; an increase in the percentage of splenic megakaryocytes greater than 35 microns was also observed. A statistically significant increase in the total spleen content of CFU-Meg was observed after administration of 90,000 and 120,000 U rGM-CSF three times a day for 6 days, while no effect on bone marrow CFU-Meg was recorded, irrespective of the dose delivered. Finally, 24 hours after a single intravenous injection of rGM-CSF, there was a significant increase in the proportion of CFU-Meg in S-phase, with the splenic progenitors being more sensitive than bone marrow-derived CFU-Meg. These data indicate that rGM-CSF has in vivo megakaryocyte stimulatory activity, and are consistent with previous in vitro observations. However, an effective stimulation of megakaryocytopoiesis in vivo, bringing about an increase in the levels of blood platelets, may require interaction of rGM-CSF with other cytokines.
将小鼠重组粒细胞 - 巨噬细胞集落刺激因子(rGM - CSF)注射到小鼠体内,并评估其对骨髓、脾脏巨核细胞、巨核细胞前体(巨核细胞集落形成单位[CFU - Meg])的影响。在每天注射3次、连续6天注射12,000至120,000 U rGM - CSF的小鼠中,未观察到血小板水平和平均血小板体积有明显变化,而血液中性粒细胞增加了两倍。然而,通过测量75硒代蛋氨酸掺入血小板来评估的血小板生成率却相反,对于典型的“血小板生成素测定”,每天两次给予高达384,000 U rGM - CSF、持续2天,未能改变血小板生成。在接受60,000至120,000 U rGM - CSF的小鼠中,脾脏巨核细胞数量出现显著的剂量相关增加,而在注射120,000 U rGM - CSF的小鼠中,观察到骨髓巨核细胞数量略有增加。与对照组相比,接受rGM - CSF的小鼠中,大小小于18微米和大于35微米的骨髓巨核细胞比例显著更高;还观察到大于35微米的脾脏巨核细胞百分比增加。在每天3次、连续6天给予90,000和120,000 U rGM - CSF后,观察到脾脏CFU - Meg的总含量有统计学显著增加,而无论给予何种剂量,对骨髓CFU - Meg均无影响。最后,在单次静脉注射rGM - CSF 24小时后,S期CFU - Meg的比例显著增加,脾脏祖细胞比骨髓来源的CFU - Meg更敏感。这些数据表明rGM - CSF在体内具有巨核细胞刺激活性,与先前的体外观察结果一致。然而,在体内有效刺激巨核细胞生成并导致血小板水平升高,可能需要rGM - CSF与其他细胞因子相互作用。