Kawakita M, Yamamoto S, Asou N, Ishii M, Sakaguchi M, Takatsuki K
Br J Haematol. 1986 Apr;62(4):715-22. doi: 10.1111/j.1365-2141.1986.tb04095.x.
The level of urinary Meg-CSF activity in patients with various thrombopoietic disorders was studied. Five out of eight patients with idiopathic thrombocytopenic purpura had megakaryocytic hyperplasia in the marrow and increased Meg-CSF activity in the urine. Urinary Meg-CSF activity in patients with polycythaemia vera and essential thrombocythaemia was normal. There was a significant inverse correlation between urinary Meg-CSF activity and peripheral blood platelet count but not bone marrow megakaryocyte mass. There was a significant increase of urinary Meg-CSF activity during the period of thrombocytopenia after chemotherapy in patients with acute leukaemia who were in complete remission. The timing of maximal Meg-CSF levels corresponded to the nadirs of platelet counts. These results support the concept that Meg-CSF may play a significant role in the regulation of megakaryopoiesis and/or thrombopoiesis in vivo.
对患有各种血小板生成障碍的患者的尿巨核细胞集落刺激因子(Meg-CSF)活性水平进行了研究。8例特发性血小板减少性紫癜患者中有5例骨髓中巨核细胞增生,尿中Meg-CSF活性增加。真性红细胞增多症和原发性血小板增多症患者的尿Meg-CSF活性正常。尿Meg-CSF活性与外周血血小板计数之间存在显著的负相关,但与骨髓巨核细胞数量无关。急性白血病完全缓解患者化疗后血小板减少期间,尿Meg-CSF活性显著增加。Meg-CSF水平最高的时间与血小板计数的最低点相对应。这些结果支持了Meg-CSF可能在体内巨核细胞生成和/或血小板生成的调节中起重要作用这一概念。