Hibbin J A, Njoku O S, Matutes E, Lewis S M, Goldman J M
Br J Haematol. 1984 Jul;57(3):495-503. doi: 10.1111/j.1365-2141.1984.tb02924.x.
We have measured the numbers of myeloid progenitor cells in the circulation of patients with myelofibrosis (MF) and other myeloproliferative disorders. In general, progenitor cell numbers were increased in the circulation of patients with MF compared with controls. The mean increases were 9-fold for the multilineage progenitor cells (CFU-GEMM), 13-fold for the erythroid progenitor cells (BFU-E), 37-fold for the granulocyte-macrophage progenitor cells (CFU-GM) and 167-fold for the megakaryocyte progenitors (CFU-MK). Splenectomized patients generally had reduced numbers of circulating progenitor cells. In the CFU-MK assay, mature megakaryocytes cultured from patients with MF regularly showed large vacuoles in the nucleus and cytoplasm, unlike control cells. The increased colony formation in patients with MK, involving especially CFU-MK colonies, is consistent with the hypothesis that MF is a primary myeloproliferative disorder in which a megakaryocyte-derived factor predisposes to the formation of marrow fibrosis.
我们已经测量了骨髓纤维化(MF)患者及其他骨髓增殖性疾病患者循环系统中的髓系祖细胞数量。总体而言,与对照组相比,MF患者循环系统中的祖细胞数量增加。多系祖细胞(CFU-GEMM)平均增加9倍,红系祖细胞(BFU-E)增加13倍,粒-巨噬系祖细胞(CFU-GM)增加37倍,巨核系祖细胞(CFU-MK)增加167倍。脾切除患者循环祖细胞数量通常减少。在CFU-MK检测中,与对照细胞不同,MF患者培养出的成熟巨核细胞在细胞核和细胞质中常有大空泡。MK患者中集落形成增加,尤其是CFU-MK集落,这与MF是一种原发性骨髓增殖性疾病的假说一致,在该疾病中,一种源自巨核细胞的因子易导致骨髓纤维化形成。