Boll I T
Acta Haematol. 1981;66(3):187-94. doi: 10.1159/000207118.
Continuous observation of living cells by phase-contrast time lapse microcinematography revealed different origins of multinuclear cells and cells with lobed nuclei in the hematopoietic progenitor cell series, which must be classified as megakaryoblasts, the determined progenitor cells of the megakaryopoietic series. Hematopoietic progenitor cells with single nuclei of nuclear diameter 5-13 microns, the promegakaryoblasts, may become polyploid by various means: by postmitotic cytoplasmic fusion, by consecutive nuclear fusion, by endomitosis, or by nuclear amitosis or lobe formation presumably after endoreduplication and nuclear growth. Including amitotic nuclear division in the mitotic rate of normal progenitor cells nearly the half of all these cells in G2 phase (0.4) produce in vitro octoploid megakaryoblasts, respectively osteoclasts. Thrombopoietin-rich sera in the medium enhance the mitotic index of the hematopoietic progenitor cell line from 0.1 to 0.25, but do not change the proportion of polyploid mitoses.
通过相差延时显微电影摄影术对活细胞进行连续观察发现,造血祖细胞系列中多核细胞和核呈叶状的细胞有不同起源,这些细胞必须归类为巨核母细胞,即巨核细胞生成系列中已确定的祖细胞。核直径为5 - 13微米的单核造血祖细胞,即早巨核母细胞,可通过多种方式变成多倍体:通过有丝分裂后细胞质融合、连续核融合、核内有丝分裂,或可能在核内复制和核生长后通过核无丝分裂或核叶形成。将核无丝分裂计入正常祖细胞的有丝分裂率,在G2期几乎一半的这些细胞(0.4)分别在体外产生八倍体巨核母细胞或破骨细胞。培养基中富含血小板生成素的血清可将造血祖细胞系的有丝分裂指数从0.1提高到0.25,但不会改变多倍体有丝分裂的比例。