Fukada Y
Department of Medicine II, Hokkaido University School of Medicine, Sapporo, Japan.
Hokkaido Igaku Zasshi. 1998 Nov;73(6):543-56.
We have developed a system of erythroid-lineage-specific expansion of purified human peripheral blood (PB) CD34 positive cells mobilized by a granulocyte-colony stimulating factor (G-CSF), as an in vitro model for the study of the process of proliferation and differentiation of erythroid progenitor cells. In this system, PB CD34 positive cells terminally differentiated into reticulocytes, which made it feasible to conduct a study on enucleation process of human erythroblasts. Erythroid differentiation/maturation was induced in the highly purified PB CD34 positive cells in the liquid suspension culture with interleukin-3 (IL-3), stem cell factor (SCF; a ligand for c-kit) and human erythropoietin (EP); 8 days of the culture generated progenitors equivalent to colony-forming units-erythroid (CFU-E) and 12 days of the culture generated a population mainly consisting of polychromatophilic normoblasts. Within additional 4 days of the suspension culture, these cells contained hemoglobin, differentiated to orthochromatic normoblasts, and became capable of enucleation in vitro, in a time-dependent manner. Removal of all serum from the culture medium, with or without cytokines, including IL-3, SCF and EP, did not affect enucleation processes of the cells on 12th day. On electron microscopy, the incipient reticulocytes contained all cellular organelles except the nucleus, and the extruding nucleus was surrounded by a plasma membrane. Colchicine and vinblastine blocked nuclear multiplication and cytochalasin D blocked cell division with formation of multinucleated cells. Only cytochalasin D completely inhibited enucleation, which was recovered by washing out the cytochalasin D in the 12th day cell cultures. Thus, human erythroblasts do not require cytokines, including EP in their enucleation process. In this process, the contraction of filamentous actin occurs, while microtubules apparently do not participate.
我们开发了一种系统,可对由粒细胞集落刺激因子(G-CSF)动员的纯化人外周血(PB)CD34阳性细胞进行红系特异性扩增,作为研究红系祖细胞增殖和分化过程的体外模型。在该系统中,PB CD34阳性细胞终末分化为网织红细胞,这使得对人成红细胞去核过程的研究成为可能。在含有白细胞介素-3(IL-3)、干细胞因子(SCF;c-kit的配体)和人促红细胞生成素(EP)的液体悬浮培养中,高度纯化的PB CD34阳性细胞被诱导发生红系分化/成熟;培养8天产生相当于红系集落形成单位(CFU-E)的祖细胞,培养12天产生主要由嗜多色性正成红细胞组成的细胞群体。在悬浮培养额外的4天内,这些细胞含有血红蛋白,分化为正染性正成红细胞,并能够在体外以时间依赖性方式去核。从培养基中去除所有血清,无论有无细胞因子,包括IL-3、SCF和EP,均不影响第12天细胞的去核过程。电子显微镜观察显示,初期的网织红细胞除细胞核外含有所有细胞器,挤出的细胞核被质膜包围。秋水仙碱和长春碱阻断核增殖,细胞松弛素D阻断细胞分裂并形成多核细胞。只有细胞松弛素D完全抑制去核,在第12天的细胞培养物中洗去细胞松弛素D后去核可恢复。因此,人成红细胞在去核过程中不需要细胞因子,包括EP。在这个过程中,丝状肌动蛋白发生收缩,而微管显然不参与。