Juneja H S, Minguell J J, Gardner F H, Helmer R E, Lee S
Prog Clin Biol Res. 1984;154:265-74.
To study the characteristics of the microenvironment of human bone marrow, fibroblasts derived from normal and aplastic anemia bone marrow aspirates or core biopsies were grown in culture. Normal bone marrow fibroblasts had a slow logarithmic phase of growth (8 days) with doubling times of 2 to 3 days. Aplastic anemia bone marrow fibroblasts had a rapid logarithmic phase of growth (5 to 6 days) and doubling times of 1 day. Dexamethasone (1 X 10(-8) M) stimulated the growth of normal fibroblasts. Growth of fibroblasts derived from aplastic anemia marrows was, however, inhibited by dexamethasone. Specific binding sites for the hormone were present in the normal fibroblasts (Bmax: 460-770 fmole/mg protein) whereas in the aplastic anemia fibroblasts the amount was very low (Bmax 27-215 fmole/mg protein). These observations suggest that in aplastic anemia, the bone marrow fibroblast, a cell constituent of the marrow microenvironment, has the capacity to develop and grow in vitro. However, this cell is different from normal bone marrow fibroblasts in its growth characteristics and response to dexamethasone.
为研究人类骨髓微环境的特征,将源自正常和再生障碍性贫血骨髓穿刺液或芯针活检的成纤维细胞进行体外培养。正常骨髓成纤维细胞生长的对数期缓慢(8天),倍增时间为2至3天。再生障碍性贫血骨髓成纤维细胞生长的对数期快速(5至6天),倍增时间为1天。地塞米松(1×10⁻⁸M)刺激正常成纤维细胞的生长。然而,地塞米松抑制再生障碍性贫血骨髓来源的成纤维细胞的生长。正常成纤维细胞中存在该激素的特异性结合位点(Bmax:460 - 770飞摩尔/毫克蛋白质),而再生障碍性贫血成纤维细胞中的含量非常低(Bmax 27 - 215飞摩尔/毫克蛋白质)。这些观察结果表明,在再生障碍性贫血中,骨髓成纤维细胞作为骨髓微环境的一种细胞成分,具有在体外发育和生长的能力。然而,这种细胞在生长特性和对地塞米松的反应方面与正常骨髓成纤维细胞不同。