Ogawa M, Porter P N, Terasawa T, Brockbank K G
Exp Hematol. 1980;8 Suppl 8:90-102.
We have discovered that human and rabbit bone marrow conditioned media (BMCM) promote the growth of bursts in cultures containing erythropoietin. We then demonstrated that the measurement of 59Fe incorporation into heme was a more quantitative assay for burst-promoting activity (BPA) than counting burst numbers. Furthermore, we have observed that the use of low (less than 15%) concentrations of fetal calf serum is a convenient way of reducing endogenous sources of BPA for studies of the BPA in the test samples. When 59Fe incorporation and cell numbers of individual rabbit erythropoietic bursts were analyzed simultaneously, BPA caused a shift in the cumulative frequency distributions without changes in their shapes. These results indicated that BPA augments hemoglobin synthesis by stimulating cell proliferation during the early phase of burst formation. In addition, human BPA increased the relative proportion of fetal hemoglobin in the hemoglobins synthesized by adult circulating BFU-e. BPA appears to augment cell proliferation of early precursors which are committed to produce F cells.
我们发现,在含有促红细胞生成素的培养物中,人及兔骨髓条件培养基(BMCM)可促进爆式集落的生长。然后我们证明,测定59Fe掺入血红素的量比计数爆式集落数量是一种更定量的爆式集落促进活性(BPA)检测方法。此外,我们观察到,使用低浓度(低于15%)的胎牛血清是减少测试样品中BPA内源性来源的一种便捷方法,便于研究BPA。当同时分析单个兔红细胞生成爆式集落的59Fe掺入量和细胞数量时,BPA导致累积频率分布发生偏移,但其形状不变。这些结果表明,BPA在爆式集落形成的早期阶段通过刺激细胞增殖来增强血红蛋白合成。此外,人BPA增加了成年循环BFU-e合成的血红蛋白中胎儿血红蛋白的相对比例。BPA似乎增强了致力于产生F细胞的早期前体细胞的增殖。