Metcalf D
Walter and Eliza Hall Institute of Medical Research, Royal Melbourne Hospital, Victoria, Australia.
Proc Natl Acad Sci U S A. 1991 Dec 15;88(24):11310-4. doi: 10.1073/pnas.88.24.11310.
In clonal cultures of normal mouse marrow cells, combination of granulocyte, granulocyte-macrophage, or multipotential colony-stimulating factor (G-CSF, GM-CSF, or multi-CSF, respectively) with stem cell factor (SCF) did not alter the number of blast colonies stimulated to develop compared with SCF alone but induced an up to 25-fold increase in their mean cell content and an up to 6-fold increase in their mean progenitor cell content. Costimulation of blast colony formation by SCF plus G-CSF did not change the relative frequency of progenitor cells of different types within the colonies compared with colonies stimulated by SCF alone. However, combination of GM-CSF or multi-CSF with SCF significantly increased the relative frequency of granulocytic progenitors and, for multi-CSF, also of eosinophil progenitor cells. These changes in the relative frequencies of progenitor cells committed to the various lineages support the hypothesis that hemopoietic regulators have some ability to induce selective lineage commitment in the progeny of multipotential cells.
在正常小鼠骨髓细胞的克隆培养中,粒细胞集落刺激因子、粒细胞-巨噬细胞集落刺激因子或多能集落刺激因子(分别为G-CSF、GM-CSF或多能CSF)与干细胞因子(SCF)联合使用时,与单独使用SCF相比,刺激发育的原始集落数量没有改变,但平均细胞含量增加了25倍,平均祖细胞含量增加了6倍。与单独使用SCF刺激的集落相比,SCF加G-CSF共同刺激原始集落形成并没有改变集落内不同类型祖细胞的相对频率。然而,GM-CSF或多能CSF与SCF联合使用显著增加了粒细胞祖细胞的相对频率,对于多能CSF,还增加了嗜酸性粒细胞祖细胞的相对频率。这些定向分化为不同谱系的祖细胞相对频率的变化支持了造血调节因子具有某种能力诱导多能细胞后代选择性谱系定向分化这一假说。