Dong F, Pouwels K, Hoefsloot L H, Rozemuller H, Löwenberg B, Touw I P
Department of Hematology, The Dr. Daniel den Hoed Cancer Center, Rotterdam, The Netherlands.
Exp Hematol. 1996 Feb;24(2):214-20.
Granulocyte colony-stimulating factor (G-CSF) promotes the survival and proliferation of myeloid progenitors and induces maturation of these cells toward terminally differentiated neutrophils. Using transfectants of the murine IL-3-dependent myeloid cell line 32D that express the human G-CSF receptor (32D/WT cells), we show here that G-CSF can also exert adverse effects on myeloid cell survival. Although initially enhancing IL-3-driven proliferation of 32D/WT cells, G-CSF strongly inhibited cell survival at later stages of culture. The loss of viability of 32D/WT cells following sustained G-CSF stimulation was not accompanied by progressive neutrophilic maturation. Instead, 32D/WT cells exhibited features characteristic of apoptosis. The apoptosis-inducing effect of G-CSF was seen at concentrations of IL-3 that could support long-term proliferation and survival of 32D/WT cells in the absence of G-CSF. Experiments with 32D cells expressing mutant forms of the G-CSF receptor revealed that the death signals were mediated exclusively through the membrane-distal cytoplasmic part of the G-CSF receptor, a region also involved in maturation signaling.
粒细胞集落刺激因子(G-CSF)可促进髓系祖细胞的存活和增殖,并诱导这些细胞成熟为终末分化的中性粒细胞。利用表达人G-CSF受体的小鼠IL-3依赖髓系细胞系32D的转染子(32D/WT细胞),我们在此表明G-CSF对髓系细胞存活也可产生不利影响。尽管G-CSF最初增强了32D/WT细胞的IL-3驱动增殖,但在培养后期它强烈抑制细胞存活。持续G-CSF刺激后32D/WT细胞活力丧失并未伴随渐进性嗜中性成熟。相反,32D/WT细胞表现出凋亡特征。在能够支持32D/WT细胞在无G-CSF情况下长期增殖和存活的IL-3浓度下,可观察到G-CSF的凋亡诱导作用。对表达G-CSF受体突变形式的32D细胞进行的实验表明,死亡信号仅通过G-CSF受体的膜远端胞质部分介导,该区域也参与成熟信号传导。