Tsuda T, Wong D, Dolovich J, Bienenstock J, Marshall J, Denburg J A
Department of Medicine, McMaster University, Hamilton, Ontario, Canada.
Blood. 1991 Mar 1;77(5):971-9.
We have recently shown that nerve growth factor (NGF) promotes human granulopoiesis, specifically augmenting basophilic cell differentiation observed in methylcellulose hematopoietic colony assays of human peripheral blood. Because the NGF effect was seen in the presence of conditioned medium derived from a human T-cell line (Mo-CM) containing granulocyte-macrophage colony-stimulating factor (GM-CSF), we examined interactions of purified NGF and recombinant human GM-CSF (rhGM-CSF) on granulocyte growth and differentiation. rhGM-CSF stimulated a dose-dependent increase in methylcellulose colony growth at concentrations between 0.1 U/mL and 10 U/mL, and in the presence of NGF at 500 ng/mL this effect was enhanced. The number of basophilic cell colony-forming units (CFU-Baso) and histamine-positive colonies increased synergistically when NGF was added to rhGM-CSF. Furthermore, because Mo-CM acts with sodium butyrate to promote basophilic differentiation of alkaline-passaged myeloid leukemia cells, HL-60, we also examined the interaction of NGF and Mo-CM or rhGM-CSF using this assay. In the presence of NGF, Mo-CM at concentrations of 0.5% to 20% vol/vol, and rhGM-CSF at concentrations of 0.1 U/mL to 100 U/mL synergistically increased histamine production by butyrate-induced, alkaline-passaged HL-60 cells; this was associated with the appearance of metachromatic, tryptase-negative, IgE receptor-positive cells. The effects of rhGM-CSF or Mo-CM were completely abrogated by a specific anti-rhGM-CSF neutralizing antibody in methylcellulose, with or without NGF; the NGF synergy with rhGM-CSF in the HL-60 assay was also inhibited by either anti-rhGM-CSF or anti-NGF antibody. These studies support the notion that differentiation in the basophilic lineage may be enhanced by NGF acting to increase the number of GM-CSF-responsive basophilic cell progenitors.
我们最近发现,神经生长因子(NGF)可促进人类粒细胞生成,特别是在人类外周血甲基纤维素造血集落试验中增强嗜碱性细胞分化。由于在含有粒细胞 - 巨噬细胞集落刺激因子(GM - CSF)的人T细胞系条件培养基(Mo - CM)存在的情况下观察到了NGF效应,我们研究了纯化的NGF与重组人GM - CSF(rhGM - CSF)对粒细胞生长和分化的相互作用。rhGM - CSF在0.1 U/mL至10 U/mL的浓度范围内刺激甲基纤维素集落生长呈剂量依赖性增加,并且在存在500 ng/mL NGF的情况下,这种效应会增强。当将NGF添加到rhGM - CSF中时,嗜碱性细胞集落形成单位(CFU - Baso)和组胺阳性集落的数量协同增加。此外,由于Mo - CM与丁酸钠共同作用可促进碱性传代的髓系白血病细胞HL - 60的嗜碱性分化,我们还使用该试验研究了NGF与Mo - CM或rhGM - CSF的相互作用。在存在NGF的情况下,0.5%至20%体积/体积浓度的Mo - CM以及0.1 U/mL至100 U/mL浓度的rhGM - CSF可协同增加丁酸钠诱导的碱性传代HL - 60细胞的组胺产生;这与异染性、类胰蛋白酶阴性、IgE受体阳性细胞的出现有关。在甲基纤维素中,无论有无NGF,rhGM - CSF或Mo - CM的效应均被特异性抗rhGM - CSF中和抗体完全消除;在HL - 60试验中,NGF与rhGM - CSF的协同作用也被抗rhGM - CSF或抗NGF抗体抑制。这些研究支持这样一种观点,即嗜碱性谱系的分化可能通过NGF增加对GM - CSF反应性嗜碱性细胞祖细胞的数量而得到增强。