Fabian I, Lass M, Kletter Y, Golde D W
Department of Histology and Cell Biology, Sackler School of Medicine, Tel Aviv, Israel.
Blood. 1992 Aug 1;80(3):788-94.
We studied the effect of hematopoietic growth factors (granulocyte-macrophage colony-stimulating factor [GM-CSF], granulocyte [G]-CSF, interleukin (IL)-1, IL-3, IL-5, IL-6, and macrophage [M]-CSF) on differentiation and functional activity of human eosinophilic HL-60 cells (Eos-HL-60) and compared them with effects on parental HL-60 promyelocytic leukemia cells. Purified biosynthetic GM-CSF and IL-5 enhanced cell proliferation and induced eosinophilic differentiation in the eosinophilic subline in both liquid and agar cultures. IL-3 and IL-6 stimulated cell proliferation but had no effect on cell differentiation, whereas IL-1 and G-CSF affected neither differentiation nor proliferation of Eos-HL-60 cells under the conditions tested. GM-CSF-, IL-3-, and IL-5-treated Eos-HL-60 cells showed increased O2- production in response to phorbol esters (PMA), enhanced phagocytosis of Candida albicans, and release of the enzymes arylsulfatase, beta-glucuronidase and eosinophil peroxidase (EPO). The degranulation of eosinophils induced by GM-CSF, IL-5, and IL-3 may have relevance to the potential clinical toxicity of these hematopoietins, which also stimulate eosinophilopoiesis. G-CSF had no effect on enzyme release, oxidative metabolism, or phagocytic capacity of Eos-HL-60 cells. IL-5 did not affect proliferation, differentiation, or enzyme release in promyelocytic HL-60 cells. These results indicate the specificity of IL-5 for the eosinophil lineage, confirm the effects of GM-CSF and IL-3 on eosinophilopoiesis and mature eosinophil function in a model system, and indicate the absence of G-CSF and IL-1 stimulation of eosinophils. The Eos-HL-60 line is a useful model for studying human eosinophil responses to cytokines.
我们研究了造血生长因子(粒细胞 - 巨噬细胞集落刺激因子[GM - CSF]、粒细胞[G] - CSF、白细胞介素(IL)-1、IL - 3、IL - 5、IL - 6和巨噬细胞[M] - CSF)对人嗜酸性HL - 60细胞(Eos - HL - 60)分化和功能活性的影响,并将其与对亲代HL - 60早幼粒细胞白血病细胞的影响进行比较。纯化的生物合成GM - CSF和IL - 5在液体和琼脂培养中均增强了嗜酸性亚系中的细胞增殖并诱导了嗜酸性分化。IL - 3和IL - 6刺激细胞增殖,但对细胞分化无影响,而在测试条件下,IL - 1和G - CSF对Eos - HL - 60细胞的分化和增殖均无影响。经GM - CSF、IL - 3和IL - 5处理的Eos - HL - 60细胞对佛波酯(PMA)的反应显示O2 - 产生增加,白色念珠菌的吞噬作用增强,并且释放了芳基硫酸酯酶、β - 葡萄糖醛酸酶和嗜酸性粒细胞过氧化物酶(EPO)。GM - CSF、IL - 5和IL - 3诱导的嗜酸性粒细胞脱颗粒可能与这些造血素的潜在临床毒性有关,这些造血素也刺激嗜酸性粒细胞生成。G - CSF对Eos - HL - 60细胞的酶释放、氧化代谢或吞噬能力没有影响。IL - 5对早幼粒细胞HL - 60细胞的增殖、分化或酶释放没有影响。这些结果表明IL - 5对嗜酸性粒细胞谱系具有特异性,在模型系统中证实了GM - CSF和IL - 3对嗜酸性粒细胞生成和成熟嗜酸性粒细胞功能的影响,并表明不存在G - CSF和IL - 1对嗜酸性粒细胞的刺激。Eos - HL - 60系是研究人嗜酸性粒细胞对细胞因子反应的有用模型。