Warringa R A, Koenderman L, Kok P T, Kreukniet J, Bruijnzeel P L
Department of Pulmonary Diseases, University Hospital Utrecht, The Netherlands.
Blood. 1991 Jun 15;77(12):2694-700.
Eosinophilia and eosinophil function are regulated by cytokines such as granulocyte-macrophage colony-stimulating factor (GM-CSF), interleukin-3 (IL-3), and IL-5. We have investigated the modulatory role of GM-CSF and IL-3 on the platelet-activating factor (PAF)-, neutrophil-activating factor (NAF/IL-8)-, leukotriene B4 (LTB4)-, N-formyl-methionyl-leucyl-phenylalanine (FMLP)-, and human complement factor C5a-induced chemotaxis of eosinophils from normal individuals. These eosinophils show a chemotactic response toward PAF, LTB4, and C5a, but not to NAF/IL-8 and FMLP. Preincubation of the eosinophils with picomolar concentrations of GM-CSF caused a significant increase in the response toward LTB4 and induced a significant chemotactic response toward NAF/IL-8 and FMLP. Preincubation of the eosinophils with picomolar concentrations of IL-3 also induced a chemotactic response toward NAF/IL-8 and FMLP, and enhanced the PAF-induced chemotaxis response toward C5a was not influenced by both cytokines. Nanomolar concentrations of GM-CSF or IL-3 caused a significant inhibition of the C5a-induced chemotaxis. The LTB4-induced chemotaxis was also significantly inhibited in case of GM-CSF. At these concentrations both GM-CSF and IL-3 acted as chemotaxins for eosinophils were washed after pretreatment with GM-CSF and IL-3 the potentiation of the chemotactic response remained, whereas the inhibitory mode of action disappeared. Our data indicate that at picomolar concentrations the cytokines GM-CSF and IL-3 can modulate eosinophil chemotaxis and at nanomolar concentrations these cytokines can act as chemotaxins for eosinophils.
嗜酸性粒细胞增多和嗜酸性粒细胞功能受粒细胞-巨噬细胞集落刺激因子(GM-CSF)、白细胞介素-3(IL-3)和IL-5等细胞因子调节。我们研究了GM-CSF和IL-3对正常个体嗜酸性粒细胞的血小板活化因子(PAF)、中性粒细胞活化因子(NAF/IL-8)、白三烯B4(LTB4)、N-甲酰甲硫氨酰亮氨酰苯丙氨酸(FMLP)和人补体因子C5a诱导趋化作用的调节作用。这些嗜酸性粒细胞对PAF、LTB4和C5a表现出趋化反应,但对NAF/IL-8和FMLP无反应。用皮摩尔浓度的GM-CSF预孵育嗜酸性粒细胞,可显著增强对LTB4的反应,并诱导对NAF/IL-8和FMLP的显著趋化反应。用皮摩尔浓度的IL-3预孵育嗜酸性粒细胞,也可诱导对NAF/IL-8和FMLP的趋化反应,并增强PAF诱导的对C5a的趋化反应,且两种细胞因子对此均无影响。纳摩尔浓度的GM-CSF或IL-3可显著抑制C5a诱导的趋化作用。GM-CSF存在时,LTB4诱导的趋化作用也显著受到抑制。在这些浓度下,GM-CSF和IL-3均作为嗜酸性粒细胞的趋化因子,用GM-CSF和IL-3预处理后洗涤,趋化反应的增强作用仍然存在,而抑制作用模式消失。我们的数据表明,在皮摩尔浓度下,细胞因子GM-CSF和IL-3可调节嗜酸性粒细胞趋化作用,在纳摩尔浓度下,这些细胞因子可作为嗜酸性粒细胞的趋化因子。