Lundahl J, Dahlgren C, Gustavsson K, Hed J
Dept. of Clinical Immunology and Transfusionmedicine, Karolinska Hospital, Stockholm, Sweden.
Inflamm Res. 1995 Oct;44(10):438-46. doi: 10.1007/BF01757701.
We have investigated the effect of gradual degranulation on the expression of functional receptors (CR1 and CR3) on human neutrophils. Incubation with increasing concentrations of fMLP (10(-10) - 10(-7) M) translocated CR1 and CR3 to the cell surface in a similar kinetic pattern. When reaching maximal expression of receptors (10(-7) M fMLP), 78 +/- 10% and 87 +/- 9% of the total pool of CR1 and CR3, respectively, were translocated to the cell surface. To drive the mobilization process further, cytochalasin B was introduced to increase the stimulatory effect of fMLP. No further increase in CR1 surface expression was obtained. However, we found a characteristic time course of surface appearance of CR1 and CR3 with a maximal surface expression within 1 minute, followed by a time-related down-regulation of CR1 but not CR3. In addition, the total pool of CR1 in cytochalasin B treated neutrophils was reduced after 15 minutes stimulation with fMLP measured by flow cytometry and immunoblotting, indicating degradation of CR1. The down-regulation of CR1 was concomitant with a translocation of azurophil granules, in terms of upregulation of CD63. Azurophil, but not specific nor secretory, granule fractions caused a down-regulation of CR1 on fMLP activated neutrophils. The presence of human sera and serine protease inhibitor protected CR1 from down-regulation. Together, these findings indicate that intracellular stored proteases, released in the late part of the sequential mobilization process, alters the expression of functional receptors mobilized in the early part of the mobilization process. The findings also focus on the importance of the microenvironment for the net outcome of neutrophil activation in terms of functional receptor expression.
我们研究了逐步脱颗粒对人中性粒细胞上功能性受体(CR1和CR3)表达的影响。用浓度递增的fMLP(10⁻¹⁰ - 10⁻⁷ M)孵育,可使CR1和CR3以相似的动力学模式转位至细胞表面。当达到受体的最大表达量(10⁻⁷ M fMLP)时,CR1和CR3总量中分别有78±10%和87±9%转位至细胞表面。为进一步推动动员过程,引入细胞松弛素B以增强fMLP的刺激作用。CR1的表面表达未进一步增加。然而,我们发现CR1和CR3的表面出现具有特征性的时间进程,在1分钟内达到最大表面表达,随后CR1出现与时间相关的下调,而CR3未下调。此外,通过流式细胞术和免疫印迹法检测,在用fMLP刺激15分钟后,经细胞松弛素B处理的中性粒细胞中CR1的总量减少,表明CR1发生了降解。CR1的下调与嗜天青颗粒的转位同时发生,表现为CD63上调。嗜天青颗粒组分而非特异性或分泌性颗粒组分导致fMLP激活的中性粒细胞上CR1下调。人血清和丝氨酸蛋白酶抑制剂的存在可保护CR1不发生下调。总之,这些发现表明,在相继动员过程后期释放的细胞内储存蛋白酶,会改变在动员过程早期动员的功能性受体的表达。这些发现还强调了微环境对于中性粒细胞激活在功能性受体表达方面的最终结果的重要性。