Dallegri F, Patrone F, Frumento G, Ballestrero A, Sacchetti C
Exp Hematol. 1985 Mar;13(3):209-14.
This study investigated the influence of a chemotactic stimulus on the extracellular cytotoxicity mediated by phagocytosing polymorphonuclear neutrophilic leukocytes (PMN). We used N-formyl-methionyl-leucyl-phenylalanine (FMLP) as chemotactic peptide, opsonized zymosan as phagocytosable particle, and ox red blood cells (ORBC) as extracellular bystander targets. Phagocytosing PMN were found to kill ORBC efficiently, as determined by the 51Cr-release assay. FMLP, at the concentration of 100 nM, significantly enhanced the target cell lysis. PMN from two patients with chronic granulomatous disease and normal PMN plus catalase or free radical scavengers (mannitol, benzoate, histidine) were completely devoid of cytolytic activity both in the presence and in the absence of FMLP. The results indicate that the target cell lysis by phagocytosing PMN as well as the chemotactic peptide-related amplification of the lysis itself depend on the expression of the PMN oxidative cytotoxic potential. A similar response to a chemotactic stimulus in vivo could provide a mechanism for regulating PMN-dependent cytotoxic and inflammatory processes.
本研究调查了趋化刺激对吞噬多形核嗜中性白细胞(PMN)介导的细胞外细胞毒性的影响。我们使用N-甲酰甲硫氨酰-亮氨酰-苯丙氨酸(FMLP)作为趋化肽,调理酵母聚糖作为可吞噬颗粒,氧化型红细胞(ORBC)作为细胞外旁观者靶标。通过51Cr释放试验测定,发现吞噬PMN能有效地杀死ORBC。100 nM浓度的FMLP显著增强了靶细胞裂解。两名慢性肉芽肿病患者的PMN以及正常PMN加过氧化氢酶或自由基清除剂(甘露醇、苯甲酸盐、组氨酸)在有和没有FMLP的情况下均完全没有细胞溶解活性。结果表明,吞噬PMN引起的靶细胞裂解以及裂解本身的趋化肽相关放大取决于PMN氧化细胞毒性潜能的表达。体内对趋化刺激的类似反应可能为调节PMN依赖性细胞毒性和炎症过程提供一种机制。