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Effects of a phagocytosis-stimulating factor derived from polymorphonuclear neutrophils on the functions of macrophages.

机译:来源于多形核中性粒细胞的吞噬刺激因子对巨噬细胞功能的影响。

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摘要

The effects of phagocytosis-stimulating factor (PSF) derived from polymorphonuclear neutrophils on macrophage functions were studied. PSF enhanced the initial rate of phagocytosis of serum-opsonized zymosan particles by macrophages, whereas it did not affect the phagocytosis of immunoglobulin G-sensitized and inert zymosan particles. Kinetic studies showed that PSF accelerated the ingestion step, but not the attachment step, of phagocytosis by macrophages. On the other hand, PSF did not affect the other macrophage functions such as O2- generation, chemotaxis, adherence, and enzyme release. These results suggest that PSF may specifically modulate the complement receptor function of macrophages. Immunoblot assay showed the absence of components in macrophage which reacted with purified antibodies against polymorphonuclear neutrophil-derived PSF, and an extract from phagocytosing macrophages had no phagocytosis-stimulating activity, indicating that the macrophages did not produce PSF-like substances.
机译:研究了来自多形核中性粒细胞的吞噬刺激因子(PSF)对巨噬细胞功能的影响。 PSF增强了巨噬细胞吞噬血清调理的酵母聚糖颗粒的初始吞噬速率,而它不影响免疫球蛋白G敏化和惰性的酵母聚糖颗粒的吞噬作用。动力学研究表明,PSF加速了巨噬细胞吞噬作用的摄入步骤,但没有加快其附着步骤。另一方面,PSF不会影响其他巨噬细胞功能,例如O2的产生,趋化性,粘附和酶释放。这些结果表明,PSF可以特异性调节巨噬细胞的补体受体功能。免疫印迹分析显示巨噬细胞中没有与纯化的抗多形核中性粒细胞衍生的PSF抗体反应的成分,并且吞噬巨噬细胞的提取物没有刺激吞噬的活性,表明巨噬细胞未产生类似PSF的物质。

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