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多形核白细胞迁移后Fc受体的出现及其在吞噬作用中的作用。

Appearance of Fc receptors on polymorphonuclear leukocytes after migration and their role in phagocytosis.

作者信息

Targowski S P, Niemialtowski M

出版信息

Infect Immun. 1986 Jun;52(3):798-802. doi: 10.1128/iai.52.3.798-802.1986.

Abstract

The effect of the migration of bovine blood polymorphonuclear leukocytes (PMNs) in vitro on their phagocytic activity was studied. PMNs were examined before and after migration through various membranes for rosette formation with sensitized sheep erythrocytes to detect Fc receptors (FcRs), phagocytic activity mediated through FcRs with opsonized staphylococci (Smith strain), and phagocytic activity mediated through nonimmunological receptors with unopsonized staphylococci (strain 305). Migration of PMNs was observed from the upper to the lower compartment of the blind well chamber through Millipore and Nuclepore membranes; through Millipore, Nuclepore, and nylon membranes coated with collagen; and through collagen-coated Millipore, Nuclepore, and nylon membranes overlaid with MA-104, BHK-21, MDBK-99, TB, or FBHE cells. Random migration of PMNs toward the plain medium (the same medium in the upper and lower compartments) through the membranes with and without a monolayer of cells increased the percentage of PMNs forming rosettes. In contrast, migration toward the medium containing lipopolysaccharide (LPS), formyl-L-methionyl-L-leucyl-L-phenylalanine (FMLP), or zymosan-activated serum (Act. serum) did not change the percentage of PMNs forming rosettes. The increased percentage of PMNs forming rosettes was associated with the enhanced phagocytosis of opsonized staphylococci (mediated by FcRs). In contrast, migration of PMNs toward LPS, FMLP, or Act. serum did not enhance phagocytosis mediated through FcRs. However, PMNs after migration toward LPS, FMLP, Act. serum, and plain medium enhanced phagocytosis of unopsonized staphylococci (mediated through the nonimmunological receptors).

摘要

研究了牛血液多形核白细胞(PMNs)体外迁移对其吞噬活性的影响。通过各种膜迁移前后的PMNs,用致敏绵羊红细胞检测Fc受体(FcRs)形成玫瑰花结的情况,通过FcRs介导的吞噬活性检测调理过的葡萄球菌(史密斯菌株),以及通过非免疫受体介导的吞噬活性检测未调理的葡萄球菌(305菌株)。观察到PMNs从盲孔室的上腔室通过微孔滤膜和核孔膜迁移到下腔室;通过涂有胶原蛋白的微孔滤膜、核孔膜和尼龙膜;以及通过覆盖有MA-104、BHK-21、MDBK-99、TB或FBHE细胞的胶原蛋白包被的微孔滤膜、核孔膜和尼龙膜。PMNs通过有无单层细胞的膜向普通培养基(上下腔室相同的培养基)随机迁移增加了形成玫瑰花结的PMNs百分比。相反,向含有脂多糖(LPS)、甲酰-L-蛋氨酰-L-亮氨酰-L-苯丙氨酸(FMLP)或酵母聚糖激活血清(活化血清)的培养基迁移并没有改变形成玫瑰花结的PMNs百分比。形成玫瑰花结的PMNs百分比增加与调理过的葡萄球菌(由FcRs介导)吞噬作用增强有关。相反,PMNs向LPS、FMLP或活化血清迁移并没有增强通过FcRs介导的吞噬作用。然而,向LPS、FMLP、活化血清和普通培养基迁移后的PMNs增强了未调理葡萄球菌的吞噬作用(通过非免疫受体介导)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5667/260929/75dabe1918e6/iai00105-0171-a.jpg

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