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Influence of macrophage activation on their capacity to bind bacterial antigens studied with atomic force microscopy

机译:巨噬细胞活化对其结合细菌抗原能力的影响用原子力显微镜研究

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In this work we studied interactions between bacterial antigens and receptors on the surface of macrophages using atomic force microscopy (AFM).We used two bacterial cell wall components: lipopolysaccharide (LPS) derived from gram-negative Escherichia coli and exopolysaccharide (EPS) derived from gram-positive Lactobacillus rhamnosus.Interactions between these bacterial antigens and immune cell receptors were studied in peritoneal macrophages derived from two strains of mice, CBA and C3H/J,in which the Toll-like receptor 4 (TLR4) is genetically disabled.We collected 500 force-distance curves for LPS-activated cells using an EPS-covered AFM tip,and for EPS- activated cells using an LPS-covered AFM tip.Nonactivated cells were tested as reference cells.The results show that LPS-primed macrophages decrease their ability to bind EPS.Surprisingly,EPS- activated macrophages maintain or even increase their ability to bind LPS.This may suggest that in vivo commensal enteric bacteria,such as lactobacilli,will enhance the defense potential of local macrophages against pathogens expressing LPS.
机译:在这项工作中,我们使用原子力显微镜(AFM)研究了细菌抗原与巨噬细胞表面受体之间的相互作用。我们使用了两种细菌细胞壁成分:革兰氏阴性大肠杆菌衍生的脂多糖(LPS)和衍生自革兰氏阴性大肠杆菌的胞外多糖(EPS)在来自CBA和C3H / J两种小鼠的腹膜巨噬细胞中研究了这些细菌抗原与免疫细胞受体之间的相互作用,其中Toll样受体4(TLR4)被基因禁用。使用EPS覆盖的AFM尖端的LPS激活的细胞和使用LPS覆盖的AFM尖端的EPS激活的细胞的500力-距离曲线。未激活的细胞作为参考细胞进行测试。结果表明,LPS激活的巨噬细胞减少了它们的作用力令人惊讶的是,EPS活化的巨噬细胞维持甚至增加了其结合LPS的能力。这可能表明体内共生肠细菌,例如紫胶烟草,将增强局部巨噬细胞对表达LPS的病原体的防御能力。

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