首页> 外文期刊>Journal of Endodontics: Official Journal of American Association of Endodontists >Production of macrophage inflammatory protein (MIP)-1alpha and MIP-1beta by human polymorphonuclear neutrophils stimulated with Porphyromonas endodontalis lipopolysaccharide.
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Production of macrophage inflammatory protein (MIP)-1alpha and MIP-1beta by human polymorphonuclear neutrophils stimulated with Porphyromonas endodontalis lipopolysaccharide.

机译:牙本质卟啉菌脂多糖刺激人多形核中性粒细胞产生巨噬细胞炎性蛋白(MIP)-1alpha和MIP-1beta。

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摘要

This study was undertaken to investigate the capacity of polymorphonuclear neutrophils (PMNs) to secrete Macrophage Inflammatory Protein (MIP)-1alpha and MIP-1beta after stimulation with Porphyromonas endodontalis lipopolysaccharide (LPS). Escherichia coli LPS was used as a positive control. Venous blood was collected and PMNs were isolated from healthy volunteers. Cells were cultured with various concentrations of LPS for different periods of time. Cell supernatants were assayed by enzyme-linked immunosorbent assay. The levels of chemokine secretion in PMNs stimulated with each LPS were found to be significantly higher than in the unstimulated control cells (p < 0.05), and this expression occurred in a time- and dose-dependent manner. E. coli LPS induced higher levels of cytokines than P. endodontalis LPS. These findings demonstrated that P. endodontalis LPS is capable of stimulating PMNs to produce chemotactic cytokines and suggested that PMNs stimulated with P. endodontalis LPS may play a crucial role in the inflammatory and immunopathological reactions of pulpal and periapical diseases.
机译:进行这项研究以研究用牙髓卟啉单胞菌脂多糖(LPS)刺激后多形核中性粒细胞(PMN)分泌巨噬细胞炎性蛋白(MIP)-1alpha和MIP-1beta的能力。大肠杆菌LPS用作阳性对照。收集静脉血,并从健康志愿者中分离出PMN。用不同浓度的LPS将细胞培养不同的时间。通过酶联免疫吸附测定法测定细胞上清液。发现每个LPS刺激的PMN中趋化因子分泌水平显着高于未刺激的对照细胞(p <0.05),并且该表达以时间和剂量依赖性方式发生。大肠杆菌LPS诱导的细胞因子水平高于牙髓假单胞菌LPS。这些发现表明,牙髓假单胞菌LPS能够刺激PMNs产生趋化性细胞因子,并表明用牙髓假单胞菌LPS刺激的PMNs可能在牙髓和根尖周炎的炎症和免疫病理反应中起关键作用。

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