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口腔微生物刺激下单核细胞中单核细胞趋化蛋白1和白细胞介素-8的产生

Monocyte chemoattractant protein 1 and interleukin-8 production in mononuclear cells stimulated by oral microorganisms.

作者信息

Jiang Y, Russell T R, Graves D T, Cheng H, Nong S H, Levitz S M

机构信息

The Evans Memorial Department of Clinical Research and the Department of Medicine, Boston University Medical Center Hospital and Boston City Hospital, Massachusetts 02118, USA.

出版信息

Infect Immun. 1996 Nov;64(11):4450-5. doi: 10.1128/iai.64.11.4450-4455.1996.

Abstract

Chemokines are a family of low-molecular-weight proinflammatory cytokines that stimulate recruitment of leukocytes. The chemokines interleukin-8 (IL-8) and monocyte chemoattractant protein 1 (MCP-1) are relatively specific chemoattractants for neutrophils and monocytes, respectively. Chemokine expression contributes to the presence of different leukocyte populations observed in normal and pathologic states. In the present studies, peripheral blood mononuclear cells (PBMC) were stimulated by microbes (Candida albicans, Streptococcus mutans, Porphyromonas gingivalis, and Actinobacillus actinomycetemcomitans) selected based upon their importance as oral pathogens. IL-8 and MCP-1 gene expression and protein release were determined by Northern blot (RNA blot) analysis and enzyme-linked immunosorbent assay. C. albicans, P. gingivalis, and A. actinomycetemcomitans induced high levels of production of both MCP-1 and IL-8. S. mutans was a strong inducer of MCP-1, but it did not stimulate significant production of IL-8. C. albicans, S. mutans, and A. actinomycetemcomitans were 500 to 5,000 times more potent than P. gingivalis in terms of MCP-1 production. In general, the microbe-to-PBMC ratios required for maximum gene expression of MCP-1 were lower than those for IL-8. However, for actual protein release of MCP-1 versus IL-8, differences in the effects of various microbe concentrations were observed only for A. actinomycetemcomitans. These results demonstrate that different oral pathogens induce specific dose-dependent patterns of chemokine gene expression and release. Such patterns may help explain the immunopathology of oral infections, particularly with regard to inflammatory leukocyte recruitment.

摘要

趋化因子是一类低分子量的促炎细胞因子,可刺激白细胞的募集。趋化因子白细胞介素 - 8(IL - 8)和单核细胞趋化蛋白1(MCP - 1)分别是中性粒细胞和单核细胞相对特异性的趋化因子。趋化因子的表达促成了在正常和病理状态下观察到的不同白细胞群体的存在。在本研究中,外周血单核细胞(PBMC)受到基于其作为口腔病原体的重要性而选择的微生物(白色念珠菌、变形链球菌、牙龈卟啉单胞菌和伴放线放线杆菌)的刺激。通过Northern印迹(RNA印迹)分析和酶联免疫吸附测定法测定IL - 8和MCP - 1基因表达及蛋白释放。白色念珠菌、牙龈卟啉单胞菌和伴放线放线杆菌诱导了高水平的MCP - 1和IL - 8产生。变形链球菌是MCP - 1的强诱导剂,但它不刺激IL - 8的显著产生。就MCP - 1产生而言,白色念珠菌、变形链球菌和伴放线放线杆菌的效力比牙龈卟啉单胞菌高500至5000倍。一般来说,MCP - 1最大基因表达所需的微生物与PBMC的比例低于IL - 8所需的比例。然而,对于MCP - 1与IL - 8的实际蛋白释放,仅在伴放线放线杆菌中观察到各种微生物浓度效应的差异。这些结果表明,不同的口腔病原体诱导趋化因子基因表达和释放的特定剂量依赖性模式。这种模式可能有助于解释口腔感染的免疫病理学,特别是关于炎症白细胞的募集。

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