[Inducing effect of periodontopathic bacteria on activation of macrophage functions and production of interleukin-1 by mouse peritoneal macrophages].

K Honda, Y Ohmori
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Abstract

Periodontal disease is thought to be initiated by a bacterial infection and subsequently developed by immunopathological mechanisms thorough host-parasite interactions. The macrophage and lymphocyte are the major functional cell types in the lesion of the disease and participate in tissue destruction and alteration of the periodontal connective tissue as well as in host defense mechanisms. However, the detailed implications of macrophages in development of the disease is still unclear. The aim of this study was to gain more understanding of the functional role of macrophages in periodontal disease. In this study, we examined the inducing effects of sonicated extracts from some gram-negative and gram-positive bacteria associated with the pathogenesis of periodontal disease, including Bacteroides gingivalis, Fusobacterium nucleatum, Haemophilus actinomycetemcomitans, and Actinomyces viscosus, on activation of macrophage functions and IL-1 production by the macrophages from the mouse peritoneum. At a dose as low as 1 microgram/ml (dry weight) sonicated extracts from B. gingivalis induced an increase in acid phosphatase activity and in glucose consumption of mouse peritoneal macrophages in vitro. A significant increase in the acid phosphatase and in glucose consumption was observed in the cultures at 24 h and 48 h, respectively, after the addition of the sonicate. Sonicated extracts from A. viscosus, a gram-positive bacterium, as well as B. gingivalis, F. nucleatum, and H. actinomycetemcomitans, gram-negative ones, were able to induce the increase in acid phosphatase activity and in glucose consumption of the macrophages. These periodontopathic bacteria were found to strongly induce IL-1 production by the macrophages as early as 24 h after addition of the sonicates. A significant increase in the IL-1 production was observed at a dose of 1 microgram/ml of the sonicates. The inducing ability was equivalent to 1 microgram/ml Escherichia coli lipopolysaccharide. The highest production of IL-1 was observed in the macrophages treated with H. actinomycetemcomitans among these sonicates. Sonicated extracts from both gram-negative and gram-positive bacteria were able to induce the IL-1 production by macrophages from C3H/HeJ mice, which are LPS low-responders. These results suggest that periodontopathic bacteria have potent ability to induce macrophage activation and IL-1 production and that the activated macrophages may play an important role in development of periodontal disease.(ABSTRACT TRUNCATED AT 400 WORDS)

[牙周病菌对小鼠腹腔巨噬细胞激活巨噬细胞功能及产生白细胞介素-1的诱导作用]。
牙周病被认为是由细菌感染引起的,随后通过宿主-寄生虫相互作用的免疫病理机制发展而来。巨噬细胞和淋巴细胞是疾病病变的主要功能细胞类型,参与牙周结缔组织的组织破坏和改变以及宿主防御机制。然而,巨噬细胞在疾病发展中的具体意义尚不清楚。本研究旨在进一步了解巨噬细胞在牙周病中的功能作用。在这项研究中,我们检测了一些与牙周病发病相关的革兰氏阴性和革兰氏阳性细菌(包括牙龈拟杆菌、核梭杆菌、放线菌嗜血杆菌和粘胶放线菌)的超声提取物对小鼠腹膜巨噬细胞功能激活和IL-1产生的诱导作用。在低至1微克/毫升(干重)的剂量下,牙龈白杆菌超声提取物诱导体外小鼠腹膜巨噬细胞酸性磷酸酶活性和葡萄糖消耗增加。在24 h和48 h的培养中,分别观察到酸性磷酸酶和葡萄糖消耗的显著增加。革兰氏阳性菌黏杆菌、革兰氏阴性菌牙龈芽胞杆菌、核仁芽胞杆菌和放线菌comitans的超声提取物能够诱导巨噬细胞酸性磷酸酶活性和葡萄糖消耗的增加。研究发现,这些牙周病细菌早在添加超声后24小时就能强烈诱导巨噬细胞产生IL-1。在1微克/毫升的超声剂量下观察到IL-1产量的显著增加。诱导能力相当于1微克/毫升大肠杆菌脂多糖。其中放线菌孢子虫处理的巨噬细胞中IL-1的产量最高。革兰氏阴性菌和革兰氏阳性菌的超声提取物均能诱导LPS低反应的C3H/HeJ小鼠巨噬细胞产生IL-1。这些结果表明,牙周病细菌具有诱导巨噬细胞激活和IL-1产生的强大能力,激活的巨噬细胞可能在牙周病的发生中发挥重要作用。(摘要删节为400字)
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