Kido J, Kido R, Kataoka M, Fagerhol M K, Nagata T
Department of Periodontology and Endodontology, Tokushima University School of Dentistry, Tokushima, Japan.
Oral Microbiol Immunol. 2004 Jun;19(3):182-7. doi: 10.1111/j.0902-0055.2004.00139.x.
Calprotectin, a major cytosolic protein of leukocytes, is detected in neutrophils, monocytes/macrophages, and epithelial cells. This protein is known to be a marker for several inflammatory diseases and is detected in inflammatory gingival tissue with periodontal disease. Recently, we found that the calprotectin level in gingival crevicular fluid from periodontitis patients was significantly higher than that of healthy subjects. However, the regulation of calprotectin in periodontal disease is unclear. In the present study, we investigated the effect of lipopolysaccharides of periodontopathic bacteria on calprotectin release from human neutrophils. Neutrophils from healthy donors were treated with lipopolysaccharides from Porphyromonas gingivalis (P-LPS), Actinobacillus actinomycetemcomitans, Prevotella intermedia, Fusobacterium nucleatum, and Escherichia coli. Calprotectin of neutrophil was identified by immunoblotting and calprotectin amount was determined by ELISA. Two subunits (10 and 14 kDa) of calprotectin were observed in the cell and medium fractions from neutrophils. P-LPS increased calprotectin release from seven to 16 times the control level after 30 min and its effect appeared in a dose-dependent manner (10-1000 ng/ml). Lipopolysaccharides from A. actinomycetemcomitans, P. intermedia, F. nucleatum, and E. coli also induced calprotectin release from neutrophils. These results suggest that lipopolysaccharides from periodontopathic bacteria induce calprotectin release from human neutrophils.
钙卫蛋白是白细胞的一种主要胞质蛋白,可在中性粒细胞、单核细胞/巨噬细胞及上皮细胞中检测到。已知该蛋白是多种炎症性疾病的标志物,在患有牙周病的炎症性牙龈组织中也可检测到。最近,我们发现牙周炎患者龈沟液中的钙卫蛋白水平显著高于健康受试者。然而,牙周病中钙卫蛋白的调节机制尚不清楚。在本研究中,我们调查了牙周病原菌的脂多糖对人中性粒细胞释放钙卫蛋白的影响。用牙龈卟啉单胞菌(P-LPS)、伴放线放线杆菌、中间普氏菌、具核梭杆菌和大肠杆菌的脂多糖处理健康供体的中性粒细胞。通过免疫印迹鉴定中性粒细胞的钙卫蛋白,并用酶联免疫吸附测定法测定钙卫蛋白的含量。在中性粒细胞的细胞和培养基组分中观察到钙卫蛋白的两个亚基(10 kDa和14 kDa)。30分钟后,P-LPS使钙卫蛋白的释放量增加至对照水平的7到16倍,且其作用呈剂量依赖性(10 - 1000 ng/ml)。伴放线放线杆菌、中间普氏菌、具核梭杆菌和大肠杆菌的脂多糖也诱导中性粒细胞释放钙卫蛋白。这些结果表明,牙周病原菌的脂多糖可诱导人中性粒细胞释放钙卫蛋白。