Hanazawa S, Kawata Y, Takeshita A, Kumada H, Okithu M, Tanaka S, Yamamoto Y, Masuda T, Umemoto T, Kitano S
Department of Oral Microbiology, Meikai University School of Dentistry, Saitama, Japan.
Infect Immun. 1993 Dec;61(12):5219-24. doi: 10.1128/iai.61.12.5219-5224.1993.
The present study shows that monocyte chemotactic activity in crevicular fluids increases with severity of the disease and that a monocyte chemoattractant, monocyte chemoattractant protein 1 (MCP-1), is expressed as the predominant cytokine of gingival tissues and their fibroblasts treated with Porphyromonas (Bacteroides) gingivalis lipopolysaccharide (P-LPS). High monocyte chemotactic activity in the crevicular fluids was neutralized significantly by antiserum specific for the JE/MCP-1 protein. Marked expression of the MCP-1 gene was observed in the gingival tissues of all adult periodontal patients tested, but not in those of healthy subjects. Monocyte chemotactic activity was observed in culture supernatants of human normal gingival tissues treated with P-LPS, and the chemotactic activity increased in a dose-related manner. Expression of MCP-1 in P-LPS-treated human gingival fibroblasts was further examined. P-LPS induced the MCP-1 gene expression in a dose- and treatment time-dependent manner. The MCP-1 gene product in the culture supernatant was detected as two forms with molecular masses of 11,000 and 15,000 Da by immunoprecipitation with the specific antiserum. The MCP-1 gene expression was induced in the fibroblasts treated with interleukin-1 beta and tumor necrosis factor alpha, but not with interleukin-6. These results suggest that gingival fibroblasts can participate in monocyte recruitment in gingival tissues of adult periodontal patients via the MCP-1 gene product and that MCP-1 plays an important role in the inflammatory reaction in the disease.
本研究表明,龈沟液中的单核细胞趋化活性随疾病严重程度增加,且单核细胞趋化蛋白1(MCP-1)作为牙龈组织及其成纤维细胞经牙龈卟啉单胞菌(拟杆菌属)牙龈脂多糖(P-LPS)处理后的主要细胞因子表达。龈沟液中高单核细胞趋化活性被JE/MCP-1蛋白特异性抗血清显著中和。在所有受试成年牙周炎患者的牙龈组织中均观察到MCP-1基因的显著表达,而健康受试者中未观察到。在用P-LPS处理的人正常牙龈组织培养上清液中观察到单核细胞趋化活性,且趋化活性呈剂量相关增加。进一步检测了P-LPS处理的人牙龈成纤维细胞中MCP-1的表达。P-LPS以剂量和处理时间依赖性方式诱导MCP-1基因表达。通过用特异性抗血清进行免疫沉淀,在培养上清液中检测到MCP-1基因产物有两种形式,分子量分别为11,000和15,000 Da。用白细胞介素-1β和肿瘤坏死因子α处理成纤维细胞可诱导MCP-1基因表达,但用白细胞介素-6处理则不能。这些结果表明,牙龈成纤维细胞可通过MCP-1基因产物参与成年牙周炎患者牙龈组织中的单核细胞募集,且MCP-1在该疾病的炎症反应中起重要作用。