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Cell adhesion molecules and cytokines in periodontal disease

Cell adhesion molecules and cytokines in periodontal disease
牙周病中的细胞粘附分子和细胞因子
批准号:
10307054
负责人:
TANAKA Akio
金额:
$22.85万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (A).
财政年份:
1998
资助国家:
日本
项目状态:
已结题
起止时间:
1998 至 2000

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中文摘要
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英文摘要
We studied the role of cell adhesion molecules and cytokines in periodontal diseases, and obtained the following results. The primary difference in the characterization of both cells and matrix was in the adhesion between fibroblasts and extracellular matrix. Both CD43 and a glycoprotein of about 45-kDa played roles in the adhesion sequence between fibroblasts and immunocompetent cells. Fibroblasts derived from hyperplastic gingiva produced abundant quantities of both TGF-β and IL-6 when stimulated by LPS.In rat experimental periodontitis, leukocyte chemotactic factor was produced not only by inflammatory cells but also by junctional epithelial cells. There was a direct correlation between the amount of hepatocyte growth factor in gingival crevicular fluid and other parameters of periodontal disease such as probing depth, gingival index and amount of IL-1β. Among the several PGE2 receptors expressed on fibroblasts, EP2 and EP4 receptors were identified as those involved with the inhibi … More tion of ICAM-1 expression. Stimulation by HSP60 of mononuclear cells from peripheral blood of patients with advanced periodontitis produced significantly increased expression of IFN-γ at both the mRNA and protein levels. The ratio of IFN-γ derived from mononuclear cells within periodontally involved gingival tissues to that of mononuclear cells from peripheral blood of the same patients was lower, whereas the respective ratio for IL -4 was higher. There was interruption of apoptosis within lymp hocytes from gingiva involved with periodontitis due to diminished signal transfer as well as molecular apoptosis inhibition. Peritoneal re-infection of rats immunized to A.actinomycetemcomitans resulted in increased production of both TNF-α and IL-6, thus leading to markedly increased production of IFN-γ. Five serotypes, a through e, of A.actinomycetemcomi tans were genetically identified. PCR techniques and base sequence analysis have led to methods of serotype identification that are very useful in understanding the pathogenesis and diagnosis of periodontal disease. Less
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Suzuki N et al.: "Genetic analysis of the gene cluster for the synthesis of serotype a-specific polysaccharide antigen in Actinobacillus actinomycetemcomitans"Biochim Biophys Acta. 1517巻・1号. 135-138 (2000)
Suzuki N 等人:“Actinobacillus actinomycetemcomitans 中合成血清型 a 特异性多糖抗原的基因簇”Biochim Biophys Acta,第 1517 卷,第 135-138 期(2000 年)。
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Y Nakano,N Suzuki,Y Yoshida,T Nezu,Y Yamashita,T Koga: "Thymidine diphosphate-6-deoxy-L-lyxo-4-hexulose reductase synthesizing dTDP-6-deoxy-L-talose from Actinobacillus actinomycetem-"J Biol Chem. 275(10). 6806-6812 (2000)
Y Nakano,N Suzuki,Y Yoshida,T Nezu,Y Yamashita,T Koga:“胸苷二磷酸-6-脱氧-L-lyxo-4-己酮糖还原酶从放线杆菌中合成 dTDP-6-脱氧-L-塔罗糖-”J
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Noguchi K: "Involvement of cyclooxygenase-2 in interleukin-lalpha-induced prostaglandin production by human periodontal ligament cells" J Periodontol. (掲載予定). (1999)
Noguchi K:“环氧合酶-2 参与白细胞介素-lα 诱导的人牙周膜细胞产生前列腺素”J periodontol(即将出版)。
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Yoshida A et al.: "Immunodominant region of Actinobacillus actinomycetemcomitans 40-kilodalton heat shock protein in patients with rheumatoid arthritis"J Dent Res. 80 (1). 346-350 (2001)
Yoshida A 等人:“类风湿性关节炎患者中放线杆菌伴放线菌 40 千道尔顿热休克蛋白的免疫优势区域”J Dent Res。
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41
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