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牙龈卟啉单胞菌菌毛诱导小鼠腹腔巨噬细胞中性粒细胞趋化因子KC基因的表达:蛋白激酶C的作用

Porphyromonas gingivalis fimbriae induce expression of the neutrophil chemotactic factor KC gene of mouse peritoneal macrophages: role of protein kinase C.

作者信息

Hanazawa S, Murakami Y, Takeshita A, Kitami H, Ohta K, Amano S, Kitano S

机构信息

Department of Oral Microbiology, Meikai University School of Dentistry, Saitama, Japan.

出版信息

Infect Immun. 1992 Apr;60(4):1544-9. doi: 10.1128/iai.60.4.1544-1549.1992.

Abstract

To account for infiltration of the periodontal tissues by neutrophils, the present study was undertaken to examine whether Porphyromonas gingivalis fimbriae, important structures involved in attachment of the bacteria to periodontal tissues, induce gene expression of the neutrophil chemoattractant KC in macrophages. The fimbriae induced expression of the KC gene of mouse peritoneal macrophages in a dose-dependent fashion. The peak of KC gene expression was observed as early as 1 h after initiation of the treatment. However, the gene expression was short lived, with the expression decreasing gradually after 6 h. A nuclear transcriptional assay showed that the fimbriae regulated the KC gene expression at a posttranscriptional level. We observed that the fimbria-induced KC gene expression was not regulated by endogenous or exogenous prostaglandin. Furthermore, forskolin, a potent activator of adenyl cyclase, and dibutyryl cyclic AMP were incapable of inducing KC gene expression of the peritoneal macrophages. H-8 and HA 1004, inhibitors of cyclic nucleotide-dependent protein kinases, had little effect on the fimbria-induced KC gene expression. On the other hand, the fimbria-induced KC gene expression was inhibited markedly by treatment with H-7, a potent inhibitor of protein kinase C. We also observed that phorbol 12-myristate 13-acetate, a specific activator of protein kinase C, induced KC gene expression of peritoneal macrophages in a dose-dependent fashion. In addition, the fimbria-induced KC gene expression was suppressed in the peritoneal macrophages pretreated for 24 h with phorbol 12-myristate 13-acetate. These results suggest that the KC gene expression was mediated through activation of protein kinase C and not through that of cyclic nucleotide-dependent protein kinases. The present study indicates that P. gingivalis fimbriae can induce gene expression of the neutrophil chemotactic factor KC by macrophages via protein kinase C and suggests that this factor may be involved in infiltration of neutrophils into the periodontal tissues of adult periodontal patients.

摘要

为了解释中性粒细胞对牙周组织的浸润情况,本研究旨在检测牙龈卟啉单胞菌菌毛(该细菌附着于牙周组织的重要结构)是否会诱导巨噬细胞中中性粒细胞趋化因子KC的基因表达。菌毛以剂量依赖的方式诱导小鼠腹腔巨噬细胞KC基因的表达。早在治疗开始后1小时就观察到KC基因表达的峰值。然而,该基因表达持续时间较短,6小时后表达逐渐下降。一项核转录分析表明,菌毛在转录后水平调节KC基因的表达。我们观察到,菌毛诱导的KC基因表达不受内源性或外源性前列腺素的调节。此外,腺苷酸环化酶的强效激活剂福斯可林和二丁酰环磷腺苷不能诱导腹腔巨噬细胞的KC基因表达。环核苷酸依赖性蛋白激酶抑制剂H-8和HA 1004对菌毛诱导的KC基因表达几乎没有影响。另一方面,蛋白激酶C的强效抑制剂H-7处理可显著抑制菌毛诱导的KC基因表达。我们还观察到,蛋白激酶C的特异性激活剂佛波酯12-肉豆蔻酸酯13-乙酸盐以剂量依赖的方式诱导腹腔巨噬细胞的KC基因表达。此外,用佛波酯12-肉豆蔻酸酯13-乙酸盐预处理24小时的腹腔巨噬细胞中,菌毛诱导的KC基因表达受到抑制。这些结果表明,KC基因表达是通过蛋白激酶C的激活介导的,而不是通过环核苷酸依赖性蛋白激酶的激活介导的。本研究表明,牙龈卟啉单胞菌菌毛可通过蛋白激酶C诱导巨噬细胞表达中性粒细胞趋化因子KC,并提示该因子可能参与成年牙周炎患者牙周组织中中性粒细胞的浸润。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c341/257029/702a98add421/iai00028-0295-a.jpg

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