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脂多糖刺激牙龈成纤维细胞产生白细胞介素11、6的研究
引用本文:和璐,長澤敏行,石川烈. 脂多糖刺激牙龈成纤维细胞产生白细胞介素11、6的研究[J]. 中华口腔医学杂志, 2007, 42(1): 34-36
作者姓名:和璐  長澤敏行  石川烈
作者单位:1. 100081,北京大学口腔医学院·口腔医院牙周科
2. 東京醫科齒科大學齒周病分野
摘    要:
目的观察牙龈卟啉单胞菌(Porphyromonas gingivalis,Pg)、伴放线放线杆菌(Actinobacillus actinomycetemcomitans,Aa)、大肠杆菌(Escherichia coli,Ec)的脂多糖(lipopolysacchrides,LPS)刺激人牙龈成纤维细胞(human gingival fibroblasts,HGF)合成白细胞介素(interleukin,IL)-11和IL-6的能力,并了解内源性前列腺素是否介导IL-11和IL-6的产生。方法将3种浓度的LPS(0.1、1、10mg/L)分别作用于体外培养的HGF 24h,另外在10mg/L的LPS中加入10^-6 moL/L的吲哚美辛后再分别刺激HGF 24h,ELISA法检测HGF上清液中IL-11和IL-6含量的变化。结果Aa-,Ec-LPS(10mg/L)和Pg-LPS(1、10mg/L)刺激HGF后IL-11水平显著提高;Pg-,Ec-LPS(0.1、1、10mg/L)和Aa-LPS(1、10ms/L)刺激HGF产生IL-6的水平明显增高;这些作用均受到吲哚美辛的抑制作用。结论LPS使HGF产生IL-11和IL-6的水平明显增加,并受到内源性前列腺素的正向调控。

关 键 词:脂多糖类 白细胞介素11 白细胞介素6 紫单胞菌 龈
收稿时间:2006-06-30
修稿时间:2006-06-30

Production of interleukin-11 and interleukin-6 in cultured human gingival fibroblasts with the stimulation of lipopolysacchrides
HE Lu,Nagasawa Toshiyuki,Ishikawa Isao. Production of interleukin-11 and interleukin-6 in cultured human gingival fibroblasts with the stimulation of lipopolysacchrides[J]. Chinese journal of stomatology, 2007, 42(1): 34-36
Authors:HE Lu  Nagasawa Toshiyuki  Ishikawa Isao
Affiliation:Department of Periodontology , Peking University School and Hospital of Stomatology , Beijing 100081, China
Abstract:
OBJECTIVE: To observe the effects of Porphyromonas gingivalis (Pg), Actinobacillus actinomycetemcomitans (Aa), Escherichia coli (Ec) lipopolysacchrides (LPS) on the production of IL-11 and IL-6 from healthy human gingival fibroblasts (HGF), and the effects of endogenous prostaglandin on HGF IL-11 and IL-6 production stimulated with the above LPS. METHODS: HGF were stimulated with Pg-, Aa-, Ec-LPS of different concentrations (0.1, 1, 10 mg/L) for 24 h. And HGF were also stimulated with the combinations of 10 mg/L Pg-, Aa-, Ec-LPS and 10(-6) mol/L indomethacin respectively for 24 h. Levels of IL-11 and IL-6 in the supernatants were quantitated by ELISA. RESULTS: LPS from Aa, Ec, at the concentration of 10 mg/L and from Pg at the concentrations 1, 10 mg/L significantly augmented IL-11 production by HGF. IL-6 production was also significantly increased by stimulation with Aa-LPS at concentrations 1, 10 mg/L and with Ec-, Pg-LPS at concentrations 0.1, 1, 10 mg/L. In addition, IL-11 production was lower than IL-6 production by HGF stimulated with LPS. Indomethacin significantly inhibited IL-6 and IL-11 production in LPS-stimulated HGF. CONCLUSIONS: Aa-, Pg-, Ec-LPS may significantly increase IL-11 and IL-6 level in the supernatants of HGF, and endogenous prostaglandin may upregulate IL-11 and IL-6 production in LPS-stimulated HGF.
Keywords:Lipopolysaccharides   Interleukin-11    Interleukin-6    Porphyromonas gingivalis
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