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首页> 外文期刊>Modern Rheumatology >CD40-CD40 ligand signal induces the intercellular adhesion molecule-1 expression through nuclear factor-kappa B p50 in cultured salivary gland epithelial cells from patients with Sj?gren's syndrome
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CD40-CD40 ligand signal induces the intercellular adhesion molecule-1 expression through nuclear factor-kappa B p50 in cultured salivary gland epithelial cells from patients with Sj?gren's syndrome

机译:CD40-CD40配体信号通过干燥综合征患者唾液腺上皮细胞中的核因子-κBp50诱导细胞间粘附分子-1表达

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摘要

The purpose of this study is to clarify signal transduction of expression of the intercellular adhesion molecule-1 (ICAM-1) via CD40-CD40 ligand in salivary glands of patients with Sj?gren's syndrome (SS). We used cultured salivary gland epithelial cells (SG cells) from 15 SS patients and 8 controls obtained by labial minor salivary gland biopsy. First, ICAM-1 expression was determined with reverse transcriptase–polymerase chain reaction and flow cytometry in the presence or absence of soluble CD40L (sCD40L). Next, SG cells were transfected with plasmids of pGL1.3-Luc inserted with promoter region of ICAM-1, pGL1.3kB?-Luc mutated in nuclear factor kappa-B (NF-κB) binding site of pGL1.3-Luc and pNF-κB-Luc by lipofection method. Luciferase activity of the cells was measured in the presence or absence of sCD40L or sCD40L and an NF-κB inhibitor, pyrrolidine dithiocarbamate (PDTC). Finally NF-κB family proteins of cell nuclear extracts were determined. ICAM-1 expression was significantly enhanced with sCD40L at the mRNA and protein level. Activity of pNF-κB-Luc and pGL1.3-Luc was significantly elevated by stimulation with sCD40L and suppressed by PDTC. NF-κB p50 protein level was elevated by stimulation with sCD40L and suppressed by PDTC. Our results suggest that sCD40L enhances the ICAM-1 expression by activation of NF-κB p50 in the SS SG cells.
机译:这项研究的目的是阐明干燥综合征患者唾液腺中CD40-CD40配体通过细胞间粘附分子1(ICAM-1)表达的信号转导。我们使用了来自15名SS患者和8名通过小口唇唾液腺活检获得的对照的唾液腺上皮细胞(SG细胞)。首先,在有或没有可溶性CD40L(sCD40L)的情况下,通过逆转录酶-聚合酶链反应和流式细胞仪确定ICAM-1的表达。接下来,用pGL1.3-Luc质粒转染SG细胞,该质粒插入了ICAM-1的启动子区域,即在pGL1的核因子κB(NF-κB)结合位点突变的pGL1.3kBα-Luc。通过脂质转染法制备3-Luc和pNF-κB-Luc。在存在或不存在sCD40L或sCD40L以及NF-κB抑制剂吡咯烷二硫代氨基甲酸酯(PDTC)的情况下测量细胞的萤光素酶活性。最后确定了细胞核提取物的NF-κB家族蛋白。 sCD40L在mRNA和蛋白水平上均显着增强了ICAM-1表达。 sCD40L刺激显着提高了pNF-κB-Luc和pGL1.3-Luc的活性,PDTC抑制了其活性。 sCD40L刺激可升高NF-κBp50蛋白水平,PDTC可抑制NF-κBp50蛋白水平。我们的结果表明,sCD40L通过激活SS SG细胞中的NF-κBp50来增强ICAM-1表达。

著录项

  • 来源
    《Modern Rheumatology》 |2007年第1期|45-53|共9页
  • 作者单位

    Third Department of Internal Medicine Hamamatsu University School of Medicine 1-20-1 Handayama Hamamatsu 431-3192 Japan;

    Third Department of Internal Medicine Hamamatsu University School of Medicine 1-20-1 Handayama Hamamatsu 431-3192 Japan;

    Omaezaki Municipal Hospital Shizuoka Japan;

    Third Department of Internal Medicine Hamamatsu University School of Medicine 1-20-1 Handayama Hamamatsu 431-3192 Japan;

    Third Department of Internal Medicine Hamamatsu University School of Medicine 1-20-1 Handayama Hamamatsu 431-3192 Japan;

    Third Department of Internal Medicine Hamamatsu University School of Medicine 1-20-1 Handayama Hamamatsu 431-3192 Japan;

    Third Department of Internal Medicine Hamamatsu University School of Medicine 1-20-1 Handayama Hamamatsu 431-3192 Japan;

    Third Department of Internal Medicine Hamamatsu University School of Medicine 1-20-1 Handayama Hamamatsu 431-3192 Japan;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    CD40 ligand; Intercellular adhesion molecule-1; Nuclear factor-kappa B; Salivary gland epithelial cells; Sj?gren's syndrome;

    机译:CD40配体;细胞间黏附分子-1;核因子-κB;唾液腺上皮细胞;干燥综合征;

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