Qian Ya-Jie, Wang Xiang, Gao Ya-Fan, Duan Ning, Huang Xiao-Feng, Sun Fang-Fang, Han Xiao-Dong, Wang Wen-Mei
Department of Oral Medicine, Nanjing Stomatological Hospital, Medical School of Nanjing University, Nanjing, China.
Cell Physiol Biochem. 2015;36(2):457-73. doi: 10.1159/000430112. Epub 2015 May 11.
BACKGROUND/AIMS: Nucleotide binding oligomerization domain 1 (NOD1) signal pathway and human β defensins (hBDs) play crucial roles in innate immune. Cigarette smoke has been confirmed to dampen innate immune in some human tissues, such as oral mucosa. The aim of this study was to evaluate potential effects of smoking on NOD1 signaling and hBDs expression in oral mucosa.
Tissue specimens of normal oral mucosa were collected from donors undergoing routine surgical treatment. All 20 participants were classified equally as two groups: non-smokers and smokers. By using Western blotting and immunohistochemistry, we investigated differential expression of crucial molecules in NOD1 signal pathway, hBD-1, -2, and -3 in oral mucosa tissues between non-smokers and smokers. Immortalized human oral mucosal epithelial (Leuk-1) cells were treated with various concentrations of cigarette smoke extract (CSE) for 24h. Western blotting and immunofluorescence assays were performed to study CSE-induced alteration of protein expression. Leuk-1 cells were treated with 4% CSE, iE-DAP (NOD1 agonist), CSE + iE-DAP, BAY 11-7082 (NF-κB inhibitor), 4% CSE + BAY 11-7082, respectively. Real-time PCR and ELISA were performed to detect the mRNA levels and secretion of hBD-1, -2, and -3, respectively.
The levels of NOD1, NF-κB, hBD-1 and hBD-3 significantly reduced in oral mucosa tissues of smokers compared with non-smokers. The levels of RIP2 (receptor-interacting protein 2), phospho-NF-κB (P-NF-κB) and hBD-2 remarkably enhanced in oral mucosal tissues of smokers. CSE treatment suppressed NOD1 and NF-κB expression and activated RIP2 and P-NF-κB expression in Leuk-1 cells. The mRNA and secretory levels of hBD-1 and -3 were down-regulated by CSE, while the mRNA and secretory level of hBD-2 were up-regulated by CSE. The iE-DAP or BAY 11-7082 treatment reversed the regulatory effects of CSE on levels of hBDs.
The present study indicated that cigarette smoke could potentially modulate the expression of crucial molecules of NOD1 signal pathway and hBDs in human oral mucosal epithelium. NOD1 signal pathway could play an important role in the regulatory effects of CSE on hBDs levels in oral mucosal epithelial cells.
背景/目的:核苷酸结合寡聚化结构域1(NOD1)信号通路和人β防御素(hBDs)在先天免疫中发挥关键作用。香烟烟雾已被证实在某些人体组织(如口腔黏膜)中会削弱先天免疫。本研究旨在评估吸烟对口腔黏膜中NOD1信号和hBDs表达的潜在影响。
从接受常规外科治疗的供体中收集正常口腔黏膜组织标本。20名参与者被平均分为两组:非吸烟者和吸烟者。通过蛋白质印迹法和免疫组织化学,我们研究了非吸烟者和吸烟者口腔黏膜组织中NOD1信号通路关键分子、hBD-1、-2和-3的差异表达。用不同浓度的香烟烟雾提取物(CSE)处理永生化的人口腔黏膜上皮(Leuk-1)细胞24小时。进行蛋白质印迹法和免疫荧光分析以研究CSE诱导的蛋白质表达变化。分别用4% CSE、iE-DAP(NOD1激动剂)、CSE + iE-DAP、BAY 11-7082(NF-κB抑制剂)、4% CSE + BAY 11-7082处理Leuk-1细胞。进行实时定量聚合酶链反应(Real-time PCR)和酶联免疫吸附测定(ELISA)分别检测hBD-1、-2和-3的mRNA水平和分泌情况。
与非吸烟者相比,吸烟者口腔黏膜组织中NOD1、NF-κB、hBD-1和hBD-3的水平显著降低。吸烟者口腔黏膜组织中受体相互作用蛋白2(RIP2)、磷酸化NF-κB(P-NF-κB)和hBD-2的水平显著升高。CSE处理抑制了Leuk-1细胞中NOD1和NF-κB的表达,并激活了RIP2和P-NF-κB的表达。CSE下调了hBD-1和-3的mRNA及分泌水平,而CSE上调了hBD-2的mRNA及分泌水平。iE-DAP或BAY 11-7082处理逆转了CSE对hBDs水平的调节作用。
本研究表明,香烟烟雾可能会调节人口腔黏膜上皮中NOD1信号通路关键分子和hBDs的表达。NOD1信号通路可能在CSE对口腔黏膜上皮细胞中hBDs水平的调节作用中发挥重要作用。