Gon Yasuhiro, Maruoka Shuichiro, Kishi Hiroyuki, Kozu Yutaka, Kazumichi Kuroda, Nomura Yasuyuki, Takeshita Ikuko, Oshima Takeshi, Hashimoto Shu
Division of Respiratory Medicine, Nihon University School of Medicine, 30-1 Ohyaguchi-Kamicho, Itabashiku, Tokyo 173-8610, Japan.
Division of Otolaryngology, Nihon University School of Medicine, 30-1 Ohyaguchi-Kamicho, Itabashiku, Tokyo 173-8610, Japan.
Cell Biol Int. 2017 Jul;41(7):716-725. doi: 10.1002/cbin.10741. Epub 2017 Mar 10.
Impairment of epithelial barrier integrity caused by environmental triggers is associated with the pathogenesis of airway inflammation. Using human airway epithelial cells, we attempted to identify molecule(s) that promote airway epithelial barrier integrity. Microarray analyses were conducted using the Affimetrix human whole genome gene chip, and we identified the N-myc downstream-regulated gene 1 (NDRG1) gene, which was induced during the development of the epithelial cell barrier. Immunohistochemical analysis revealed strong NDRG1 expression in ciliated epithelial cells in nasal tissues sampled from patients with chronic rhinosinusitis (CRS), and the low expression of NDRG1 was observed in goblet cells or damaged epithelial cells. NDRG1 gene knockdown with its specific siRNA decreased the transepithelial electrical resistance and increased the dextran permeability. Immunocytochemistry revealed that NDRG1 knockdown disrupted tight junctions of airway epithelial cells. Next, we analyzed the effects of NDRG1 knockdown on the expression of tight and adhesion junction molecules. NDRG1 knockdown significantly decreased only claudin-9 expression, but did not decrease other claudin family molecules, such as E-cadherin, and ZO-1, -2, or -3. Knockdown of claudin-9 markedly impaired the barrier function in airway epithelial cells. These results suggest that NDRG1 is important for the barrier integrity in airway epithelial cells.
环境触发因素导致的上皮屏障完整性受损与气道炎症的发病机制相关。我们使用人气道上皮细胞,试图鉴定促进气道上皮屏障完整性的分子。使用Affimetrix人类全基因组基因芯片进行微阵列分析,我们鉴定出N- myc下游调控基因1(NDRG1)基因,该基因在上皮细胞屏障形成过程中被诱导。免疫组织化学分析显示,在慢性鼻-鼻窦炎(CRS)患者的鼻组织中,纤毛上皮细胞中有强烈的NDRG1表达,而在杯状细胞或受损上皮细胞中观察到NDRG1低表达。用其特异性siRNA敲低NDRG1基因会降低跨上皮电阻并增加右旋糖酐通透性。免疫细胞化学显示,NDRG1敲低会破坏气道上皮细胞的紧密连接。接下来,我们分析了NDRG1敲低对紧密连接和黏附连接分子表达的影响。NDRG1敲低仅显著降低了claudin-9的表达,但未降低其他claudin家族分子的表达,如E-钙黏蛋白以及ZO-1、ZO-2或ZO-3。敲低claudin-9会显著损害气道上皮细胞的屏障功能。这些结果表明,NDRG1对气道上皮细胞的屏障完整性很重要。