Tabuchi Yoshiaki, Yunoki Tatsuya, Hoshi Nobuhiko, Suzuki Nobuo, Kondo Takashi
Division of Molecular Genetics Research, Life Science Research Center, University of Toyama, 2630 Sugitani, Toyama 930-0194, Japan.
Department of Radiological Sciences, Graduate School of Medicine and Pharmaceutical Sciences, University of Toyama, 2630 Sugitani, Toyama 930-0194, Japan.
Int J Mol Sci. 2014 May 20;15(5):8959-78. doi: 10.3390/ijms15058959.
Here, to understand the molecular mechanisms underlying cell death induced by sodium fluoride (NaF), we analyzed gene expression patterns in rat oral epithelial ROE2 cells exposed to NaF using global-scale microarrays and bioinformatics tools. A relatively high concentration of NaF (2 mM) induced cell death concomitant with decreases in mitochondrial membrane potential, chromatin condensation and caspase-3 activation. Using 980 probe sets, we identified 432 up-regulated and 548 down-regulated genes, that were differentially expressed by >2.5-fold in the cells treated with 2 mM of NaF and categorized them into 4 groups by K-means clustering. Ingenuity® pathway analysis revealed several gene networks from gene clusters. The gene networks Up-I and Up-II included many up-regulated genes that were mainly associated with the biological function of induction or prevention of cell death, respectively, such as Atf3, Ddit3 and Fos (for Up-I) and Atf4 and Hspa5 (for Up-II). Interestingly, knockdown of Ddit3 and Hspa5 significantly increased and decreased the number of viable cells, respectively. Moreover, several endoplasmic reticulum (ER) stress-related genes including, Ddit3, Atf4 and Hapa5, were observed in these gene networks. These findings will provide further insight into the molecular mechanisms of NaF-induced cell death accompanying ER stress in oral epithelial cells.
在此,为了解氟化钠(NaF)诱导细胞死亡的分子机制,我们使用全基因组微阵列和生物信息学工具分析了暴露于NaF的大鼠口腔上皮ROE2细胞中的基因表达模式。相对高浓度的NaF(2 mM)诱导细胞死亡,同时伴有线粒体膜电位降低、染色质浓缩和半胱天冬酶-3激活。我们使用980个探针集,鉴定出432个上调基因和548个下调基因,这些基因在用2 mM NaF处理的细胞中差异表达超过2.5倍,并通过K均值聚类将它们分为4组。Ingenuity®通路分析从基因簇中揭示了几个基因网络。基因网络Up-I和Up-II分别包含许多上调基因,它们主要分别与诱导或预防细胞死亡的生物学功能相关,例如Atf3、Ddit3和Fos(对于Up-I)以及Atf4和Hspa5(对于Up-II)。有趣的是,敲低Ddit3和Hspa5分别显著增加和减少了活细胞数量。此外,在这些基因网络中观察到了几个与内质网(ER)应激相关的基因,包括Ddit3、Atf4和Hapa5。这些发现将为深入了解NaF诱导口腔上皮细胞中伴随ER应激的细胞死亡的分子机制提供进一步的见解。