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参与氟化钠引发的口腔上皮细胞内质网应激伴细胞死亡的基因和基因网络。

Genes and gene networks involved in sodium fluoride-elicited cell death accompanying endoplasmic reticulum stress in oral epithelial cells.

作者信息

Tabuchi Yoshiaki, Yunoki Tatsuya, Hoshi Nobuhiko, Suzuki Nobuo, Kondo Takashi

机构信息

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.

出版信息

Int J Mol Sci. 2014 May 20;15(5):8959-78. doi: 10.3390/ijms15058959.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d49/4057769/5a9ca6b74b1f/ijms-15-08959f1.jpg

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