α -生育酚可调节肿瘤坏死因子α (TNF-α)诱导的牛细胞炎症反应的转录活性。

Gene regulation and systems biology Pub Date : 2012-01-01 Epub Date: 2011-12-05 DOI:10.4137/GRSB.S8303
Cong-Jun Li, Robert W Li, Stanislaw Kahl, Theodore H Elsasser
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引用次数: 8

摘要

为了进一步研究α-生育酚在维持牛细胞(Madin-Darby牛肾上皮细胞系)免疫稳态中的潜在作用,我们进行了体外实验,使用重组TNF-α作为免疫刺激剂,模拟α-生育酚预处理或不预处理的细胞的炎症反应。利用微阵列全局分析和IPA (Ingenuity Pathways Analysis, Ingenuity(®)Systems, http://www.ingenuity.com)数据分析这些细胞中TNF-α诱导的基因扰动,我们专注于确定在标准细胞培养条件下α-生育酚处理正常牛细胞是否可以改变TNF-α刺激诱导的细胞免疫反应。使用IPA对三个数据集进行筛选比较,三个数据集共有1750个基因可供比较,其中97个基因在三个数据集中都是共有的;615个基因在至少两个数据集中是常见的;TNF-α刺激组有261个特异基因,α-生育酚处理组有399个特异基因,α-生育酚加TNF-α处理组有378个特异基因。TNF-α激发引起基因表达的显著变化。TNF-α诱导的许多基因与细胞免疫和炎症反应有关。IPA数据分析结果显示,细胞α-生育酚预处理可调节细胞对TNF-α的应答。在大多数典型途径中,α-生育酚预处理对TNF-α-诱导的促炎反应具有拮抗作用。我们得出结论,α-生育酚预处理具有显著的拮抗作用,通过改变一些重要信号分子的基因表达活性来调节细胞对TNF-α的反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Alpha-Tocopherol Alters Transcription Activities that Modulates Tumor Necrosis Factor Alpha (TNF-α) Induced Inflammatory Response in Bovine Cells.

Alpha-Tocopherol Alters Transcription Activities that Modulates Tumor Necrosis Factor Alpha (TNF-α) Induced Inflammatory Response in Bovine Cells.

Alpha-Tocopherol Alters Transcription Activities that Modulates Tumor Necrosis Factor Alpha (TNF-α) Induced Inflammatory Response in Bovine Cells.

Alpha-Tocopherol Alters Transcription Activities that Modulates Tumor Necrosis Factor Alpha (TNF-α) Induced Inflammatory Response in Bovine Cells.

To further investigate the potential role of α-tocopherol in maintaining immuno-homeostasis in bovine cells (Madin-Darby bovine kidney epithelial cell line), we undertook in vitro experiments using recombinant TNF-α as an immuno-stimulant to simulate inflammation response in cells with or without α-tocopherol pre-treatment. Using microarray global-profiling and IPA (Ingenuity Pathways Analysis, Ingenuity(®) Systems, http://www.ingenuity.com) data analysis on TNF-α-induced gene perturbation in those cells, we focused on determining whether α-tocopherol treatment of normal bovine cells in a standard cell culture condition can modify cell's immune response induced by TNF-α challenge. When three datasets were filtered and compared using IPA, there were a total of 1750 genes in all three datasets for comparison, 97 genes were common in all three sets; 615 genes were common in at least two datasets; there were 261 genes unique in TNF-α challenge, 399 genes were unique in α-tocopherol treatment, and 378 genes were unique in the α-tocopherol plus TNF-α treatment. TNF-α challenge induced significant change in gene expression. Many of those genes induced by TNF-α are related to the cells immune and inflammatory responses. The results of IPA data analysis showed that α-tocopherol-pretreatment of cells modulated cell's response to TNF-α challenge. In most of the canonical pathways, α-tocopherol pretreatment showed the antagonistic effect against the TNF-α-induced pro-inflammatory responses. We concluded that α-tocopherol pre-treatment has a significant antagonistic effect that modulates the cell's response to the TNF-α challenge by altering the gene expression activities of some important signaling molecules.

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