1[2-氰-3,12-二氧齐烷-1,9(11)-二烯-28-油基]咪唑诱导人内皮细胞保护的时间过程表达分析。

Gene regulation and systems biology Pub Date : 2017-04-07 eCollection Date: 2017-01-01 DOI:10.1177/1177625017701106
James A Bynum, Xinyu Wang, Salomon A Stavchansky, Phillip D Bowman
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引用次数: 3

摘要

1[2-氰-3,12-二氧齐墩酸-1,9(11)-二氧齐墩酸-28-油基]咪唑(CDDO-Im)是齐墩果酸的合成衍生物,在几种动物和体外模型中显示出抗氧化和抗炎活性,已被证明在损伤后给予有益。虽然血红素加氧酶1的诱导似乎是细胞保护的主要效应,但其整体效应的介导机制在很大程度上是未知的。本研究评估了时间基因表达谱,以更好地表征人类脐静脉内皮细胞(HUVEC)对CDDO-Im的早期转录事件及其与细胞保护反应动力学的关系。用CDDO-Im处理HUVEC 0.5、1、3、6和24小时,进行时间过程基因表达谱分析。在整个时间过程中,至少有1万个基因的表达在统计上发生了改变。在给药后0.5小时内,立即早期基因表达的大变化很容易检测到。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Time Course Expression Analysis of 1[2-cyano-3,12-dioxooleana-1,9(11)-dien-28-oyl]imidazole Induction of Cytoprotection in Human Endothelial Cells.

1[2-cyano-3,12-dioxooleana-1,9(11)-dien-28-oyl]imidazole (CDDO-Im), a synthetic derivative of oleanolic acid that exhibits antioxidant and anti-inflammatory activity in several animal and in vitro models, has been shown to be beneficial if given after injury. Although induction of heme oxygenase 1 appears to be a major effector of cytoprotection, the mechanism by which the overall effect is mediated is largely unknown. This study evaluated temporal gene expression profiles to better characterize the early transcriptional events and their relationship to the dynamics of the cytoprotective response in human umbilical vein endothelial cells (HUVEC) to CDDO-Im. Time-course gene expression profiling was performed on HUVEC treated with CDDO-Im for 0.5, 1, 3, 6, and 24 hours. More than 10 000 genes were statistically altered in their expression in at least 1 time point across the time course. Large alterations in immediate-early gene expression were readily detectable within 0.5 hour after administration of CDDO-Im.

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