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长期高脂肪饮食诱导肥胖后 Nrf2 敲除小鼠的肝脏基因表达谱。

Hepatic gene expression profiling in Nrf2 knockout mice after long-term high-fat diet-induced obesity.

机构信息

Division of Endocrinology, Department of Internal Medicine, Medical School, University of Patras, 26504 Patras, Greece.

出版信息

Oxid Med Cell Longev. 2013;2013:340731. doi: 10.1155/2013/340731. Epub 2013 Apr 18.

Abstract

INTRODUCTION

The transcription factor NFE2-related factor 2 (Nrf2) is a central regulator of antioxidant and detoxification gene expression in response to electrophilic or oxidative stress. Nrf2 has recently been shown to cross-talk with metabolic pathways, and its gene deletion protected mice from high-fat-diet-(HFD-) induced obesity and insulin resistance. This study aimed to identify potential Nrf2-regulated genes of metabolic interest by comparing gene expression profiles of livers of wild-type (WT) versus Nrf2 knockout (Nrf2-KO) mice after a long-term HFD.

METHODS

WT and Nrf2-KO mice were fed an HFD for 180 days; total RNA was prepared from liver and used for microarray analysis and quantitative real-time RT-PCR (qRT-PCR).

RESULTS

The microarray analysis identified 601 genes that were differentially expressed between WT and Nrf2-KO mice after long-term HFD. Selected genes, including ones known to be involved in metabolic regulation, were prioritized for verification by qRT-PCR: Cyp7a1 and Fabp5 were significantly overexpressed in Nrf2-KO mice; in contrast, Car, Cyp2b10, Lipocalin 13, Aquaporin 8, Cbr3, Me1, and Nqo1 were significantly underexpressed in Nrf2-KO mice.

CONCLUSION

Transcriptome profiling after HFD-induced obesity confirms that Nrf2 is implicated in liver metabolic gene networks. The specific genes identified here may provide insights into Nrf2-dependent mechanisms of metabolic regulation.

摘要

简介

转录因子 NFE2 相关因子 2(Nrf2)是一种重要的抗氧化和解毒基因表达的调节剂,可响应亲电或氧化应激。最近研究表明,Nrf2 与代谢途径相互作用,其基因缺失可保护小鼠免受高脂肪饮食(HFD)诱导的肥胖和胰岛素抵抗。本研究旨在通过比较长期 HFD 后野生型(WT)和 Nrf2 敲除(Nrf2-KO)小鼠肝脏的基因表达谱,来鉴定代谢相关的潜在 Nrf2 调控基因。

方法

WT 和 Nrf2-KO 小鼠喂食 HFD 180 天;从肝脏中提取总 RNA,用于微阵列分析和定量实时 RT-PCR(qRT-PCR)。

结果

微阵列分析鉴定出 601 个在长期 HFD 后 WT 和 Nrf2-KO 小鼠之间差异表达的基因。选择了一些已知参与代谢调节的基因,通过 qRT-PCR 对其进行了优先验证:Cyp7a1 和 Fabp5 在 Nrf2-KO 小鼠中表达显著上调;相反,Car、Cyp2b10、Lipocalin 13、Aquaporin 8、Cbr3、Me1 和 Nqo1 在 Nrf2-KO 小鼠中表达显著下调。

结论

HFD 诱导肥胖后的转录组谱分析证实,Nrf2 参与肝脏代谢基因网络。这里鉴定的特定基因可能为 Nrf2 依赖的代谢调节机制提供了一些见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d48e/3654373/33e02b306ad5/OXIMED2013-340731.001.jpg

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