Suppr超能文献

在暴露于2,3,7,8-四氯二苯并-对-二恶英(TCDD)后,芳烃受体上调hCMEC/D3人脑血管内皮细胞中的白细胞介素-1β(IL-1β)表达。

Aryl hydrocarbon receptor upregulates IL-1β expression in hCMEC/D3 human cerebral microvascular endothelial cells after TCDD exposure.

作者信息

Jacob Aude, Tomkiewicz-Raulet Céline, Jamet Charlotte, Bendayan Reina, Massicot France, Coumoul Xavier, Declèves Xavier

机构信息

INSERM, UMR-S 1144, Paris F-75006, France; Université Paris Descartes, UMR-S 1144, Paris F-75006, France; Université Paris Diderot, UMR-S 1144, Paris F-75013, France.

INSERM, UMR-S 1124, Toxicologie Pharmacologie et Signalisation cellulaire, 45 rue des Saints-Pères, 75006 Paris, France; Université Paris Descartes, ComUE Sorbonne Paris Cité, 45 rue des Saints-Pères, 75006 Paris, France.

出版信息

Toxicol In Vitro. 2017 Jun;41:200-204. doi: 10.1016/j.tiv.2017.03.001. Epub 2017 Mar 8.

Abstract

The AhR is a cytosolic ligand-dependent transcription factor activated by both endogenous and exogenous chemicals. It can regulate expression of many target genes including some inflammatory cytokines and chemokines. To date AhR implication in the regulation of inflammatory cytokines and chemokines at human cerebral endothelium has not been addressed. In the present study, we investigated whether AhR could regulate the expression of two pro-inflammatory cytokines and one chemokine i.e. IL-1β, IL-6 and IL-8 in the hCMEC/D3 human cerebral microvascular endothelial cell line. Exposure to TCDD increased IL-1β mRNA expression levels in hCMEC/D3. By using small interfering RNA against AhR we demonstrated that TCDD effects on IL-1β expression were mediated through AhR activation. Regarding IL-6 and IL-8, TCDD exposure had little or no effect on their mRNA levels in hCMEC/D3. In conclusion, our findings suggest that AhR-mediated IL-1β regulation in cerebral endothelium could induce BBB breakdown and contribute to the pathogenesis of a variety of neurologic disorders.

摘要

芳香烃受体(AhR)是一种胞质内依赖配体的转录因子,可被内源性和外源性化学物质激活。它能调节许多靶基因的表达,包括一些炎性细胞因子和趋化因子。迄今为止,AhR在人脑血管内皮细胞中对炎性细胞因子和趋化因子的调节作用尚未得到研究。在本研究中,我们调查了AhR是否能调节人脑血管微血管内皮细胞系hCMEC/D3中两种促炎细胞因子和一种趋化因子即白细胞介素-1β(IL-1β)、白细胞介素-6(IL-6)和白细胞介素-8(IL-8)的表达。暴露于2,3,7,8-四氯二苯并对二恶英(TCDD)可增加hCMEC/D3中IL-1β mRNA的表达水平。通过使用针对AhR的小干扰RNA,我们证明TCDD对IL-1β表达的影响是通过AhR激活介导的。关于IL-6和IL-8,TCDD暴露对hCMEC/D3中它们的mRNA水平几乎没有影响或没有影响。总之,我们的研究结果表明,AhR介导的脑血管内皮细胞中IL-1β调节可能导致血脑屏障破坏,并促成多种神经系统疾病的发病机制。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验