首页> 外文期刊>Toxicological sciences: An official journal of the Society of Toxicology >HMOX1 and NQO1 genes are upregulated in response to contact sensitizers in dendritic cells and THP-1 cell line: role of the Keap1/Nrf2 pathway.
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HMOX1 and NQO1 genes are upregulated in response to contact sensitizers in dendritic cells and THP-1 cell line: role of the Keap1/Nrf2 pathway.

机译:HMOX1和NQO1基因上调响应树突状细胞和THP-1细胞系中的接触敏化剂:Keap1 / Nrf2途径的作用。

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摘要

Electrophilicity is one of the most common features of skin contact sensitizers and is necessary for protein haptenation. The Keap1 (Kelch-like ECH-associated protein 1)/Nrf2 -signaling pathway is dedicated to the detection of electrophilic stress in cells leading to the upregulation of genes involved in protection or neutralization of chemical reactive species. Signals provided by chemical stress could play an important role in dendritic cell activation and the aim of this work was to test whether contact sensitizers were specific activators of the Keap1/Nrf2 pathway. CD34-derived dendritic cells (CD34-DC) and the THP-1 myeloid cell line were treated by a panel of sensitizers (Ni, 1-chloro 2,4-dinitrobenzene, cinnamaldehyde, 7-hydroxycitronellal, 1,4-dihydroquinone, alpha-methyl-trans-cinnamaldehyde, 2-4-tert-(butylbenzyl)propionaldehyde or Lilial, and 1,4-phenylenediamine), irritants (sodium dodecyl sulfate, benzalkonium chloride), and a nonsensitizer molecule (chlorobenzene). Three well-known Nrf2 activators (tert-butylhydroquinone, lipoic acid, sulforaphane) were also tested. Expression of hmox1 and nqo1 was measured using real-time PCR and cellular accumulation of Nrf2 was assessed by Western blot. Our results showed an increased expression at early time points of hmox1 and nqo1 mRNAs in response to sensitizers but not to irritants. Accumulation of the Nrf2 protein was also observed only with chemical sensitizers. A significant inhibition of the expression of hmox1 and nqo1 mRNAs and CD86 expression was found in 1-chloro 2,4-dinitrobenzene-treated THP-1 cells preincubated with N-acetyl cysteine, a glutathione precursor. Altogether, these data suggested that the Keap1/Nrf2-signaling pathway was activated by electrophilic molecules including sensitizers in dendritic cells and in the THP-1 cell line. Monitoring of this pathway may provide new biomarkers (e.g., Nrf2, hmox1) for the detection of the sensitization potential of chemicals.
机译:亲电性是皮肤接触敏化剂的最常见特征之一,也是蛋白质半抗原化所必需的。 Keap1(类似于Kelch的ECH相关蛋白1)/ Nrf2信号通路专门用于检测细胞中的亲电子应激,从而导致参与保护或中和化学反应性物种的基因上调。化学应激提供的信号可能在树突状细胞激活中起重要作用,这项工作的目的是测试接触敏化剂是否为Keap1 / Nrf2途径的特异性激活剂。 CD34衍生的树突状细胞(CD34-DC)和THP-1髓样细胞系用一组敏化剂(Ni,1-氯2,4-二硝基苯,肉桂醛,7-羟基香茅醛,1,4-二氢醌,α -甲基-反式肉桂醛,2--4-叔-(丁基苄基)丙醛或Lialal和1,4-苯二胺),刺激物(十二烷基硫酸钠,苯扎氯铵)和非敏化剂分子(氯苯)。还测试了三种著名的Nrf2活化剂(叔丁基对苯二酚,硫辛酸,萝卜硫烷)。使用实时PCR测量hmox1和nqo1的表达,并通过蛋白质印迹评估Nrf2的细胞积累。我们的研究结果表明,响应敏化剂而不刺激刺激物,hmox1和nqo1 mRNA的早期表达增加。仅使用化学敏化剂也观察到Nrf2蛋白的积累。在用谷胱甘肽前体N-乙酰基半胱氨酸预孵育的1-氯2,4-二硝基苯处理的THP-1细胞中,发现hmox1和nqo1 mRNA的表达以及CD86表达受到显着抑制。总之,这些数据表明Keap1 / Nrf2信号通路被树状细胞和THP-1细胞系中的包括敏化剂在内的亲电分子激活。对该途径的监测可能会提供新的生物标记(例如Nrf2,hmox1),以检测化学物质的致敏性。

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