Suppr超能文献

人类单核细胞和巨噬细胞中的芳烃受体/二噁英受体。

Aryl hydrocarbon receptor/dioxin receptor in human monocytes and macrophages.

作者信息

Komura K, Hayashi S, Makino I, Poellinger L, Tanaka H

机构信息

Second Department of Internal Medicine, Asahikawa Medical College, Midorigaoka Higashi, Japan.

出版信息

Mol Cell Biochem. 2001 Oct;226(1-2):107-18. doi: 10.1023/a:1012762519424.

Abstract

Aryl hydrocarbon receptor (AhR) belongs to the bHLH/PAS transcription factor family and is activated by various polycyclic or halogenated aromatic hydrocarbons, e.g. 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), 3-methylcholanthrene (3MC). In the present study, we showed that in U937 cells and human macrophages AhR, with its partner cofactor Arnt, is expressed and CYP1A1 mRNA expression is induced in the presence of AhR ligand 3MC. Moreover, we showed that AhR, associating with Arnt, binds to target DNA sequences and activates transcription. Since part of AhR is activated into DNA binding species in the absence of exogenous ligand and competitive AhR antagonist alpha-naphthoflavone inhibits this activation process with reducing CYP1A1 mRNA expression levels, the presence of endogenous ligand is indicated.

摘要

芳烃受体(AhR)属于bHLH/PAS转录因子家族,可被多种多环或卤代芳烃激活,例如2,3,7,8-四氯二苯并对二恶英(TCDD)、3-甲基胆蒽(3MC)。在本研究中,我们发现,在U937细胞和人类巨噬细胞中,AhR与其伴侣辅因子Arnt共同表达,并且在AhR配体3MC存在的情况下,CYP1A1 mRNA表达被诱导。此外,我们还发现,AhR与Arnt结合,可与靶DNA序列结合并激活转录。由于在没有外源性配体的情况下,部分AhR会被激活形成DNA结合形式,且竞争性AhR拮抗剂α-萘黄酮可通过降低CYP1A1 mRNA表达水平来抑制这一激活过程,因此表明存在内源性配体。

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