Aryl hydrocarbon receptor/dioxin receptor in human monocytes and macrophages

被引:3
|
作者
Keiji Komura
Shin-ichi Hayashi
Isao Makino
Lorenz Poellinger
Hirotoshi Tanaka
机构
[1] Asahikawa Medical College,Second Department of Internal Medicine
[2] Saitama Cancer Center Research Institute,Division of Endocrinology
[3] Medical Nobel Institute,Department of Cell and Molecular Biology
[4] Karolinska Institute,Division of Clinical Immunology, Advanced Clinical Research Center, Institute of Medical Science
[5] University of Tokyo,undefined
来源
关键词
AhR; human monocytes and macrophages; transcriptional regulation; endogenous ligand; physiological function;
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学科分类号
摘要
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 α-naphthoflavone inhibits this activation process with reducing CYP1A1 mRNA expression levels, the presence of endogenous ligand is indicated.
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页码:107 / 117
页数:10
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