Indirubin and indigo are potent aryl hydrocarbon receptor ligands present in human urine

被引:326
|
作者
Adachi, J
Mori, Y
Matsui, S
Takigami, H
Fujino, J
Kitagawa, H
Miller, CA
Kato, T
Saeki, K
Matsuda, T
机构
[1] Kyoto Univ, Res Ctr Environm Qual Control, Otsu, Shiga 5200811, Japan
[2] Kyoto Univ, Dept Environm Engn, Sakyo Ku, Yoshida Honmachi, Kyoto 6068501, Japan
[3] Tulane Univ, Sch Publ Hlth & Trop Med, Dept Environm Hlth Sci, New Orleans, LA 70112 USA
[4] Tulane Univ, Sch Publ Hlth & Trop Med, Tulane Xavier Ctr Bioenvironm Res, New Orleans, LA 70112 USA
[5] Nagoya City Univ, Fac Pharmaceut Sci, Nagoya, Aichi 4678603, Japan
关键词
D O I
10.1074/jbc.C100238200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Aryl hydrocarbon receptor (AhR) is a ligand-activated transcription factor that regulates genes involved in xenobiotic metabolism, cellular proliferation, and differentiation. Numerous xenobiotic and biological compounds are known to interact with AhR, but it remains an orphan receptor, because its physiological ligand is unknown. We identified AhR ligands in human urine using a yeast AhR signaling assay and then characterized their properties. Two ligands, indirubin and indigo, were both present at average concentrations of similar to0.2 ml in the urine of normal donors. Indirubin was also detected in fetal bovine serum and contributed half of the total AhR ligand activity. The activities of indirubin and indigo were comparable with or more potent than that of the archetypal ligand, 2,3,7,8-tetrachlorodibenzo-p-dioxin, in yeast AhR activation assays. We suggest that the endogenous levels and potencies of indirubin and indigo are such that they activate AhR-mediated signaling mechanisms in vivo.
引用
收藏
页码:31475 / 31478
页数:4
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