Dioxin stimulates synthesis and secretion of IgE-dependent histamine-releasing factor

被引:41
|
作者
Oikawa, K
Ohbayashi, T
Mimura, J
Fujii-Kuriyama, Y
Teshima, S
Rokutan, K
Mukai, Y
Kuroda, M
机构
[1] Tokyo Med Univ, Dept Pathol, Shinjuku Ku, Tokyo 1608402, Japan
[2] Japan Sci & Technol Corp, CREST, Kawaguchi, Saitama 3320012, Japan
[3] Tohoku Univ, Grad Sch Sci, Dept Chem, Aoba Ku, Sendai, Miyagi 9808578, Japan
[4] Univ Tokushima, Sch Med, Dept Nutr, Tokushima 7708503, Japan
关键词
IgE-dependent histamine releasing factor (HRF); aryl hydrocarbon receptor (AhR); 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD; dioxin);
D O I
10.1006/bbrc.2001.6302
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
2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD; dioxin) is the most toxic man-made member of the class of environmental pollutants represented by polychlorinated dibenzo-p-dioxins and dibenzofurans. TCDD produces a wide variety of toxic effects. However, the downstream genes targeted by TCDD and their relation to the diversity of dioxin toxicity symptoms are poorly understood. To identify the target genes of TCDD, we used a cDNA representational difference analysis (RDA) to compare the mRNA patterns of mouse embryonic stem (ES) cells that had and had not been exposed to TCDD. Here we show that TCDD stimulated the expression of IgE-dependent histamine-releasing factor (HRF) mRNA via an aryl hydrocarbon receptor (AhR)-dependent pathway. TCDD also induced the synthesis and secretion of HRF. To our knowledge, this is the first example of HRF being a direct transcriptional target of a toxic agent. HRF has previously been shown to induce histamine release in a dose-dependent manner, at least in vitro. Thus, our data suggest that "endocrine-disrupting" agents may have the potential to influence allergic disorders in the human body. (C) 2002 Elsevier Science (USA).
引用
收藏
页码:984 / 987
页数:4
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