Aryl hydrocarbon receptor-mediated suppression of GH receptor and Janus kinase 2 expression in mice

被引:23
作者
Nukaya, M
Takahashi, Y
Gonzalez, FJ
Kamataki, T
机构
[1] Hokkaido Univ, Grad Sch Pharmaceut Sci, Div Pharmacobio Dynam, Lab Drug Metab,Kita Ku, Sapporo, Hokkaido 0600812, Japan
[2] NCI, Lab Metab, Bethesda, MD 20892 USA
关键词
aryl hydrocarbon receptor; growth hormone receptor; 3-methylcholanthrene; Janus kinase 2; major urinary protein; signal transducer and activator of transcription 5; wasting syndrome;
D O I
10.1016/S0014-5793(03)01528-X
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
Differential mRNA display revealed that a cDNA encoding the major urinary protein 2 (MUP2) that belongs to the lipocalin superfamily was absent in livers of mice treated with 3-methylcholanthrene (MC). The expression of MUP2 is known to be stimulated by growth hormone (GH), through the GH receptor (GUR), Janus kinase 2 (JAK2) and signal transducer and activator of transcription 5 (STAT5) signal transduction pathway. Since MC is an aryl hydrocarbon receptor (AhR) ligand, the effects of MC treatment on the expression of GHR, JAK2 or STAT5 in the livers of wild-type or AhR-null mice were examined. The result indicated that the expression of GHR and JAK2 mRNA was greatly decreased by MC in wildtype mice but not in AhR-null mice. In addition, the binding activity of STAT5 bound to STAT5-binding element was reduced after MC treatment in wild-type mice but not in AhR-null mice. Based on these results, we conclude that the suppression of MUP2 mRNA expression by MC is caused by the AhR-mediated disruption of the GH signaling pathway. Possible mechanism(s) by which exposure to aromatic hydrocarbons causes a decrease in the body weight of mice, which has been referred to as wasting syndrome, will also be discussed. (C) 2004 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:96 / 100
页数:5
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