MRE-binding transcription factor-1 is activated during endotoxemia: a central role for metallothionein

被引:16
|
作者
Kimura, T [1 ]
Itoh, N [1 ]
Takehara, M [1 ]
Oguro, I [1 ]
Ishizaki, J [1 ]
Nakanishi, T [1 ]
Tanaka, K [1 ]
机构
[1] Osaka Univ, Grad Sch Pharmaceut Sci, Dept Toxicol, Suita, Osaka 5650871, Japan
关键词
metallothionein; metal responsive element-binding transcription factor-1; endotoxin; alpha(1)-acid glycoprotein;
D O I
10.1016/S0378-4274(01)00473-8
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Endotoxin (LPS) has been established to induce hepatic rnetallothionein (NIT), but the specific role of MT remains unknown, In this study, we examined whether MT can modulate MTF-1 activity during endotoxemia. Treatment with IL-6. the main mediator of MT induction during endotoxemia, enhanced the expression of the MREd-driven reporter gene. MTF-1 DNA-binding activity was increased 16-24 h after LIPS administration in wild-type mice. white no such activation was observed in MT-null mice during the same period. The expression of alpha(1)-acid gtycoprotein (AGP) mRNA, an RNA regulated by MTF-1, was lower in MT-null than in wild-type mice. Our results suggested that MTF-1 was activated during endotoxemia. MT can act as an activator of MTF-1, and MT can induce MTF-1 targeted gene expression during endotoxemia. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:77 / 84
页数:8
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