共 57 条
Early growth response-1 regulates lipopolysaccharide-induced suppressor of cytokine signaling-1 transcription
被引:34
作者:

Mostecki, J
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机构: Columbia Univ, Dept Med, Div Pulmonary Allergy & Crit Care, Coll Phys & Surg, New York, NY 10032 USA

Showalter, BM
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机构: Columbia Univ, Dept Med, Div Pulmonary Allergy & Crit Care, Coll Phys & Surg, New York, NY 10032 USA

Rothman, PB
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机构: Columbia Univ, Dept Med, Div Pulmonary Allergy & Crit Care, Coll Phys & Surg, New York, NY 10032 USA
机构:
[1] Columbia Univ, Dept Med, Div Pulmonary Allergy & Crit Care, Coll Phys & Surg, New York, NY 10032 USA
[2] Columbia Univ, Dept Microbiol, Coll Phys & Surg, New York, NY 10032 USA
关键词:
D O I:
10.1074/jbc.M408938200
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:
Suppressor of cytokine signaling (SOCS)-1 is a critical regulator of lipopolysaccharide (LPS) tolerance and LPS-induced cytokine production. The mechanisms regulating the transcription of SOCS-1 in response to LPS are not entirely understood. Functional analysis of the SOCS-1 promoter demonstrates that early growth response-1 (Egr-1) is an important transcriptional regulator of SOCS-1. Two Egr-1 binding sites are present within the SOCS-1 promoter as shown by EMSA and supershift analysis. Further, mutation of the Egr-1 binding sites significantly reduces both the basal and LPS-induced transcriptional activity of the promoter. Chromatin immunoprecipitation experiments confirm LPS-induced binding of Egr-1 to the SOCS-1 promoter in vivo. Additionally, Egr-1(-/-) macrophages show reduced levels of LPS-induced SOCS-1 expression in comparison with macrophages derived from Egr-1(+/+) littermate controls. These results demonstrate an important role for Egr-1 in regulating both the basal and LPS-induced activity of the SOCS-1 promoter.
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页码:2596 / 2605
页数:10
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