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脂多糖诱导THP - 1细胞中组织因子的过程涉及Jun蛋白磷酸化和核因子κB的核转位。

Lipopolysaccharide induction of tissue factor in THP-1 cells involves Jun protein phosphorylation and nuclear factor kappaB nuclear translocation.

作者信息

Hall A J, Vos H L, Bertina R M

机构信息

Haemostasis and Thrombosis Research Centre, University Hospital Leiden, Leiden, 2300 RC The Netherlands.

出版信息

J Biol Chem. 1999 Jan 1;274(1):376-83. doi: 10.1074/jbc.274.1.376.

Abstract

Tissue Factor (TF) gene expression is transiently induced in human monocytic THP-1 cells by lipopolysaccharide (LPS). We characterized the transcription factor complexes binding to the TF gene promoter LPS response element (LRE) (-220 to -172), which contains binding sites for nuclear factor kappaB (NFkappaB) and activator protein 1 (AP1) transcription factors, and examined the nature of the activation of these factors during a 24-h time course of LPS stimulation. We found proteolysis of the cytoplasmic inhibitory protein IkappaBalpha and nuclear translocation of the NFkappaB/Rel family proteins p65 and c-Rel, corresponding to the transient binding of a p65/c-Rel heterodimer to the kappaB-like site of the LRE. AP1 binding to the LRE was found to be constitutive, with the majority of the AP1 complexes being JunD/Fra-2 heterodimers. A change in the activation state of the AP1 complexes was, however, found to be transient, as determined by JunD phosphorylation of AP1 bound to the proximal binding site. This directly correlates to the transient activation of Jun N-terminal kinase (SAPK/JNK). These data indicate that LPS induction of TF gene expression in monocytic THP-1 cells is regulated by both the transient phosphorylation of Jun-family proteins and the nuclear translocation and transient binding of NFkappaB/Rel proteins.

摘要

脂多糖(LPS)可短暂诱导人单核细胞THP-1细胞中组织因子(TF)基因的表达。我们对与TF基因启动子LPS反应元件(LRE)(-220至-172)结合的转录因子复合物进行了表征,该元件包含核因子κB(NFκB)和激活蛋白1(AP1)转录因子的结合位点,并在LPS刺激的24小时时间进程中研究了这些因子激活的性质。我们发现细胞质抑制蛋白IκBα发生蛋白水解,NFκB/Rel家族蛋白p65和c-Rel发生核转位,这与p65/c-Rel异二聚体与LRE的κB样位点的短暂结合相对应。发现AP1与LRE的结合是组成性的,大多数AP1复合物是JunD/Fra-2异二聚体。然而,通过与近端结合位点结合的AP1的JunD磷酸化确定,AP1复合物激活状态的变化是短暂的。这与Jun氨基末端激酶(SAPK/JNK)的短暂激活直接相关。这些数据表明,单核细胞THP-1细胞中TF基因表达的LPS诱导受Jun家族蛋白的短暂磷酸化以及NFκB/Rel蛋白核转位和短暂结合的调控。

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