Extending the nuclear roles of IκB kinase subunits

被引:41
作者
Gloire, Geoffrey [1 ]
Dejardin, Emmanuel [1 ]
Piette, Jacques [1 ]
机构
[1] CBIG, Virol & Immunol Unit, Inst Pathol B23, B-4000 Liege, Belgium
关键词
NF-kappa B; IKK; inflammation; cytokines; nucleus; DNA damage;
D O I
10.1016/j.bcp.2006.06.017
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The transcription factor NF-kappa B plays a key role in a wide variety of cellular processes such as innate and adaptive immunity, cellular proliferation, apoptosis and development. In unstimulated cells, NF-kappa B is sequestered in the cytoplasm through its tight association with inhibitory proteins called I kappa BS, comprising notably I kappa B alpha. A key step in NF-kappa B activation is the phosphorylation Of I kappa B alpha by the so-called I kappa B kinase (IKK) complex, which targets the inhibitory protein for proteasomal degradation and allows the freed NF-kappa B to enter the nucleus where it can transactivate its target genes. The IKK complex is composed of two catalytic subunits called IKK alpha and IKK beta, and a regulatory subunit called NEMO/IKK gamma. Despite their key role in mediating I kappa B alpha phosphorylation in the cytoplasm, recent works have provided evidence that IKK subunits also translocate into the nucleus to regulate NF-kappa B-dependent and -independent gene expression, paving the way of a novel and exciting field of research. In this review, we will describe the current knowledge in that research area. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:1081 / 1089
页数:9
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