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IKK-i,一种与IκB激酶相关的新型脂多糖诱导激酶。

IKK-i, a novel lipopolysaccharide-inducible kinase that is related to IkappaB kinases.

作者信息

Shimada T, Kawai T, Takeda K, Matsumoto M, Inoue J, Tatsumi Y, Kanamaru A, Akira S

机构信息

Department of Biochemistry, Hyogo College of Medicine, 1-1 Mukogawa-cho, Nishinomiya, Hyogo 663-8501, Japan.

出版信息

Int Immunol. 1999 Aug;11(8):1357-62. doi: 10.1093/intimm/11.8.1357.

Abstract

Using the suppression subtractive hybridization technique, we isolated a novel kinase, IKK-i, whose message is drastically induced by lipopolysaccharide (LPS) in the mouse macrophage cell line RAW264. 7. The predicted protein contains the kinase domain in its N-terminus, which shares 30% identity to that of IKK-alpha or IKK-beta. The C-terminal portion contains a leucine zipper and a potential helix-loop-helix domain, as in the case of IKK-alpha and IKK-beta. IKK-i is expressed mainly in immune cells, and is induced in response to proinflammatory cytokines such as tumor necrosis factor-alpha, IL-1 and IL-6, in addition to LPS. Overexpression of wild-type IKK-i phosphorylated serine residues Ser32 and Ser36 of IkappaB-alpha (preferentially Ser36), and significantly stimulated NF-kappaB activation. These results suggest that IKK-i is an inducible IkappaB kinase which may play a special role in the immune response.

摘要

利用抑制性消减杂交技术,我们分离出一种新型激酶IKK-i,在小鼠巨噬细胞系RAW264.7中,其信使核糖核酸(mRNA)受到脂多糖(LPS)的强烈诱导。预测的蛋白质在其N端含有激酶结构域,与IKK-α或IKK-β的激酶结构域有30%的同源性。与IKK-α和IKK-β一样,C端部分包含一个亮氨酸拉链和一个潜在的螺旋-环-螺旋结构域。IKK-i主要在免疫细胞中表达,除LPS外,对促炎细胞因子如肿瘤坏死因子-α、白细胞介素-1和白细胞介素-6也有反应。野生型IKK-i的过表达使IkappaB-α的丝氨酸残基Ser32和Ser36磷酸化(优先磷酸化Ser36),并显著刺激核因子-κB(NF-κB)的激活。这些结果表明IKK-i是一种可诱导的IkappaB激酶,可能在免疫反应中发挥特殊作用。

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