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核因子-κB必需调节因子/κB抑制蛋白激酶γ(NEMO/IKKγ)泛素化在肿瘤坏死因子-α激活κB抑制蛋白激酶复合物中的作用。

A role for NF-kappaB essential modifier/IkappaB kinase-gamma (NEMO/IKKgamma) ubiquitination in the activation of the IkappaB kinase complex by tumor necrosis factor-alpha.

作者信息

Tang Eric D, Wang Cun-Yu, Xiong Yue, Guan Kun-Liang

机构信息

Department of Biological Chemistry, University of Michigan Medical School, Ann Arbor, Michigan 48109, USA.

出版信息

J Biol Chem. 2003 Sep 26;278(39):37297-305. doi: 10.1074/jbc.M303389200. Epub 2003 Jul 16.

Abstract

NEMO (NF-kappaB essential modifier)/IKKgamma (IkappaB kinase-gamma) is required for the activation of the IkappaB kinase complex (IKK) by inflammatory stimuli such as tumor necrosis factor (TNF-alpha). Here we show that TNF-alpha stimulates the ubiquitination of NEMO in a manner that does not appear to target it for degradation and that is impaired by mutations in the NEMO zinc finger. Mutations of the zinc finger are found in patients with hypohidrotic ectodermal dysplasia with immunodeficiency (HED-ID) and lead to the impairment of TNF-alpha-stimulated IKK phosphorylation and activation. In addition, the ubiquitination of NEMO is mediated by c-IAP1, an inhibitor of apoptosis protein that is a component of the TNF receptor signaling complex. Thus, the ubiquitination of NEMO mediated by c-IAP1 likely plays an important role in the activation of IKK by TNF-alpha. Also, defective NEMO ubiquitination may be responsible for the impaired cellular NF-kappaB signaling found in patients with HED-ID.

摘要

NEMO(核因子κB必需调节因子)/IKKγ(IκB激酶γ)是肿瘤坏死因子(TNF-α)等炎性刺激激活IκB激酶复合物(IKK)所必需的。我们在此表明,TNF-α以一种似乎并非将其靶向降解的方式刺激NEMO的泛素化,并且NEMO锌指中的突变会损害这种泛素化。在伴有免疫缺陷的少汗性外胚层发育不良(HED-ID)患者中发现了锌指突变,这些突变导致TNF-α刺激的IKK磷酸化和激活受损。此外,NEMO的泛素化由c-IAP1介导,c-IAP1是一种凋亡抑制蛋白,是TNF受体信号复合物的一个组成部分。因此,由c-IAP1介导的NEMO泛素化可能在TNF-α激活IKK中起重要作用。而且,有缺陷的NEMO泛素化可能是HED-ID患者中细胞NF-κB信号传导受损的原因。

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