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评估非死亡性肿瘤坏死因子受体激活替代(非经典)核因子κB途径的方法。

Methods to assess the activation of the alternative (noncanonical) NF-κB pathway by non-death TNF receptors.

作者信息

Remouchamps Caroline, Dejardin Emmanuel

机构信息

Laboratory of Molecular Immunology and Signal Transduction, GIGA-Research, University of Liège, Avenue de l'Hôpital, 1, Sart-Tilman CHU, B34, 4000, Liège, Belgium.

出版信息

Methods Mol Biol. 2015;1280:103-19. doi: 10.1007/978-1-4939-2422-6_7.

Abstract

The alternative or noncanonical NF-κB pathway regulates the generation of p52-containing NF-κB dimers (e.g., p52/RelB) through a partial degradation (called processing) of the precursor p100 into p52. This pathway is activated by a subset of non-death TNF receptor members, which ultimately activate two kinases: NIK (NF-κB-Inducing Kinase) and IKKα (Inhibitor of κB Kinase alpha). These kinases create a phosphodegron for the E3 ligase SCF-β-TrCP that covalently binds K48-linked polyubiquitin chain onto p100 prior to its proteasomal processing. The resulting p52-containing complexes translocate into the nucleus to activate target genes involved in secondary lymphoid organ development, B cell survival or in osteoclastogenesis. We describe in this chapter straightforward methods to monitor the activation of the alternative NF-κB pathway. These methods uncover cytosolic and nuclear biochemical modifications of key proteins of the alternative NF-κB pathway required prior to the transcription of NF-κB target genes.

摘要

非经典或替代NF-κB途径通过前体p100部分降解(称为加工)为p52来调节含p52的NF-κB二聚体(如p52/RelB)的生成。该途径由一部分非死亡TNF受体成员激活,这些成员最终激活两种激酶:NIK(NF-κB诱导激酶)和IKKα(κB激酶α抑制剂)。这些激酶为E3连接酶SCF-β-TrCP创建一个磷酸化降解结构域,该连接酶在p100进行蛋白酶体加工之前将K48连接的多聚泛素链共价结合到p100上。产生的含p52的复合物转运到细胞核中,以激活参与次级淋巴器官发育、B细胞存活或破骨细胞生成的靶基因。在本章中,我们描述了监测替代NF-κB途径激活的直接方法。这些方法揭示了在NF-κB靶基因转录之前替代NF-κB途径关键蛋白的胞质和核生化修饰。

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