Involvement of GSK-3β in TWEAK-mediated NF-κB activation

被引:33
作者
De Ketelaere, A
Vermeulen, L
Vialard, J
Van De Weyer, I
Van Wauwe, J
Haegeman, G
Moelans, I
机构
[1] J&JPRD, Enabling Technol, B-2340 Beerse, Belgium
[2] Univ Ghent, LEGEST, B-9000 Ghent, Belgium
[3] J&JPRD, Oncol, B-2340 Beerse, Belgium
[4] J&JPRD, Funct Genom, B-2340 Beerse, Belgium
[5] J&JPRD, Inflammat, B-2340 Beerse, Belgium
关键词
TWEAK; GSK-3; NF-kappa B;
D O I
10.1016/j.febslet.2004.04.041
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Glycogen synthase kinase-3beta (GSK-3beta) is a key component of several signaling pathways. We found that a short variant of 'TNF-like weak inducer of apoptosis' (shortTWEAK) formed a complex with GSK-3beta in a yeast two-hybrid system. We demonstrate that shortTWEAK and GSK-3beta colocalize in the nucleus of human neuroblastoma cells. We also show that TWEAK is internalized in different cell lines and that it translocates to the nucleus. This event causes the degradation of IBalpha, the nuclear translocation of both GSK-3beta and p65, and the induction of NF-B-driven gene expression. We demonstrate that the induction of IL-8 expression by TWEAK can be counteracted by LiCl. Taken together, these data suggest that GSK-3beta plays an important role in the signal transduction pathway between TWEAK and NF-B. (C) 2004 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:60 / 64
页数:5
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