The IκB Kinase Complex Is Required for Plexin-B-Mediated Activation of RhoA

被引:2
|
作者
Zielonka, Matthias [1 ,2 ]
Krishnan, Ramesh K. [1 ]
Swiercz, Jakub M. [1 ]
Offermanns, Stefan [1 ,3 ]
机构
[1] Max Planck Inst Heart & Lung Res, Dept Pharmacol, Bad Nauheim, Germany
[2] Heidelberg Univ, Inst Pharmacol, Heidelberg, Germany
[3] Goethe Univ Frankfurt, Fac Med, D-60054 Frankfurt, Germany
来源
PLOS ONE | 2014年 / 9卷 / 08期
关键词
SIGNALING PATHWAYS; SEMAPHORIN; 4D; RECEPTOR PLEXIN-B1; TUMOR ANGIOGENESIS; CANCER METASTASIS; MELANOMA-CELLS; IKK-ALPHA; PROTEINS; GROWTH; TRANSMEMBRANE;
D O I
10.1371/journal.pone.0105661
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Plexins are widely expressed transmembrane proteins that mediate the cellular effects of semaphorins. The molecular mechanisms of plexin-mediated signal transduction are still poorly understood. Here we show that signalling via B-family plexins leading to the activation of the small GTPase RhoA requires activation of the I kappa B kinase (IKK)-complex. In contrast, plexin-B-dependent regulation of R-Ras activity is not affected by IKK activity. This regulation of plexin signalling depends on the kinase activity of the IKK-complex, but is independent of NF-kappa B activation. We confirm that the IKK-complex is active in tumour cells and osteoblasts, and we demonstrate that plexin-B-dependent tumour cell invasiveness and regulation of osteoblast differentiation require an active IKK-complex. This study identifies a novel, NF-kappa B-independent function of the IKK-complex and shows that IKK directs plexin-B signalling to the activation of RhoA.
引用
收藏
页数:13
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