The IκB Kinase Complex Is Required for Plexin-B-Mediated Activation of RhoA
Author(s) -
Matthias Zielonka,
Ramesh Kumar Krishnan,
Jakub M. Swiercz,
Stefan Offermanns
Publication year - 2014
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0105661
Subject(s) - rhoa , plexin , iκb kinase , microbiology and biotechnology , kinase , signal transduction , semaphorin , gtpase , small gtpase , biology , transmembrane protein , cancer research , chemistry , nf κb , receptor , genetics
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 IκB 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-κB 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-κB-independent function of the IKK-complex and shows that IKK directs plexin-B signalling to the activation of RhoA.
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