| Literature DB >> 15178328 |
Christina Ehrhardt1, Christian Kardinal, Walter J Wurzer, Thorsten Wolff, Christoph von Eichel-Streiber, Stephan Pleschka, Oliver Planz, Stephan Ludwig.
Abstract
The anti-viral type I interferon (IFN) response is initiated by the immediate induction of IFN beta, which is mainly controlled by the IFN-regulatory factor-3 (IRF-3). The signaling pathways mediating viral IRF-3 activation are only poorly defined. We show that the Rho GTPase Rac1 is activated upon virus infection and controls IRF-3 phosphorylation and activity. Inhibition of Rac1 leads to reduced IFN beta promoter activity and to enhanced virus production. As a downstream mediator of Rac signaling towards IRF-3, we have identified the kinase p21-activated kinase (PAK1). Furthermore, both Rac1 and PAK1 regulate the recently described IRF-3 activators, I kappa B kinase- and TANK-binding kinase-1, establishing a first canonical virus-induced IRF-3 activating pathway.Entities:
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Year: 2004 PMID: 15178328 DOI: 10.1016/j.febslet.2004.04.069
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124