Rac1 and PAK1 are upstream of IKK-epsilon and TBK-1 in the viral activation of interferon regulatory factor-3 |
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Authors: | Ehrhardt Christina Kardinal Christian Wurzer Walter J Wolff Thorsten von Eichel-Streiber Christoph Pleschka Stephan Planz Oliver Ludwig Stephan |
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Affiliation: | Institute of Molecular Medicine, Heinrich-Heine-Universit?t, Universit?tsstrasse 1, D-40225, Duesseldorf, Germany. christina.bhrhardt@uni-duesseldorf.de |
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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. |
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