IκB Kinase Is an Essential Component of the Tpl2 Signaling Pathway

Author:

Waterfield Michael1,Jin Wei1,Reiley William1,Zhang Minying1,Sun Shao-Cong1

Affiliation:

1. Department of Microbiology and Immunology, Pennsylvania State University College of Medicine, Hershey, Pennsylvania 17033

Abstract

ABSTRACT IκB kinase (IKK), a key regulator of immune and inflammatory responses, is known as an effector kinase mediating activation of the transcription factor NF-κB. Whether IKK also participates in other signaling events is not known. Here we show that IKK serves as an essential component of a signaling pathway that involves activation of the Tpl2 kinase and its downstream targets, MEK1 and ERK. Inhibition of IKKβ in macrophages eliminates Tpl2 activation and ERK phosphorylation induced by lipopolysaccharide and tumor necrosis factor alpha. Using IKK-deficient murine fibroblasts, we further demonstrate that IKKβ, but not IKKα, is required for Tpl2 activation. Moreover, this novel function of IKKβ appears to involve phosphorylation and degradation of the Tpl2 inhibitor NF-κB1/p105. These findings suggest that IKKβ exerts its immune-regulatory functions by targeting different downstream signaling pathways.

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

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