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The MAPK Scaffold Kinase Suppressor of Ras Is Involved in ERK Activation by Stress and Proinflammatory Cytokines and Induction of Arthritis
Author(s) -
Angela M. Fusello,
Laura MandikNayak,
Fei F. Shih,
Robert E. Lewis,
Paul M. Allen,
Andréy S. Shaw
Publication year - 2006
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.177.9.6152
Subject(s) - mapk/erk pathway , proinflammatory cytokine , microbiology and biotechnology , kinase , in vivo , arthritis , tumor necrosis factor alpha , chemistry , inflammation , cancer research , immunology , medicine , biology
The MAPK ERK is required for LPS-induced TNF production by macrophages. Although the scaffold kinase suppressor of Ras (KSR)1 is required for efficient Erk activation by mitogenic stimuli, the role of KSR1 in ERK activation by inflammatory and stress stimuli is unknown. In this study, we examined the effects of KSR deficiency on ERK activation by stress stimuli and show that ERK activation by TNF, IL-1, and sorbitol is attenuated in the absence of KSR1. To determine the significance of this defect in vivo, we tested KSR-deficient mice using a passive transfer model of arthritis. We found that the induction of arthritis is impaired in the absence of KSR. Thus, KSR plays a role in ERK activation during inflammatory and stress responses both in vitro and in vivo.

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