Journal
JOURNAL OF IMMUNOLOGY
Volume 204, Issue 2, Pages 418-427Publisher
AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.1900626
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Funding
- National Natural Science Foundation of China [31730026, 81525012, 81930039, 31570912]
- Natural Science Foundation of Shandong Province [ZR2014CQ006, ZR2017BH084]
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Stringent regulation of the transcription factor NF-kappa B signaling is essential for the activation of host immune responses and maintaining homeostasis, yet the molecular mechanisms involved in its tight regulation are not completely understood. In this study, we report that IKK-interacting protein (IKIP) negatively regulates NF-kappa B activation. IKIP interacted with IKK alpha/beta to block its association with NEMO, thereby inhibiting the phosphorylation of IKK alpha/beta and the activation of NF-kappa B. Upon LPS, TNF-alpha, and IL-1 beta stimulation, IKIP-deficient macrophages exhibited more and prolonged IKK alpha/beta phosphorylation, I kappa B, and p65 phosphorylation and production of NF-kappa B-responsive genes. Moreover, IKIP-deficient mice were more susceptible to LPS-induced septic shock and dextran sodium sulfate-induced colitis. Our study identifies a previously unrecognized role for IKIP in the negative regulation of NF-kappa B activation by inhibition of IKK alpha/beta phosphorylation through the disruption of IKK complex formation.
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