IL-1β stimulates a novel, IKKα -dependent, NIK -independent activation of non-canonical NFκB signalling

McIntosh, Kathryn and Khalaf, Yousif H. and Craig, Rachel and West, Christopher and McCulloch, Ashley and Waghmare, Ajay and Lawson, Christopher and Chan, Edmond Y.W. and MacKay, Simon and Paul, Andrew and Plevin, Robin (2023) IL-1β stimulates a novel, IKKα -dependent, NIK -independent activation of non-canonical NFκB signalling. Cellular Signalling, 107. 110684. ISSN 1873-3913 (https://doi.org/10.1016/j.cellsig.2023.110684)

[thumbnail of McIntosh-etal-CS-2023-IL-1beta-stimulates-a-novel-IKKalpha-dependent-NIK-independent-activation]
Preview
 Text. Filename: McIntosh_etal_CS_2023_IL_1beta_stimulates_a_novel_IKKalpha_dependent_NIK_independent_activation.pdf
Final Published Version
License: Creative Commons Attribution 4.0 logo
Download (4MB)| Preview

Abstract

In this study, we examined the activation of non-canonical nuclear factor Kappa B (NFκB) signalling in U2OS cells, a cellular metastatic bone cancer model. Whilst Lymphotoxin α1β2 (LTα1β2) stimulated the expected slow, delayed, sustained activation of serine 866/870 p100 phosphorylation and increased cellular expression of p52 NFκB, we found that canonical agonists, Interleukin-1β and also Tumour necrosis factor-α (TNFα) generated a rapid transient increase in pp100, which was maximal by 15-30 minutes. This rapid phosphorylation was also observed in other cells types, such as DU145 and HCAECs suggesting the phenomenon is universal. IKKα deletion using CRISPR/Cas9 revealed an IKKα-dependent mechanism for serine 866/870 and additionally serine 872 p100 phosphorylation for both IL-1β and LTα1β2. In contrast, knockdown of IKKα using siRNA or pharmacological inhibition of IKKα activity was without effect on p100 phosphorylation. Pre-incubation of cells with the NFκB inducing-kinase (NIK) inhibitor, CW15337, had no effect on IL-1β induced phosphorylation of p100 however, the response to LTα1β2 was virtually abolished. Surprisingly IL-1β also stimulated p52 nuclear translocation as early as 60 minutes, this response and the concomitant p65 translocation was partially reduced by IKKα deletion. Furthermore, p52 nuclear translocation was unaffected by CW15337. In contrast, the response to LTα1β2 was essentially abolished by both IKKα deletion and CW15337. Taken together, these finding reveal novel forms of NFκB non-canonical signalling stimulated by ligands that activate the canonical NFκB pathway strongly such as IL-1β.

CORE (COnnecting REpositories)