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Type: Journal article
Title: TBK1 and IKKε act redundantly to mediate STING-induced NF-κB responses in myeloid cells
Other Titles: TBK1 and IKKepsilon act redundantly to mediate STING-induced NF-kappaB responses in myeloid cells
Author: Balka, K.R.
Louis, C.
Saunders, T.L.
Smith, A.M.
Calleja, D.J.
D'Silva, D.B.
Moghaddas, F.
Tailler, M.
Lawlor, K.E.
Zhan, Y.
Burns, C.J.
Wicks, I.P.
Miner, J.J.
Kile, B.T.
Masters, S.L.
De Nardo, D.
Citation: Cell Reports, 2020; 31(1):107492-1-107492-22
Publisher: Elsevier
Issue Date: 2020
ISSN: 2211-1247
Statement of
Katherine R. Balka, Cynthia Louis, Tahnee L. Saunders, Amber M. Smith, Dale J. Calleja, Damian B. D’Silva, Fiona Moghaddas, Maximilien Tailler, Kate E. Lawlor, Yifan Zhan, Christopher J. Burns, Ian P. Wicks, Jonathan J. Miner, Benjamin T. Kile, Seth L. Masters, and Dominic De Nardo
Abstract: Stimulator of Interferon Genes (STING) is a critical component of host innate immune defense but can contribute to chronic autoimmune or autoinflammatory disease. Once activated, the cyclic guanosine monophosphate (GMP)-adenosine monophosphate (AMP) (cGAMP) synthase (cGAS)-STING pathway induces both type I interferon (IFN) expression and nuclear factor-κB (NF-κB)-mediated cytokine production. Currently, these two signaling arms are thought to be mediated by a single upstream kinase, TANK-binding kinase 1 (TBK1). Here, using genetic and pharmacological approaches, we show that TBK1 alone is dispensable for STING-induced NF-κB responses in human and mouse immune cells, as well as in vivo. We further demonstrate that TBK1 acts redundantly with IκB kinase ε (IKKε) to drive NF-κB upon STING activation. Interestingly, we show that activation of IFN regulatory factor 3 (IRF3) is highly dependent on TBK1 kinase activity, whereas NF-κB is significantly less sensitive to TBK1/IKKε kinase inhibition. Our work redefines signaling events downstream of cGAS-STING. Our findings further suggest that cGAS-STING will need to be targeted directly to effectively ameliorate the inflammation underpinning disorders associated with STING hyperactivity.
Keywords: Myeloid cells
Rights: © 2020 The Author(s). This is an open access article under the CC BY license (
RMID: 1000018697
DOI: 10.1016/j.celrep.2020.03.056
Grant ID:
Appears in Collections:Medicine publications

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