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NF-κB activation by tumour necrosis factor requires the Akt serine–threonine kinase
Abstract
Activation of the nuclear transcription factor NF-kappaB by inflammatory cytokines requires the successive action of NF-kappaB-inducing kinase (NIK) and an IKB-kinase (IKK) complex composed of IKKalpha and IKKbeta. Here we show that the Akt serine-threonine kinase is involved in the activation of NF-kappaB by tumour necrosis factor (TNF). TNF activates phosphatidylinositol-3-OH kinase (PI(3)K) and its downstream target Akt (protein kinase B). Wortmannin (a PI(3)K inhibitor), dominant-negative PI(3)K or kinase-dead Akt inhibits TNF-mediated NF-kappaB activation. Constitutively active Akt induces NF-kappaB activity and this effect is blocked by dominant-negative NIK. Conversely, NIK activates NF-kappaB and this is blocked by kinase-dead Akt. Thus, both Akt and NIK are necessary for TNF activation of NF-kappaB. Akt mediates IKKalpha phosphorylation at threonine 23. Mutation of this amino acid blocks phosphorylation by Akt or TNF and activation of NF-kappaB. These findings indicate that Akt is part of a signalling pathway that is necessary for inducing key immune and inflammatory responses.
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“The AKT activation of NF-κB is due to stimulation of IKKs and is independent of MEKK1 and NIK, providing an alternate pathway allowing growth factors such as platelet-derived growth factor to activate NF-κB (81-83”
From AKT Induces Transcriptional Activity of PU.1 through Phosphorylation-mediated Modifications within Its Transactivation Domain (2001) · cites this paper as [81]
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Metadata
- Authors
- Nidai Ozes, O., Mayo, L. D., Gustin, J. A., Pfeffer, S. R., Pfeffer, L. M., & Donner, D. B.
- Venue
- Nature
- Published
- 1999-09
- Volume
- 401
- Issue
- 6748
- Pages
- 82-85
- ISSN
- 0028-0836
- 1476-4687
- Cited by
- 1,832
- References
- 0
- Language
- en
- Licence
- www.springer.com/tdm (tdm)
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