Nitric oxide represses inhibitory kappaB kinase through S-nitrosylation

N.L. Reynaert, K. Ckless, S.H. Korn, N. Vos, A.S. Guala, E.F.M. Wouters, A. van der Vliet, Y.M.W. Janssen*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review


Nitric oxide represses inhibitory kappaB kinase through S-nitrosylation.

Reynaert NL, Ckless K, Korn SH, Vos N, Guala AS, Wouters EF, van der Vliet A, Janssen-Heininger YM.

Department of Pathology, University of Vermont, Burlington, VT 05405, USA.

Nitric oxide (NO) possesses antiinflammatory effects, which may be exerted via its ability to inhibit the transcription factor, NF-kappaB. A commonly proposed mode of action for inhibition of NF-kappaBbyNO involves interference with NF-kappaB binding to DNA. Because activation of inhibitory kappaB kinase (IKK), the prerequisite enzyme complex necessary to induce NF-kappaB, is subject to redox regulation, we assessed whether IKK could present a more proximal target for NO to inhibit NF-kappaB activation. We demonstrate here that S-nitrosothiols (SNO) caused a dose-dependent inhibition of the enzymatic activity of IKK, in lung epithelial cells and in Jurkat T cells, which was associated with S-nitrosylation of the IKK complex. Using biotin derivatization of SNO, we revealed that IKKbeta, the catalytic subunit required for NF-kappaB activation, was a direct target for S-nitrosylation. A mutant version of IKKbeta containing a Cys-179-to-Ala mutation was refractory to inhibition by SNO or to increases in S-nitrosylation, in contrast to wild-type IKKbeta, demonstrating that Cys-179 is the main target for attack by SNO. Importantly, inhibition of NO synthase activity in Jurkat T cells resulted in activation of IKK, in association with its denitrosylation. Moreover, NO synthase inhibition enhanced the ability of tumor necrosis factor alpha to activate IKK, illustrating the importance of endogenous NO in regulating the extent of NF-kappaB activation by cytokines. Collectively, our findings demonstrate that IKKbeta is an important target for the redox regulation of NF-kappaB by endogenous or exogenous NO, providing an additional mechanism for its antiinflammatory properties
Original languageEnglish
Pages (from-to)8945-8950
JournalProceedings of the National Academy of Sciences of the United States of America
Issue number24
Publication statusPublished - 1 Jan 2004


Dive into the research topics of 'Nitric oxide represses inhibitory kappaB kinase through S-nitrosylation'. Together they form a unique fingerprint.

Cite this