Cargando…

Oscillation dynamics underlie functional switching of NF-κB for B-cell activation

Transcription factor nuclear factor kappa B (NF-κB) shows cooperative switch-like activation followed by prolonged oscillatory nuclear translocation in response to extracellular stimuli. These dynamics are important for activation of the NF-κB transcriptional machinery, however, NF-κB activity regul...

Descripción completa

Detalles Bibliográficos
Autores principales: Inoue, Kentaro, Shinohara, Hisaaki, Behar, Marcelo, Yumoto, Noriko, Tanaka, Gouhei, Hoffmann, Alexander, Aihara, Kazuyuki, Okada-Hatakeyama, Mariko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5516862/
https://www.ncbi.nlm.nih.gov/pubmed/28725478
http://dx.doi.org/10.1038/npjsba.2016.24
_version_ 1783251235767320576
author Inoue, Kentaro
Shinohara, Hisaaki
Behar, Marcelo
Yumoto, Noriko
Tanaka, Gouhei
Hoffmann, Alexander
Aihara, Kazuyuki
Okada-Hatakeyama, Mariko
author_facet Inoue, Kentaro
Shinohara, Hisaaki
Behar, Marcelo
Yumoto, Noriko
Tanaka, Gouhei
Hoffmann, Alexander
Aihara, Kazuyuki
Okada-Hatakeyama, Mariko
author_sort Inoue, Kentaro
collection PubMed
description Transcription factor nuclear factor kappa B (NF-κB) shows cooperative switch-like activation followed by prolonged oscillatory nuclear translocation in response to extracellular stimuli. These dynamics are important for activation of the NF-κB transcriptional machinery, however, NF-κB activity regulated by coordinated actions of these dynamics has not been elucidated at the system level. Using a variety of B cells with artificially rewired NF-κB signaling networks, we show that oscillations and switch-like activation of NF-κB can be dissected and that, under some conditions, these two behaviors are separated upon antigen receptor activation. Comprehensive quantitative experiments and mathematical analysis showed that the functional role of switch activation in the NF-κB system is to overcome transient IKK (IκB kinase) activity to amplify nuclear translocation of NF-κB, thereby inducing the prolonged NF-κB oscillatory behavior necessary for target gene expression and B-cell activation.
format Online
Article
Text
id pubmed-5516862
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-55168622017-07-19 Oscillation dynamics underlie functional switching of NF-κB for B-cell activation Inoue, Kentaro Shinohara, Hisaaki Behar, Marcelo Yumoto, Noriko Tanaka, Gouhei Hoffmann, Alexander Aihara, Kazuyuki Okada-Hatakeyama, Mariko NPJ Syst Biol Appl Article Transcription factor nuclear factor kappa B (NF-κB) shows cooperative switch-like activation followed by prolonged oscillatory nuclear translocation in response to extracellular stimuli. These dynamics are important for activation of the NF-κB transcriptional machinery, however, NF-κB activity regulated by coordinated actions of these dynamics has not been elucidated at the system level. Using a variety of B cells with artificially rewired NF-κB signaling networks, we show that oscillations and switch-like activation of NF-κB can be dissected and that, under some conditions, these two behaviors are separated upon antigen receptor activation. Comprehensive quantitative experiments and mathematical analysis showed that the functional role of switch activation in the NF-κB system is to overcome transient IKK (IκB kinase) activity to amplify nuclear translocation of NF-κB, thereby inducing the prolonged NF-κB oscillatory behavior necessary for target gene expression and B-cell activation. Nature Publishing Group 2016-10-20 /pmc/articles/PMC5516862/ /pubmed/28725478 http://dx.doi.org/10.1038/npjsba.2016.24 Text en Copyright © 2016 The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Inoue, Kentaro
Shinohara, Hisaaki
Behar, Marcelo
Yumoto, Noriko
Tanaka, Gouhei
Hoffmann, Alexander
Aihara, Kazuyuki
Okada-Hatakeyama, Mariko
Oscillation dynamics underlie functional switching of NF-κB for B-cell activation
title Oscillation dynamics underlie functional switching of NF-κB for B-cell activation
title_full Oscillation dynamics underlie functional switching of NF-κB for B-cell activation
title_fullStr Oscillation dynamics underlie functional switching of NF-κB for B-cell activation
title_full_unstemmed Oscillation dynamics underlie functional switching of NF-κB for B-cell activation
title_short Oscillation dynamics underlie functional switching of NF-κB for B-cell activation
title_sort oscillation dynamics underlie functional switching of nf-κb for b-cell activation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5516862/
https://www.ncbi.nlm.nih.gov/pubmed/28725478
http://dx.doi.org/10.1038/npjsba.2016.24
work_keys_str_mv AT inouekentaro oscillationdynamicsunderliefunctionalswitchingofnfkbforbcellactivation
AT shinoharahisaaki oscillationdynamicsunderliefunctionalswitchingofnfkbforbcellactivation
AT beharmarcelo oscillationdynamicsunderliefunctionalswitchingofnfkbforbcellactivation
AT yumotonoriko oscillationdynamicsunderliefunctionalswitchingofnfkbforbcellactivation
AT tanakagouhei oscillationdynamicsunderliefunctionalswitchingofnfkbforbcellactivation
AT hoffmannalexander oscillationdynamicsunderliefunctionalswitchingofnfkbforbcellactivation
AT aiharakazuyuki oscillationdynamicsunderliefunctionalswitchingofnfkbforbcellactivation
AT okadahatakeyamamariko oscillationdynamicsunderliefunctionalswitchingofnfkbforbcellactivation