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Modeling time delay in the NFκB signaling pathway following low dose IL-1 stimulation

Stimulation of human epithelial cells with IL-1 (10 ng/ml) + UVB radiation results in sustained NFκB activation caused by continuous IKKβ phosphorylation. We have recently published a strictly reduced ordinary differential equation model elucidating the involved mechanisms. Here, we compare model ex...

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Detalles Bibliográficos
Autores principales: Witt, Johannes, Barisic, Sandra, Sawodny, Oliver, Ederer, Michael, Kulms, Dagmar, Sauter, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3171178/
https://www.ncbi.nlm.nih.gov/pubmed/21910922
http://dx.doi.org/10.1186/1687-4153-2011-3
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author Witt, Johannes
Barisic, Sandra
Sawodny, Oliver
Ederer, Michael
Kulms, Dagmar
Sauter, Thomas
author_facet Witt, Johannes
Barisic, Sandra
Sawodny, Oliver
Ederer, Michael
Kulms, Dagmar
Sauter, Thomas
author_sort Witt, Johannes
collection PubMed
description Stimulation of human epithelial cells with IL-1 (10 ng/ml) + UVB radiation results in sustained NFκB activation caused by continuous IKKβ phosphorylation. We have recently published a strictly reduced ordinary differential equation model elucidating the involved mechanisms. Here, we compare model extensions for low IL-1 doses (0.5 ng/ml), where delayed IKKβ phosphorylation is observed. The extended model including a positive regulatory element, most likely auto-ubiquitination of TRAF6, reproduces the observed experimental data most convincingly. The extension is shown to be consistent with the original model and contains very sensitive processes which may serve as potential intervention targets.
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spelling pubmed-31711782011-09-13 Modeling time delay in the NFκB signaling pathway following low dose IL-1 stimulation Witt, Johannes Barisic, Sandra Sawodny, Oliver Ederer, Michael Kulms, Dagmar Sauter, Thomas EURASIP J Bioinform Syst Biol Research Stimulation of human epithelial cells with IL-1 (10 ng/ml) + UVB radiation results in sustained NFκB activation caused by continuous IKKβ phosphorylation. We have recently published a strictly reduced ordinary differential equation model elucidating the involved mechanisms. Here, we compare model extensions for low IL-1 doses (0.5 ng/ml), where delayed IKKβ phosphorylation is observed. The extended model including a positive regulatory element, most likely auto-ubiquitination of TRAF6, reproduces the observed experimental data most convincingly. The extension is shown to be consistent with the original model and contains very sensitive processes which may serve as potential intervention targets. Springer 2011-06-17 /pmc/articles/PMC3171178/ /pubmed/21910922 http://dx.doi.org/10.1186/1687-4153-2011-3 Text en Copyright © 2011 Witt et al; licensee Springer. https://creativecommons.org/licenses/by/2.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0 (https://creativecommons.org/licenses/by/2.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Witt, Johannes
Barisic, Sandra
Sawodny, Oliver
Ederer, Michael
Kulms, Dagmar
Sauter, Thomas
Modeling time delay in the NFκB signaling pathway following low dose IL-1 stimulation
title Modeling time delay in the NFκB signaling pathway following low dose IL-1 stimulation
title_full Modeling time delay in the NFκB signaling pathway following low dose IL-1 stimulation
title_fullStr Modeling time delay in the NFκB signaling pathway following low dose IL-1 stimulation
title_full_unstemmed Modeling time delay in the NFκB signaling pathway following low dose IL-1 stimulation
title_short Modeling time delay in the NFκB signaling pathway following low dose IL-1 stimulation
title_sort modeling time delay in the nfκb signaling pathway following low dose il-1 stimulation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3171178/
https://www.ncbi.nlm.nih.gov/pubmed/21910922
http://dx.doi.org/10.1186/1687-4153-2011-3
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