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Computational analysis reveals the coupling between bistability and the sign of a feedback loop in a TGF-β1 activation model
BACKGROUND: Bistable behaviors are prevalent in cell signaling and can be modeled by ordinary differential equations (ODEs) with kinetic parameters. A bistable switch has recently been found to regulate the activation of transforming growth factor-β1 (TGF-β1) in the context of liver fibrosis, and an...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5763301/ https://www.ncbi.nlm.nih.gov/pubmed/29322934 http://dx.doi.org/10.1186/s12918-017-0508-z |
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author | Li, Huipeng Venkatraman, Lakshmi Narmada, Balakrishnan Chakrapani White, Jacob K. Yu, Hanry Tucker-Kellogg, Lisa |
author_facet | Li, Huipeng Venkatraman, Lakshmi Narmada, Balakrishnan Chakrapani White, Jacob K. Yu, Hanry Tucker-Kellogg, Lisa |
author_sort | Li, Huipeng |
collection | PubMed |
description | BACKGROUND: Bistable behaviors are prevalent in cell signaling and can be modeled by ordinary differential equations (ODEs) with kinetic parameters. A bistable switch has recently been found to regulate the activation of transforming growth factor-β1 (TGF-β1) in the context of liver fibrosis, and an ordinary differential equation (ODE) model was published showing that the net activation of TGF-β1 depends on the balance between two antagonistic sub-pathways. RESULTS: Through modeling the effects of perturbations that affect both sub-pathways, we revealed that bistability is coupled with the signs of feedback loops in the model. We extended the model to include calcium and Krüppel-like factor 2 (KLF2), both regulators of Thrombospondin-1 (TSP1) and Plasmin (PLS). Increased levels of extracellular calcium, which alters the TSP1-PLS balance, would cause high levels of TGF-β1, resembling a fibrotic state. KLF2, which suppresses production of TSP1 and plasminogen activator inhibitor-1 (PAI1), would eradicate bistability and preclude the fibrotic steady-state. Finally, the loop PLS − TGF-β1 − PAI1 had previously been reported as negative feedback, but the model suggested a stronger indirect effect of PLS down-regulating PAI1 to produce positive (double-negative) feedback in a fibrotic state. Further simulations showed that activation of KLF2 was able to restore negative feedback in the PLS − TGF-β1 − PAI1 loop. CONCLUSIONS: Using the TGF-β1 activation model as a case study, we showed that external factors such as calcium or KLF2 can induce or eradicate bistability, accompanied by a switch in the sign of a feedback loop (PLS − TGF-β1 − PAI1) in the model. The coupling between bistability and positive/negative feedback suggests an alternative way of characterizing a dynamical system and its biological implications. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12918-017-0508-z) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5763301 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-57633012018-01-17 Computational analysis reveals the coupling between bistability and the sign of a feedback loop in a TGF-β1 activation model Li, Huipeng Venkatraman, Lakshmi Narmada, Balakrishnan Chakrapani White, Jacob K. Yu, Hanry Tucker-Kellogg, Lisa BMC Syst Biol Research BACKGROUND: Bistable behaviors are prevalent in cell signaling and can be modeled by ordinary differential equations (ODEs) with kinetic parameters. A bistable switch has recently been found to regulate the activation of transforming growth factor-β1 (TGF-β1) in the context of liver fibrosis, and an ordinary differential equation (ODE) model was published showing that the net activation of TGF-β1 depends on the balance between two antagonistic sub-pathways. RESULTS: Through modeling the effects of perturbations that affect both sub-pathways, we revealed that bistability is coupled with the signs of feedback loops in the model. We extended the model to include calcium and Krüppel-like factor 2 (KLF2), both regulators of Thrombospondin-1 (TSP1) and Plasmin (PLS). Increased levels of extracellular calcium, which alters the TSP1-PLS balance, would cause high levels of TGF-β1, resembling a fibrotic state. KLF2, which suppresses production of TSP1 and plasminogen activator inhibitor-1 (PAI1), would eradicate bistability and preclude the fibrotic steady-state. Finally, the loop PLS − TGF-β1 − PAI1 had previously been reported as negative feedback, but the model suggested a stronger indirect effect of PLS down-regulating PAI1 to produce positive (double-negative) feedback in a fibrotic state. Further simulations showed that activation of KLF2 was able to restore negative feedback in the PLS − TGF-β1 − PAI1 loop. CONCLUSIONS: Using the TGF-β1 activation model as a case study, we showed that external factors such as calcium or KLF2 can induce or eradicate bistability, accompanied by a switch in the sign of a feedback loop (PLS − TGF-β1 − PAI1) in the model. The coupling between bistability and positive/negative feedback suggests an alternative way of characterizing a dynamical system and its biological implications. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12918-017-0508-z) contains supplementary material, which is available to authorized users. BioMed Central 2017-12-21 /pmc/articles/PMC5763301/ /pubmed/29322934 http://dx.doi.org/10.1186/s12918-017-0508-z Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Li, Huipeng Venkatraman, Lakshmi Narmada, Balakrishnan Chakrapani White, Jacob K. Yu, Hanry Tucker-Kellogg, Lisa Computational analysis reveals the coupling between bistability and the sign of a feedback loop in a TGF-β1 activation model |
title | Computational analysis reveals the coupling between bistability and the sign of a feedback loop in a TGF-β1 activation model |
title_full | Computational analysis reveals the coupling between bistability and the sign of a feedback loop in a TGF-β1 activation model |
title_fullStr | Computational analysis reveals the coupling between bistability and the sign of a feedback loop in a TGF-β1 activation model |
title_full_unstemmed | Computational analysis reveals the coupling between bistability and the sign of a feedback loop in a TGF-β1 activation model |
title_short | Computational analysis reveals the coupling between bistability and the sign of a feedback loop in a TGF-β1 activation model |
title_sort | computational analysis reveals the coupling between bistability and the sign of a feedback loop in a tgf-β1 activation model |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5763301/ https://www.ncbi.nlm.nih.gov/pubmed/29322934 http://dx.doi.org/10.1186/s12918-017-0508-z |
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