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Boolean network modeling of β-cell apoptosis and insulin resistance in type 2 diabetes mellitus

BACKGROUND: Major alteration in lifestyle of human population has promoted Type 2 diabetes mellitus (T2DM) to the level of an epidemic. This metabolic disorder is characterized by insulin resistance and pancreatic β-cell dysfunction and apoptosis, triggered by endoplasmic reticulum (ER) stress, oxid...

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Autores principales: Dutta, Pritha, Ma, Lichun, Ali, Yusuf, Sloot, Peter M.A., Zheng, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6449890/
https://www.ncbi.nlm.nih.gov/pubmed/30953496
http://dx.doi.org/10.1186/s12918-019-0692-0
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author Dutta, Pritha
Ma, Lichun
Ali, Yusuf
Sloot, Peter M.A.
Zheng, Jie
author_facet Dutta, Pritha
Ma, Lichun
Ali, Yusuf
Sloot, Peter M.A.
Zheng, Jie
author_sort Dutta, Pritha
collection PubMed
description BACKGROUND: Major alteration in lifestyle of human population has promoted Type 2 diabetes mellitus (T2DM) to the level of an epidemic. This metabolic disorder is characterized by insulin resistance and pancreatic β-cell dysfunction and apoptosis, triggered by endoplasmic reticulum (ER) stress, oxidative stress and cytokines. Computational modeling is necessary to consolidate information from various sources in order to obtain a comprehensive understanding of the pathogenesis of T2DM and to investigate possible interventions by performing in silico simulations. RESULTS: In this paper, we propose a Boolean network model integrating the insulin resistance pathway with pancreatic β-cell apoptosis pathway which are responsible for T2DM. The model has five input signals, i.e. ER stress, oxidative stress, tumor necrosis factor α (TNF α), Fas ligand (FasL), and interleukin-6 (IL-6). We performed dynamical simulations using random order asynchronous update and with different combinations of the input signals. From the results, we observed that the proposed model made predictions that closely resemble the expression levels of genes in T2DM as reported in the literature. CONCLUSION: The proposed model can make predictions about expression levels of genes in T2DM that are in concordance with literature. Although experimental validation of the model is beyond the scope of this study, the model can be useful for understanding the aetiology of T2DM and discovery of therapeutic intervention for this prevalent complex disease. The files of our model and results are available at https://github.com/JieZheng-ShanghaiTech/boolean-t2dm.
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spelling pubmed-64498902019-04-15 Boolean network modeling of β-cell apoptosis and insulin resistance in type 2 diabetes mellitus Dutta, Pritha Ma, Lichun Ali, Yusuf Sloot, Peter M.A. Zheng, Jie BMC Syst Biol Research BACKGROUND: Major alteration in lifestyle of human population has promoted Type 2 diabetes mellitus (T2DM) to the level of an epidemic. This metabolic disorder is characterized by insulin resistance and pancreatic β-cell dysfunction and apoptosis, triggered by endoplasmic reticulum (ER) stress, oxidative stress and cytokines. Computational modeling is necessary to consolidate information from various sources in order to obtain a comprehensive understanding of the pathogenesis of T2DM and to investigate possible interventions by performing in silico simulations. RESULTS: In this paper, we propose a Boolean network model integrating the insulin resistance pathway with pancreatic β-cell apoptosis pathway which are responsible for T2DM. The model has five input signals, i.e. ER stress, oxidative stress, tumor necrosis factor α (TNF α), Fas ligand (FasL), and interleukin-6 (IL-6). We performed dynamical simulations using random order asynchronous update and with different combinations of the input signals. From the results, we observed that the proposed model made predictions that closely resemble the expression levels of genes in T2DM as reported in the literature. CONCLUSION: The proposed model can make predictions about expression levels of genes in T2DM that are in concordance with literature. Although experimental validation of the model is beyond the scope of this study, the model can be useful for understanding the aetiology of T2DM and discovery of therapeutic intervention for this prevalent complex disease. The files of our model and results are available at https://github.com/JieZheng-ShanghaiTech/boolean-t2dm. BioMed Central 2019-04-05 /pmc/articles/PMC6449890/ /pubmed/30953496 http://dx.doi.org/10.1186/s12918-019-0692-0 Text en © The Author(s) 2019 Open Access This 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
Dutta, Pritha
Ma, Lichun
Ali, Yusuf
Sloot, Peter M.A.
Zheng, Jie
Boolean network modeling of β-cell apoptosis and insulin resistance in type 2 diabetes mellitus
title Boolean network modeling of β-cell apoptosis and insulin resistance in type 2 diabetes mellitus
title_full Boolean network modeling of β-cell apoptosis and insulin resistance in type 2 diabetes mellitus
title_fullStr Boolean network modeling of β-cell apoptosis and insulin resistance in type 2 diabetes mellitus
title_full_unstemmed Boolean network modeling of β-cell apoptosis and insulin resistance in type 2 diabetes mellitus
title_short Boolean network modeling of β-cell apoptosis and insulin resistance in type 2 diabetes mellitus
title_sort boolean network modeling of β-cell apoptosis and insulin resistance in type 2 diabetes mellitus
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6449890/
https://www.ncbi.nlm.nih.gov/pubmed/30953496
http://dx.doi.org/10.1186/s12918-019-0692-0
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