Computational Modeling of Glucose Uptake in the Enterocyte

Absorption of glucose across the epithelial cells of the small intestine is a key process in human nutrition and initiates signaling cascades that regulate metabolic homeostasis. Validated and predictive mathematical models of glucose transport in intestinal epithelial cells are essential for interp...

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Main Authors: Nima Afshar, Soroush Safaei, David P. Nickerson, Peter J. Hunter, Vinod Suresh
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-04-01
Series:Frontiers in Physiology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fphys.2019.00380/full
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spelling doaj-25afdaba26e14097906f5f56bd47c4e72020-11-25T00:28:41ZengFrontiers Media S.A.Frontiers in Physiology1664-042X2019-04-011010.3389/fphys.2019.00380442803Computational Modeling of Glucose Uptake in the EnterocyteNima Afshar0Soroush Safaei1David P. Nickerson2Peter J. Hunter3Vinod Suresh4Vinod Suresh5Auckland Bioengineering Institute, University of Auckland, Auckland, New ZealandAuckland Bioengineering Institute, University of Auckland, Auckland, New ZealandAuckland Bioengineering Institute, University of Auckland, Auckland, New ZealandAuckland Bioengineering Institute, University of Auckland, Auckland, New ZealandAuckland Bioengineering Institute, University of Auckland, Auckland, New ZealandDepartment of Engineering Science, University of Auckland, Auckland, New ZealandAbsorption of glucose across the epithelial cells of the small intestine is a key process in human nutrition and initiates signaling cascades that regulate metabolic homeostasis. Validated and predictive mathematical models of glucose transport in intestinal epithelial cells are essential for interpreting experimental data, generating hypotheses, and understanding the contributions of and interactions between transport pathways. Here we report on the development of such a model that, in contrast to existing models, incorporates mechanistic descriptions of all relevant transport proteins and is implemented in the CellML framework. The model is validated against experimental and simulation data from the literature. It is then used to elucidate the relative contributions of the sodium-glucose cotransporter (SGLT1) and the glucose transporter type 2 (GLUT2) proteins in published measurements of glucose absorption from human intestinal epithelial cell lines. The model predicts that the contribution of SGLT1 dominates at low extracellular glucose concentrations (<20 mM) and short exposure times (<60 s) while the GLUT2 contribution is more significant at high glucose concentrations and long durations. Implementation in CellML permitted a modular structure in which the model was composed by reusing existing models of the individual transporters. The final structure also permits transparent changes of the model components and parameter values in order to facilitate model reuse, extension, and customization (for example, to simplify, or add complexity to specific transporter/pathway models, or reuse the model as a component of a larger framework) and carry out parameter sensitivity studies.https://www.frontiersin.org/article/10.3389/fphys.2019.00380/fullcomputational modelingglucose uptakeSGLT1GLUT2CellMLOpenCOR
collection DOAJ
language English
format Article
sources DOAJ
author Nima Afshar
Soroush Safaei
David P. Nickerson
Peter J. Hunter
Vinod Suresh
Vinod Suresh
spellingShingle Nima Afshar
Soroush Safaei
David P. Nickerson
Peter J. Hunter
Vinod Suresh
Vinod Suresh
Computational Modeling of Glucose Uptake in the Enterocyte
Frontiers in Physiology
computational modeling
glucose uptake
SGLT1
GLUT2
CellML
OpenCOR
author_facet Nima Afshar
Soroush Safaei
David P. Nickerson
Peter J. Hunter
Vinod Suresh
Vinod Suresh
author_sort Nima Afshar
title Computational Modeling of Glucose Uptake in the Enterocyte
title_short Computational Modeling of Glucose Uptake in the Enterocyte
title_full Computational Modeling of Glucose Uptake in the Enterocyte
title_fullStr Computational Modeling of Glucose Uptake in the Enterocyte
title_full_unstemmed Computational Modeling of Glucose Uptake in the Enterocyte
title_sort computational modeling of glucose uptake in the enterocyte
publisher Frontiers Media S.A.
series Frontiers in Physiology
issn 1664-042X
publishDate 2019-04-01
description Absorption of glucose across the epithelial cells of the small intestine is a key process in human nutrition and initiates signaling cascades that regulate metabolic homeostasis. Validated and predictive mathematical models of glucose transport in intestinal epithelial cells are essential for interpreting experimental data, generating hypotheses, and understanding the contributions of and interactions between transport pathways. Here we report on the development of such a model that, in contrast to existing models, incorporates mechanistic descriptions of all relevant transport proteins and is implemented in the CellML framework. The model is validated against experimental and simulation data from the literature. It is then used to elucidate the relative contributions of the sodium-glucose cotransporter (SGLT1) and the glucose transporter type 2 (GLUT2) proteins in published measurements of glucose absorption from human intestinal epithelial cell lines. The model predicts that the contribution of SGLT1 dominates at low extracellular glucose concentrations (<20 mM) and short exposure times (<60 s) while the GLUT2 contribution is more significant at high glucose concentrations and long durations. Implementation in CellML permitted a modular structure in which the model was composed by reusing existing models of the individual transporters. The final structure also permits transparent changes of the model components and parameter values in order to facilitate model reuse, extension, and customization (for example, to simplify, or add complexity to specific transporter/pathway models, or reuse the model as a component of a larger framework) and carry out parameter sensitivity studies.
topic computational modeling
glucose uptake
SGLT1
GLUT2
CellML
OpenCOR
url https://www.frontiersin.org/article/10.3389/fphys.2019.00380/full
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