Mechano-chemical Interactions in Cardiac Sarcomere Contraction: A Computational Modeling Study.

We developed a model of cardiac sarcomere contraction to study the calcium-tension relationship in cardiac muscle. Calcium mediates cardiac contraction through its interactions with troponin (Tn) and subsequently tropomyosin molecules. Experimental studies have shown that a slight increase in intrac...

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Main Authors: Lauren J Dupuis, Joost Lumens, Theo Arts, Tammo Delhaas
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2016-10-01
Series:PLoS Computational Biology
Online Access:https://doi.org/10.1371/journal.pcbi.1005126
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spelling doaj-750b21538fd542748e8d2a048fceb6322021-04-21T14:57:10ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582016-10-011210e100512610.1371/journal.pcbi.1005126Mechano-chemical Interactions in Cardiac Sarcomere Contraction: A Computational Modeling Study.Lauren J DupuisJoost LumensTheo ArtsTammo DelhaasWe developed a model of cardiac sarcomere contraction to study the calcium-tension relationship in cardiac muscle. Calcium mediates cardiac contraction through its interactions with troponin (Tn) and subsequently tropomyosin molecules. Experimental studies have shown that a slight increase in intracellular calcium concentration leads to a rapid increase in sarcomeric tension. Though it is widely accepted that the rapid increase is not possible without the concept of cooperativity, the mechanism is debated. We use the hypothesis that there exists a base level of cooperativity intrinsic to the thin filament that is boosted by mechanical tension, i.e. a high level of mechanical tension in the thin filament impedes the unbinding of calcium from Tn. To test these hypotheses, we developed a computational model in which a set of three parameters and inputs of calcium concentration and sarcomere length result in output tension. Tension as simulated appeared in good agreement with experimentally measured tension. Our results support the hypothesis that high tension in the thin filament impedes Tn deactivation by increasing the energy required to detach calcium from the Tn. Given this hypothesis, the model predicted that the areas with highest tension, i.e. closest to the Z-disk end of the single overlap region, show the largest concentration of active Tn's.https://doi.org/10.1371/journal.pcbi.1005126
collection DOAJ
language English
format Article
sources DOAJ
author Lauren J Dupuis
Joost Lumens
Theo Arts
Tammo Delhaas
spellingShingle Lauren J Dupuis
Joost Lumens
Theo Arts
Tammo Delhaas
Mechano-chemical Interactions in Cardiac Sarcomere Contraction: A Computational Modeling Study.
PLoS Computational Biology
author_facet Lauren J Dupuis
Joost Lumens
Theo Arts
Tammo Delhaas
author_sort Lauren J Dupuis
title Mechano-chemical Interactions in Cardiac Sarcomere Contraction: A Computational Modeling Study.
title_short Mechano-chemical Interactions in Cardiac Sarcomere Contraction: A Computational Modeling Study.
title_full Mechano-chemical Interactions in Cardiac Sarcomere Contraction: A Computational Modeling Study.
title_fullStr Mechano-chemical Interactions in Cardiac Sarcomere Contraction: A Computational Modeling Study.
title_full_unstemmed Mechano-chemical Interactions in Cardiac Sarcomere Contraction: A Computational Modeling Study.
title_sort mechano-chemical interactions in cardiac sarcomere contraction: a computational modeling study.
publisher Public Library of Science (PLoS)
series PLoS Computational Biology
issn 1553-734X
1553-7358
publishDate 2016-10-01
description We developed a model of cardiac sarcomere contraction to study the calcium-tension relationship in cardiac muscle. Calcium mediates cardiac contraction through its interactions with troponin (Tn) and subsequently tropomyosin molecules. Experimental studies have shown that a slight increase in intracellular calcium concentration leads to a rapid increase in sarcomeric tension. Though it is widely accepted that the rapid increase is not possible without the concept of cooperativity, the mechanism is debated. We use the hypothesis that there exists a base level of cooperativity intrinsic to the thin filament that is boosted by mechanical tension, i.e. a high level of mechanical tension in the thin filament impedes the unbinding of calcium from Tn. To test these hypotheses, we developed a computational model in which a set of three parameters and inputs of calcium concentration and sarcomere length result in output tension. Tension as simulated appeared in good agreement with experimentally measured tension. Our results support the hypothesis that high tension in the thin filament impedes Tn deactivation by increasing the energy required to detach calcium from the Tn. Given this hypothesis, the model predicted that the areas with highest tension, i.e. closest to the Z-disk end of the single overlap region, show the largest concentration of active Tn's.
url https://doi.org/10.1371/journal.pcbi.1005126
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