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Merging concepts - coupling an agent-based model of hematopoietic stem cells with an ODE model of granulopoiesis

BACKGROUND: Hematopoiesis is a complex process involving different cell types and feedback mechanisms mediated by cytokines. This complexity stimulated various models with different scopes and applications. A combination of complementary models promises to provide their mutual confirmation and to ex...

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Autores principales: Krinner, Axel, Roeder, Ingo, Loeffler, Markus, Scholz, Markus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4228322/
https://www.ncbi.nlm.nih.gov/pubmed/24180697
http://dx.doi.org/10.1186/1752-0509-7-117
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author Krinner, Axel
Roeder, Ingo
Loeffler, Markus
Scholz, Markus
author_facet Krinner, Axel
Roeder, Ingo
Loeffler, Markus
Scholz, Markus
author_sort Krinner, Axel
collection PubMed
description BACKGROUND: Hematopoiesis is a complex process involving different cell types and feedback mechanisms mediated by cytokines. This complexity stimulated various models with different scopes and applications. A combination of complementary models promises to provide their mutual confirmation and to explain a broader range of scenarios. Here we propose a combination of an ordinary differential equation (ODE) model of human granulopoiesis and an agent-based model (ABM) of hematopoietic stem cell (HSC) organization. The first describes the dynamics of bone marrow cell stages and circulating cells under various perturbations such as G-CSF treatment or chemotherapy. In contrast to the ODE model describing cell numbers, our ABM focuses on the organization of individual cells in the stem population. RESULTS: We combined the two models by replacing the HSC compartment of the ODE model by a difference equation formulation of the ABM. In this hybrid model, regulatory mechanisms and parameters of the original models were kept unchanged except for a few specific improvements: (i) Effect of chemotherapy was restricted to proliferating HSC and (ii) HSC regulation in the ODE model was replaced by the intrinsic regulation of the ABM. Model simulations of bleeding, chronic irradiation and stem cell transplantation revealed that the dynamics of hybrid and ODE model differ markedly in scenarios with stem cell damage. Despite these differences in response to stem cell damage, both models explain clinical data of leukocyte dynamics under four chemotherapy regimens. CONCLUSIONS: ABM and ODE model proved to be compatible and were combined without altering the structure of both models. The new hybrid model introduces model improvements by considering the proliferative state of stem cells and enabling a cell cycle-dependent effect of chemotherapy. We demonstrated that it is able to explain and predict granulopoietic dynamics for a large variety of scenarios such as irradiation, bone marrow transplantation, chemotherapy and growth factor applications. Therefore, it promises to serve as a valuable tool for studies in a broader range of clinical applications, in particular where stem cell activation and proliferation are involved.
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spelling pubmed-42283222014-11-13 Merging concepts - coupling an agent-based model of hematopoietic stem cells with an ODE model of granulopoiesis Krinner, Axel Roeder, Ingo Loeffler, Markus Scholz, Markus BMC Syst Biol Research Article BACKGROUND: Hematopoiesis is a complex process involving different cell types and feedback mechanisms mediated by cytokines. This complexity stimulated various models with different scopes and applications. A combination of complementary models promises to provide their mutual confirmation and to explain a broader range of scenarios. Here we propose a combination of an ordinary differential equation (ODE) model of human granulopoiesis and an agent-based model (ABM) of hematopoietic stem cell (HSC) organization. The first describes the dynamics of bone marrow cell stages and circulating cells under various perturbations such as G-CSF treatment or chemotherapy. In contrast to the ODE model describing cell numbers, our ABM focuses on the organization of individual cells in the stem population. RESULTS: We combined the two models by replacing the HSC compartment of the ODE model by a difference equation formulation of the ABM. In this hybrid model, regulatory mechanisms and parameters of the original models were kept unchanged except for a few specific improvements: (i) Effect of chemotherapy was restricted to proliferating HSC and (ii) HSC regulation in the ODE model was replaced by the intrinsic regulation of the ABM. Model simulations of bleeding, chronic irradiation and stem cell transplantation revealed that the dynamics of hybrid and ODE model differ markedly in scenarios with stem cell damage. Despite these differences in response to stem cell damage, both models explain clinical data of leukocyte dynamics under four chemotherapy regimens. CONCLUSIONS: ABM and ODE model proved to be compatible and were combined without altering the structure of both models. The new hybrid model introduces model improvements by considering the proliferative state of stem cells and enabling a cell cycle-dependent effect of chemotherapy. We demonstrated that it is able to explain and predict granulopoietic dynamics for a large variety of scenarios such as irradiation, bone marrow transplantation, chemotherapy and growth factor applications. Therefore, it promises to serve as a valuable tool for studies in a broader range of clinical applications, in particular where stem cell activation and proliferation are involved. BioMed Central 2013-11-01 /pmc/articles/PMC4228322/ /pubmed/24180697 http://dx.doi.org/10.1186/1752-0509-7-117 Text en Copyright © 2013 Krinner et al.; licensee BioMed Central Ltd. http://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), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Krinner, Axel
Roeder, Ingo
Loeffler, Markus
Scholz, Markus
Merging concepts - coupling an agent-based model of hematopoietic stem cells with an ODE model of granulopoiesis
title Merging concepts - coupling an agent-based model of hematopoietic stem cells with an ODE model of granulopoiesis
title_full Merging concepts - coupling an agent-based model of hematopoietic stem cells with an ODE model of granulopoiesis
title_fullStr Merging concepts - coupling an agent-based model of hematopoietic stem cells with an ODE model of granulopoiesis
title_full_unstemmed Merging concepts - coupling an agent-based model of hematopoietic stem cells with an ODE model of granulopoiesis
title_short Merging concepts - coupling an agent-based model of hematopoietic stem cells with an ODE model of granulopoiesis
title_sort merging concepts - coupling an agent-based model of hematopoietic stem cells with an ode model of granulopoiesis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4228322/
https://www.ncbi.nlm.nih.gov/pubmed/24180697
http://dx.doi.org/10.1186/1752-0509-7-117
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