Agent-Based Modeling of Endotoxin-Induced Acute Inflammatory Response in Human Blood Leukocytes
被引:51
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作者:
Dong, Xu
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机构:
Rutgers State Univ, Dept Biomed Engn, Piscataway, NJ 08855 USARutgers State Univ, Dept Biomed Engn, Piscataway, NJ 08855 USA
Dong, Xu
[1
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Foteinou, Panagiota T.
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机构:
Rutgers State Univ, Dept Biomed Engn, Piscataway, NJ 08855 USARutgers State Univ, Dept Biomed Engn, Piscataway, NJ 08855 USA
Foteinou, Panagiota T.
[1
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Calvano, Steven E.
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机构:
Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Surg, New Brunswick, NJ 08903 USARutgers State Univ, Dept Biomed Engn, Piscataway, NJ 08855 USA
Calvano, Steven E.
[2
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Lowry, Stephen F.
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Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Surg, New Brunswick, NJ 08903 USARutgers State Univ, Dept Biomed Engn, Piscataway, NJ 08855 USA
Lowry, Stephen F.
[2
]
Androulakis, Ioannis P.
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Rutgers State Univ, Dept Biomed Engn, Piscataway, NJ 08855 USARutgers State Univ, Dept Biomed Engn, Piscataway, NJ 08855 USA
Androulakis, Ioannis P.
[1
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机构:
[1] Rutgers State Univ, Dept Biomed Engn, Piscataway, NJ 08855 USA
[2] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Surg, New Brunswick, NJ 08903 USA
Background: Inflammation is a highly complex biological response evoked by many stimuli. A persistent challenge in modeling this dynamic process has been the (nonlinear) nature of the response that precludes the single-variable assumption. Systems-based approaches offer a promising possibility for understanding inflammation in its homeostatic context. In order to study the underlying complexity of the acute inflammatory response, an agent-based framework is developed that models the emerging host response as the outcome of orchestrated interactions associated with intricate signaling cascades and intercellular immune system interactions. Methodology/Principal Findings: An agent-based modeling (ABM) framework is proposed to study the nonlinear dynamics of acute human inflammation. The model is implemented using NetLogo software. Interacting agents involve either inflammation-specific molecules or cells essential for the propagation of the inflammatory reaction across the system. Spatial orientation of molecule interactions involved in signaling cascades coupled with the cellular heterogeneity are further taken into account. The proposed in silico model is evaluated through its ability to successfully reproduce a self-limited inflammatory response as well as a series of scenarios indicative of the nonlinear dynamics of the response. Such scenarios involve either a persistent (non) infectious response or innate immune tolerance and potentiation effects followed by perturbations in intracellular signaling molecules and cascades. Conclusions/Significance: The ABM framework developed in this study provides insight on the stochastic interactions of the mediators involved in the propagation of endotoxin signaling at the cellular response level. The simulation results are in accordance with our prior research effort associated with the development of deterministic human inflammation models that include transcriptional dynamics, signaling, and physiological components. The hypothetical scenarios explored in this study would potentially improve our understanding of how manipulating the behavior of the molecular species could manifest into emergent behavior of the overall system.
机构:
Department of Intensive Care Medicine, Radboud university medical centre, Nijmegen
Radboud Center for Infectious Diseases (RCI), Radboud university medical centre, NijmegenDepartment of Intensive Care Medicine, Radboud university medical centre, Nijmegen
Koch R.M.
Diavatopoulos D.A.
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机构:
Section Pediatric Infectious Diseases, Laboratory of Medical Immunology, Radboud Institute for Molecular Life Sciences, Radboud university medical centre, Nijmegen
Radboud Center for Infectious Diseases (RCI), Radboud university medical centre, NijmegenDepartment of Intensive Care Medicine, Radboud university medical centre, Nijmegen
Diavatopoulos D.A.
Ferwerda G.
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机构:
Section Pediatric Infectious Diseases, Laboratory of Medical Immunology, Radboud Institute for Molecular Life Sciences, Radboud university medical centre, Nijmegen
Radboud Center for Infectious Diseases (RCI), Radboud university medical centre, NijmegenDepartment of Intensive Care Medicine, Radboud university medical centre, Nijmegen
Ferwerda G.
Pickkers P.
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机构:
Department of Intensive Care Medicine, Radboud university medical centre, Nijmegen
Radboud Center for Infectious Diseases (RCI), Radboud university medical centre, NijmegenDepartment of Intensive Care Medicine, Radboud university medical centre, Nijmegen
Pickkers P.
de Jonge M.I.
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机构:
Section Pediatric Infectious Diseases, Laboratory of Medical Immunology, Radboud Institute for Molecular Life Sciences, Radboud university medical centre, Nijmegen
Radboud Center for Infectious Diseases (RCI), Radboud university medical centre, NijmegenDepartment of Intensive Care Medicine, Radboud university medical centre, Nijmegen
de Jonge M.I.
Kox M.
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机构:
Department of Intensive Care Medicine, Radboud university medical centre, Nijmegen
Radboud Center for Infectious Diseases (RCI), Radboud university medical centre, NijmegenDepartment of Intensive Care Medicine, Radboud university medical centre, Nijmegen
机构:
DHE IBRAG UERJ, Lab Reparo Tecidual, Rio De Janeiro, BrazilICB CCS UFRJ, Lab Compartilhado, Estresse Oxidat & Canc, BR-21941902 Rio De Janeiro, Brazil
Lima Trajano, Eduardo Tavares
Sternberg, Cinthya
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INCA, Setor Pesquisa Clin, Rio De Janeiro, BrazilICB CCS UFRJ, Lab Compartilhado, Estresse Oxidat & Canc, BR-21941902 Rio De Janeiro, Brazil
Sternberg, Cinthya
Caetano, Mauricio
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INCA, Setor Pesquisa Clin, Rio De Janeiro, BrazilICB CCS UFRJ, Lab Compartilhado, Estresse Oxidat & Canc, BR-21941902 Rio De Janeiro, Brazil
Caetano, Mauricio
Santos Silva, Marco Aurelio
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DHE IBRAG UERJ, Lab Reparo Tecidual, Rio De Janeiro, BrazilICB CCS UFRJ, Lab Compartilhado, Estresse Oxidat & Canc, BR-21941902 Rio De Janeiro, Brazil
Santos Silva, Marco Aurelio
Porto, Luis Cristovao
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DHE IBRAG UERJ, Lab Reparo Tecidual, Rio De Janeiro, BrazilICB CCS UFRJ, Lab Compartilhado, Estresse Oxidat & Canc, BR-21941902 Rio De Janeiro, Brazil
Porto, Luis Cristovao
Santos, Juliana Carvalho
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USF, Unidade Integrada Farmacol & Gastroenterol, Braganca Paulista, SP, BrazilICB CCS UFRJ, Lab Compartilhado, Estresse Oxidat & Canc, BR-21941902 Rio De Janeiro, Brazil
Santos, Juliana Carvalho
Ribeiro, Marcelo Lima
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USF, Unidade Integrada Farmacol & Gastroenterol, Braganca Paulista, SP, BrazilICB CCS UFRJ, Lab Compartilhado, Estresse Oxidat & Canc, BR-21941902 Rio De Janeiro, Brazil
Ribeiro, Marcelo Lima
Magalhaes, Clarissa Bichara
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机构:
IBCCF CCS UFRJ, Lab Fisiol Resp, Rio De Janeiro, BrazilICB CCS UFRJ, Lab Compartilhado, Estresse Oxidat & Canc, BR-21941902 Rio De Janeiro, Brazil
Magalhaes, Clarissa Bichara
Zin, Walter Araujo
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机构:
IBCCF CCS UFRJ, Lab Fisiol Resp, Rio De Janeiro, BrazilICB CCS UFRJ, Lab Compartilhado, Estresse Oxidat & Canc, BR-21941902 Rio De Janeiro, Brazil
Zin, Walter Araujo
Benjamim, Claudia Farias
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机构:
ICB CCS UFRJ, Lab Compartilhado, Estresse Oxidat & Canc, BR-21941902 Rio De Janeiro, BrazilICB CCS UFRJ, Lab Compartilhado, Estresse Oxidat & Canc, BR-21941902 Rio De Janeiro, Brazil
Benjamim, Claudia Farias
Valenca, Samuel Santos
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机构:
ICB CCS UFRJ, Lab Compartilhado, Estresse Oxidat & Canc, BR-21941902 Rio De Janeiro, BrazilICB CCS UFRJ, Lab Compartilhado, Estresse Oxidat & Canc, BR-21941902 Rio De Janeiro, Brazil