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dc.contributor.authorGalvão, Viviane-
dc.contributor.authorMiranda, José Garcia Vivas-
dc.creatorGalvão, Viviane-
dc.creatorMiranda, José Garcia Vivas-
dc.date.accessioned2013-10-15T15:23:16Z-
dc.date.issued2009-
dc.identifier.issn0378-4371-
dc.identifier.urihttp://www.repositorio.ufba.br/ri/handle/ri/13242-
dc.descriptionA recent model for Chagas’ disease after stem cell transplantation is extended for a three-dimensional multi-agent-based model. The computational model includes six different types of autonomous agents: inflammatory cell, fibrosis, cardiomyocyte, proinflammatory cytokine tumor necrosis factor-α, Trypanosoma cruzi, and bone marrow stem cell. Only fibrosis is fixed and the other types of agents can move randomly through the empty spaces using the three-dimensional Moore neighborhood. Bone marrow stem cells can promote apoptosis in inflammatory cells, fibrosis regression and can differentiate in cardiomyocyte. T. cruzi can increase the number of inflammatory cells. Inflammatory cells and tumor necrosis factor-α can increase the quantity of fibrosis. Our results were compared with experimental data giving a fairly fit and they suggest that the inflammatory cells are important for the development of fibrosis.pt_BR
dc.description.abstractA recent model for Chagas’ disease after stem cell transplantation is extended for a three-dimensional multi-agent-based model. The computational model includes six different types of autonomous agents: inflammatory cell, fibrosis, cardiomyocyte, proinflammatory cytokine tumor necrosis factor-α, Trypanosoma cruzi, and bone marrow stem cell. Only fibrosis is fixed and the other types of agents can move randomly through the empty spaces using the three-dimensional Moore neighborhood. Bone marrow stem cells can promote apoptosis in inflammatory cells, fibrosis regression and can differentiate in cardiomyocyte. T. cruzi can increase the number of inflammatory cells. Inflammatory cells and tumor necrosis factor-α can increase the quantity of fibrosis. Our results were compared with experimental data giving a fairly fit and they suggest that the inflammatory cells are important for the development of fibrosis.pt_BR
dc.language.isoenpt_BR
dc.sourcehttp://dx.doi.org/10.1016/j.physa.2009.01.012pt_BR
dc.subjectComputational modelpt_BR
dc.subjectChronic chagasic cardiomyopathypt_BR
dc.subjectAutonomous agentpt_BR
dc.subjectCellular therapypt_BR
dc.titleModeling the Chagas’ disease after stem cell transplantationpt_BR
dc.title.alternativePhysica A: Statistical Mechanics and its Applicationspt_BR
dc.typeArtigo de Periódicopt_BR
dc.identifier.numberv. 388, n. 8pt_BR
dc.embargo.liftdate10000-01-01-
Aparece nas coleções:Artigo Publicado em Periódico (FIS)

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