Cardiac gene expression and systemic cytokine profile are complementary in a murine model of post-ischemic heart failure

dc.creatorLachtermacher, S.
dc.creatorEsporcatte, B. L. B.
dc.creatorMontalvão, F.
dc.creatorCosta, P. C.
dc.creatorRodrigues, D. C.
dc.creatorBelem, L.
dc.creatorRabischoffisky, A.
dc.creatorFaria Neto, Hugo C. C.
dc.creatorVasconcellos, R.
dc.creatorIacobas, S.
dc.creatorDohmann, H. F. R.
dc.creatorSpray, D. C.
dc.creatorGoldenberg, R. C. S.
dc.creatorCarvalho, A. C. Campos de
dc.date2018-12-09T18:10:01Z
dc.date2018-12-09T18:10:01Z
dc.date2010
dc.date.accessioned2023-09-26T21:34:04Z
dc.date.available2023-09-26T21:34:04Z
dc.identifierLACHTERMACHER, S. et al. Cardiac gene expression and systemic cytokine profile are complementary in a murine model of post-ischemic heart failure. Brazilian Journal of Medical and Biological Research, v.43, p.377-389, 2010.
dc.identifier0100-879X
dc.identifierhttps://www.arca.fiocruz.br/handle/icict/30450
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/8872842
dc.descriptionAfter myocardial infarction (MI), activation of the immune system and inflammatory mechanisms, among others, can lead to ventricular remodeling and heart failure (HF). The interaction between these systemic alterations and corresponding changes in the heart has not been extensively examined in the setting of chronic ischemia. The main purpose of this study was to investigate alterations in cardiac gene and systemic cytokine profile in mice with post-ischemic HF. Plasma was tested for IgM and IgG anti-heart reactive repertoire and inflammatory cytokines. Heart samples were assayed for gene expression by analyzing hybridization to AECOM 32k mouse microarrays. Ischemic HF significantly increased the levels of total serum IgM (by 5.2-fold) and total IgG (by 3.6-fold) associated with a relatively high content of anti-heart specificity. A comparable increase was observed in the levels of circulating pro-inflammatory cytokines such as IL-1β (3.8X) and TNF-α (6.0X). IFN-γ was also increased by 3.1-fold in the MI group. However, IL-4 and IL-10 were not significantly different between the MI and sham-operated groups. Chemokines such as MCP-1 and IL-8 were 1.4- and 13-fold increased, respectively, in the plasma of infarcted mice. We identified 2079 well annotated unigenes that were significantly regulated by post-ischemic HF. Complement activation and immune response were among the most up-regulated processes. Interestingly, 21 of the 101 quantified unigenes involved in the inflammatory response were significantly up-regulated and none were down-regulated. These data indicate that post-ischemic heart remodeling is accompanied by immune-mediated mechanisms that act both systemically and locally.
dc.formatapplication/pdf
dc.languageeng
dc.publisherAssociação Brasileira de Divulgação Científica
dc.rightsopen access
dc.subjectInsuficiência cardíaca pós-isquêmica experimental
dc.subjectAnticorpos anti-coração
dc.subjectCitocinas
dc.subjectExperimental post-ischemic heart failure
dc.subjectAnti-heart antibodies
dc.subjectCytokines
dc.subjectImmunoarray
dc.subjectRNAm - Microarray
dc.subjectRNA Mensageiro
dc.titleCardiac gene expression and systemic cytokine profile are complementary in a murine model of post-ischemic heart failure
dc.typeArticle


Este ítem pertenece a la siguiente institución