biostudies-literatureUnknown5(4)Passipieri JA<h4>Introduction</h4>The objective of this work was to evaluate the efficacy of placenta-derived mesenchymal stem cell (MSC) therapy in a mouse model of myocardial infarction (MI). Since MSCs can be obtained from two different regions of the human term placenta (chorionic plate or villi), cells obtained from both these regions were compared so that the best candidate for cell therapy could be selected.<h4>Methods</h4>For the in vitro studies, chorionic plate MSCs (cp-MSCs) and chorionic villi MSCs (cv-MSCs) were extensively characterized for their genetic stability, clonogenic and differentiation potential, gene expression, and immunophenotype. For the in vivo studies, C57Bl/6 mice were submitted to MI and, after 21 days, received weekly intramyocardial injections of cp-MSCs for 3 weeks. CStem cell research & therapy102https://www.ebi.ac.uk/biostudies/studies/S-EPMC4354978biostudies-literatureImprovement of cardiac function by placenta-derived mesenchymal stem cells does not require permanent engraftment and is independent of the insulin signaling pathway.PMC4354978Balduino APassipieri JAMartins ABKasai-Brunswick THMello DBRodrigues DCRocha NNLopes LMCarvalho ABCampos DBRamos IPGoldenberg RCCampos de Carvalho ACSa RMSilva-Mendes BJBrasil GVChristie BBSuhett GfalseImprovement of cardiac function by placenta-derived mesenchymal stem cells does not require permanent engraftment and is independent of the insulin signaling pathway.<h4>Introduction</h4>The objective of this work was to evaluate the efficacy of placenta-derived mesenchymal stem cell (MSC) therapy in a mouse model of myocardial infarction (MI). Since MSCs can be obtained from two different regions of the human term placenta (chorionic plate or villi), cells obtained from both these regions were compared so that the best candidate for cell therapy could be selected.<h4>Methods</h4>For the in vitro studies, chorionic plate MSCs (cp-MSCs) and chorionic villi MSCs (cv-MSCs) were extensively characterized for their genetic stability, clonogenic and differentiation potential, gene expression, and immunophenotype. For the in vivo studies, C57Bl/6 mice were submitted to MI and, after 21 days, received weekly intramyocardial injections of cp-MSCs for 3 weeks. C2014-01-01T00:00:00Z2014 Aug2026-04-29T01:47:08.964Z2019-03-27T01:47:56ZS-EPMC43549782514563110.1186/scrt490