Autologous Bone Marrow Mononuclear Cells (BMMC)-Associated Anti-Inflammatory Nanoparticles for Cardiac Repair after Myocardial Infarction

To investigate the effect of transplantation of stem cells from the bone marrow mononuclear cells (BMMC) associated with 15d-PGJ2-loaded nanoparticles in a rat model of chronic MI. Chronic myocardial infarction (MI) was induced by the ligation of the left anterior descending artery in 40 male Wistar...

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Published inJournal of functional biomaterials Vol. 13; no. 2; p. 59
Main Authors Uemura, Laercio, Baggio Simeoni, Rossana, Bispo Machado Júnior, Paulo André, Gavazzoni Blume, Gustavo, Kremer Gamba, Luize, Sgarbossa Tonial, Murilo, Baggio Simeoni, Paulo Ricardo, Stadler Tasca Ribeiro, Victoria, Silvestre, Rodrigo, de Carvalho, Katherine Athayde Teixeira, Napimoga, Marcelo Henrique, Cesar Francisco, Júlio, Guarita-Souza, Luiz Cesar
Format Journal Article
LanguageEnglish
Published Switzerland MDPI AG 13.05.2022
MDPI
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Summary:To investigate the effect of transplantation of stem cells from the bone marrow mononuclear cells (BMMC) associated with 15d-PGJ2-loaded nanoparticles in a rat model of chronic MI. Chronic myocardial infarction (MI) was induced by the ligation of the left anterior descending artery in 40 male Wistar rats. After surgery, we transplanted bone marrow associated with 15d-PGJ2-loaded nanoparticle by intramyocardial injection (10 cells/per injection) seven days post-MI. Myocardial infarction was confirmed by echocardiography, and histological analyses of infarct morphology, gap junctions, and angiogenesis were obtained. Our results from immunohistochemical analyses demonstrated the presence of angiogenesis identified in the transplanted region and that there was significant expression of connexin-43 gap junctions, showing a more effective electrical and mechanical integration of the host myocardium. This study suggests that the application of nanoparticle technology in the prevention and treatment of MI is an emerging field and can be a strategy for cardiac repair.
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ISSN:2079-4983
2079-4983
DOI:10.3390/jfb13020059