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Title:
Magnetic targeting enhances retrograde cell retention in a rat model of myocardial infarction | Stem Cell Research & Therapy
Description:
Introduction Retrograde coronary venous infusion is a promising delivery method for cellular cardiomyoplasty. Poor cell retention is the major obstacle to the establishment of this method as the preferred route for cell delivery. Here, we explored whether magnetic targeting could enhance retrograde cell retention in a rat model of myocardial infarction. Methods Rat mesenchymal stem cells were labeled with superparamagnetic oxide nanoparticles. The magnetic responsiveness of MSCs was observed while cells flowed through a tube that served as a model of blood vessels in a 0.6-Tesla magnetic field. In a Sprague–Dawley rat model of acute myocardial infarction, 1 × 106 magnetic mesenchymal stem cells were transjugularly injected into the left cardiac vein while a 0.6-Tesla magnet was placed above the heart. The cardiac retention of transplanted cells was assessed by using quantitative Y chromosome-specific polymerase chain reaction, cardiac magnetic resonance imaging, and optical imaging. Cardiac function was measured by using echocardiography, and histologic analyses of infarct morphology and angiogenesis were obtained. Results The flowing iron oxide-labeled mesenchymal stem cells were effectively attracted to the area where the magnet was positioned. Twenty-four hours after cellular retrocoronary delivery, magnetic targeting significantly increased the cardiac retention of transplanted cells by 2.73- to 2.87-fold. Histologic analyses showed that more transplanted cells were distributed in the anterior wall of the left ventricle. The enhanced cell engraftment persisted for at least 3 weeks, at which time, left ventricular remodeling was attenuated, and cardiac function benefit was improved. Conclusions These results suggest that magnetic targeting offers new perspectives for retrograde coronary venous delivery to enhance cell retention and subsequent functional benefit in heart diseases.
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Keywords {🔍}
magnetic, cell, cells, pubmed, article, cardiac, group, left, figure, google, scholar, retrograde, retention, mscs, targeting, heart, delivery, rat, magnet, coronary, vein, stem, wall, model, myocardial, imaging, anterior, magmscs, ventricular, area, infarction, hours, injection, authors, blue, performed, mag, magnetically, hearts, central, cas, analysis, infusion, data, huang, transplanted, weeks, study, density, staining,
Topics {✒️}
iron-labeled cardiosphere-derived cells cardiac-derived stem cells subsequent cell-therapy outcomes prussian blue–positive particles indirect regeneration mechanisms superoxide dismutase-induced cardioprotection consecutive short-axis slices retrograde coronary-delivery strategy intracoronary stem-cell injection permanent neodymium-iron-boron article download pdf cell-treated groups exhibited neodymium-iron-boron spio experimental anterior-wall mi parasternal long-axis view delivery stem cells endothelial progenitor cells dense blue-stained vesicles cardiac regenerative therapy fluorescence-labeled secondary antibodies retrograde cellular therapy magnetic spio-labeled mscs bmc cell biol transjugular cardiac vein therapeutic cell therapy left cardiac vein magnetically loaded cells dmem–lg culture medium optimize targeting parameters nonsurgical catheter-based technique t2 fl2d sequence prussian blue staining left ventricular remodeling retrograde cell retention male-specific sry gene coronary retroinfusion technique full size image spatially targeted therapeutics sprague–dawley rat model unlabeled fourth-passage mscs targeted cell delivery superparamagnetic oxide nanoparticles privacy choices/manage cookies cell dose-effect relation acute cell retention authors’ original file magnetically labeled mscs left vena cava allowing safer access left ventricular function
Questions {❓}
- Chaudeurge A, Wilhelm C, Chen-Tournoux A, Farahmand P, Bellamy V, Autret G, Menager C, Hagege A, Larghero J, Gazeau F, Clement O, Menasche P: Can magnetic targeting of magnetically labeled circulating cells optimize intramyocardial cell retention?
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headline:Magnetic targeting enhances retrograde cell retention in a rat model of myocardial infarction
description:Retrograde coronary venous infusion is a promising delivery method for cellular cardiomyoplasty. Poor cell retention is the major obstacle to the establishment of this method as the preferred route for cell delivery. Here, we explored whether magnetic targeting could enhance retrograde cell retention in a rat model of myocardial infarction. Rat mesenchymal stem cells were labeled with superparamagnetic oxide nanoparticles. The magnetic responsiveness of MSCs was observed while cells flowed through a tube that served as a model of blood vessels in a 0.6-Tesla magnetic field. In a Sprague–Dawley rat model of acute myocardial infarction, 1 × 106 magnetic mesenchymal stem cells were transjugularly injected into the left cardiac vein while a 0.6-Tesla magnet was placed above the heart. The cardiac retention of transplanted cells was assessed by using quantitative Y chromosome-specific polymerase chain reaction, cardiac magnetic resonance imaging, and optical imaging. Cardiac function was measured by using echocardiography, and histologic analyses of infarct morphology and angiogenesis were obtained. The flowing iron oxide-labeled mesenchymal stem cells were effectively attracted to the area where the magnet was positioned. Twenty-four hours after cellular retrocoronary delivery, magnetic targeting significantly increased the cardiac retention of transplanted cells by 2.73- to 2.87-fold. Histologic analyses showed that more transplanted cells were distributed in the anterior wall of the left ventricle. The enhanced cell engraftment persisted for at least 3 weeks, at which time, left ventricular remodeling was attenuated, and cardiac function benefit was improved. These results suggest that magnetic targeting offers new perspectives for retrograde coronary venous delivery to enhance cell retention and subsequent functional benefit in heart diseases.
datePublished:2013-12-12T00:00:00Z
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Cell Retention
Cardiac Vein
Prussian Blue Staining
Magnetic Target
Left Anterior Descend Ligation
Stem Cells
Cell Biology
Regenerative Medicine/Tissue Engineering
Biomedical Engineering and Bioengineering
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headline:Magnetic targeting enhances retrograde cell retention in a rat model of myocardial infarction
description:Retrograde coronary venous infusion is a promising delivery method for cellular cardiomyoplasty. Poor cell retention is the major obstacle to the establishment of this method as the preferred route for cell delivery. Here, we explored whether magnetic targeting could enhance retrograde cell retention in a rat model of myocardial infarction. Rat mesenchymal stem cells were labeled with superparamagnetic oxide nanoparticles. The magnetic responsiveness of MSCs was observed while cells flowed through a tube that served as a model of blood vessels in a 0.6-Tesla magnetic field. In a Sprague–Dawley rat model of acute myocardial infarction, 1 × 106 magnetic mesenchymal stem cells were transjugularly injected into the left cardiac vein while a 0.6-Tesla magnet was placed above the heart. The cardiac retention of transplanted cells was assessed by using quantitative Y chromosome-specific polymerase chain reaction, cardiac magnetic resonance imaging, and optical imaging. Cardiac function was measured by using echocardiography, and histologic analyses of infarct morphology and angiogenesis were obtained. The flowing iron oxide-labeled mesenchymal stem cells were effectively attracted to the area where the magnet was positioned. Twenty-four hours after cellular retrocoronary delivery, magnetic targeting significantly increased the cardiac retention of transplanted cells by 2.73- to 2.87-fold. Histologic analyses showed that more transplanted cells were distributed in the anterior wall of the left ventricle. The enhanced cell engraftment persisted for at least 3 weeks, at which time, left ventricular remodeling was attenuated, and cardiac function benefit was improved. These results suggest that magnetic targeting offers new perspectives for retrograde coronary venous delivery to enhance cell retention and subsequent functional benefit in heart diseases.
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Cardiac Vein
Prussian Blue Staining
Magnetic Target
Left Anterior Descend Ligation
Stem Cells
Cell Biology
Regenerative Medicine/Tissue Engineering
Biomedical Engineering and Bioengineering
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