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1.
Chinese Medical Journal ; (24): 3472-3478, 2012.
Artículo en Inglés | WPRIM | ID: wpr-316486

RESUMEN

<p><b>BACKGROUND</b>Exposure of cells to sublethal concentrations of hydrogen peroxide (H2O2) can alleviate subsequent oxidative stress-induced apoptosis. We assessed the effects of H2O2 preconditioning on the therapeutic potential of human umbilical cord Wharton's Jelly mesenchymal stem cells (WJ-MSCs) in a murine model of myocardial infarction.</p><p><b>METHODS</b>WJ-MSCs were incubated in the media for 2 hours with or without 200 µmol/L H2O2. Mice underwent left anterior descending coronary artery ligation, and received injection of phosphate buffered saline, 1×10(6) WJ-MSCs, or 1×10(6) H2O2 preconditioned WJ-MSCs 3 hours later via tail vein. Echocardiography was performed 0, 7, 14 and 28 days after surgery, and the mice were euthanized on day 28 for histological analysis. In vitro cytokine concentrations in the WJ-MSC cell supernatant were measured by enzyme-linked immunosorbent assay (ELISA). The effect of WJ-MSC cell supernatant on the migration and proliferation of endothelial cells were observed by transwell migration and 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazoliumbromide (MTT) assays.</p><p><b>RESULTS</b>Echocardiographic measurements revealed a significant improvement in the left ventricular contractility of the WJ-MSCs-H2O2 group compared to the WJ-MSCs group. Histological analysis revealed increased neovascularization and reduced myocardial fibrosis in the WJ-MSCs-H2O2 group compared to the WJ-MSCs group. Pretreatment of WJ-MSCs with H2O2 increased the secretion of interleukin-6 (IL-6) into the cell culture supernatant by approximately 25-fold. The culture supernatant from WJ-MSCs-H2O2 significantly increased the migration and proliferation of endothelial cells; these effects could be blocked using an anti-IL-6 antibody.</p><p><b>CONCLUSIONS</b>This study demonstrates that H2O2 preconditioning significantly enhanced the therapeutic potential of WJ-MSCs, possibly by stimulating the production of IL-6 by WJ-MSCs, which may cause migration and proliferation of endothelial cells and increase neovascularization.</p>


Asunto(s)
Animales , Humanos , Masculino , Ratones , Movimiento Celular , Fisiología , Ecocardiografía , Ensayo de Inmunoadsorción Enzimática , Peróxido de Hidrógeno , Farmacología , Inmunohistoquímica , Interleucina-6 , Metabolismo , Trasplante de Células Madre Mesenquimatosas , Células Madre Mesenquimatosas , Metabolismo , Ratones Endogámicos C57BL , Infarto del Miocardio , Patología , Terapéutica , Especies Reactivas de Oxígeno , Metabolismo , Gelatina de Wharton , Biología Celular
2.
Journal of Experimental Hematology ; (6): 1084-1087, 2010.
Artículo en Chino | WPRIM | ID: wpr-237590

RESUMEN

Mesenchymal stem cells (MSC) are multipotent cells able to differentiate into multiple lineages including cardiomyocytes and vascular endothelial cells under in vitro culture conditions. In vivo studies have shown that MSC can facilitate angiogenesis, and they localize to the site of ischemic injury which block or reverse the pathologic process. All the data suggest that MSC may be a promising strategy in the treatment of ischemic heart diseases. In recent years, more and more reports demonstrated that researchers have made enormous advances in this field. This review focuses on the angiogenesis and therapeutic applications of MSC derived from human bone marrow, including basic biological features of MSC, role of MSC in angiogenesis, preclinical study of MSC therapy in ischemic heart disease and prospect of MSC application in this disease.


Asunto(s)
Humanos , Trasplante de Células Madre Mesenquimatosas , Métodos , Células Madre Mesenquimatosas , Biología Celular , Isquemia Miocárdica , Cirugía General , Neovascularización Fisiológica
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