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1.
Biol Res ; 48: 45, 2015 Aug 18.
Artículo en Inglés | MEDLINE | ID: mdl-26283227

RESUMEN

BACKGROUND: Low survival rate of transplanted cells compromises the efficacy of cell therapy. Hexokinase II (HKII) is known to have anti-apoptotic activity through its interaction with mitochondria. The objective was to identify miRNAs targeting HKII and investigate whether miRNA-mediated modulation of HKII could improve the survival of mesenchymal stem cells (MSCs) exposed to H2O2. The expression of HKII in MSCs exposed to H2O2 was evaluated, and HKII-targeting miRNA was screened based on miRNA-target prediction databases. The effect of H2O2 on the expression of the selected HKII-targeting miRNA was examined and the effect of modulation of the selected HKII-targeting miRNA using anti-miRNA on H2O2-induced apoptosis of MSC was evaluated. RESULTS: H2O2 (600 µM) induced cell death of MSCs and decreased mitochondrial HKII expression. We have identified miR-181a as a HKII-targeting miRNA and H2O2 increased the expression of miR-181a in MSCs. Delivery of anti-miR-181a, which neutralizes endogenous miR-181a, significantly attenuated H2O2-induced decrease of HKII expression and disruption of mitochondrial membrane potential, improving the survival of MSCs exposed to H2O2. CONCLUSIONS: These findings suggest that H2O2-induced up-regulation of miR-181a contributes to the cell death of MSCs by down-regulating HKII. Neutralizing miR-181a can be an effective way to prime MSCs for transplantation into ischemic tissues.


Asunto(s)
Apoptosis , Glioma/patología , Hexoquinasa/metabolismo , Peróxido de Hidrógeno/toxicidad , Células Madre Mesenquimatosas/patología , MicroARNs/metabolismo , Diferenciación Celular , Movimiento Celular , Supervivencia Celular , Glioma/metabolismo , Humanos , Peróxido de Hidrógeno/administración & dosificación , Glicoproteínas de Membrana/genética , Glicoproteínas de Membrana/metabolismo , Células Madre Mesenquimatosas/efectos de los fármacos , Células Madre Mesenquimatosas/enzimología , MicroARNs/antagonistas & inhibidores , Mitocondrias/enzimología , Invasividad Neoplásica , Especies Reactivas de Oxígeno , Reacción en Cadena en Tiempo Real de la Polimerasa , Semaforinas/genética , Semaforinas/metabolismo
2.
Biol. Res ; 48: 1-7, 2015. graf
Artículo en Inglés | LILACS | ID: biblio-950809

RESUMEN

BACKGROUND: Low survival rate of transplanted cells compromises the efficacy of cell therapy. Hexokinase II (HKII) is known to have anti-apoptotic activity through its interaction with mitochondria. The objective was to identify miRNAs targeting HKII and investigate whether miRNA-mediated modulation of HKII could improve the survival of mesenchymal stem cells (MSCs) exposed to H2O2. The expression of HKII in MSCs exposed to H2O2 was evaluated, and HKII-targeting miRNA was screened based on miRNA-target prediction databases. The effect of H2O2 on the expression of the selected HKII-targeting miRNA was examined and the effect of modulation of the selected HKII-targeting miRNA using anti-miRNA on H2O2-induced apoptosis of MSC was evaluated. RESULTS: H2O2 (600 µM) induced cell death of MSCs and decreased mitochondrial HKII expression. We have identified miR-181a as a HKII-targeting miRNA and H2O2 increased the expression of miR-181a in MSCs. Delivery of anti-miR-181a, which neutralizes endogenous miR-181a, significantly attenuated H2O2-induced decrease of HKII expression and disruption of mitochondrial membrane potential, improving the survival of MSCs exposed to H2O2. CONCLUSIONS: These findings suggest that H2O2-induced up-regulation of miR-181a contributes to the cell death of MSCs by down-regulating HKII. Neutralizing miR-181a can be an effective way to prime MSCs for transplantation into ischemic tissues.


Asunto(s)
Humanos , Apoptosis , MicroARNs/metabolismo , Células Madre Mesenquimatosas/patología , Glioma/patología , Hexoquinasa/metabolismo , Peróxido de Hidrógeno/toxicidad , Glicoproteínas de Membrana/genética , Glicoproteínas de Membrana/metabolismo , Diferenciación Celular , Movimiento Celular , Supervivencia Celular , Especies Reactivas de Oxígeno , Semaforinas/genética , Semaforinas/metabolismo , MicroARNs/antagonistas & inhibidores , Células Madre Mesenquimatosas/efectos de los fármacos , Células Madre Mesenquimatosas/enzimología , Reacción en Cadena en Tiempo Real de la Polimerasa , Glioma/metabolismo , Peróxido de Hidrógeno/administración & dosificación , Mitocondrias/enzimología , Invasividad Neoplásica
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