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J Cell Mol Med ; 22(11): 5759-5763, 2018 11.
Artículo en Inglés | MEDLINE | ID: mdl-30160360

RESUMEN

The aim of this study is to optimize the timing of erythropoietin gene modified mesenchymal stem cells (EPO-MSCs) transplantation for bronchopulmonary dysplasia (BPD). Three weeks post-operation, the results indicated that the damage of airway structure and apoptosis were significantly decreased, the proliferation was increased in three EPO-MSCs transplantation groups as compared with BPD mice. Moreover, the inflammation cytokines were improvement in early EPO-MSCs injection mice than in BPD mice, but there was no significant difference between late injection and BPD groups. Furthermore, the protein expression ratio of p-p38/p38MAPK was down-regulation in early mice but not in late transplantation mice. Our findings suggest that EPO-MSCs maybe attenuate BPD injury in early than in late administration by inhibiting inflammation response through down-regulation of the p38MAPK signalling pathway.


Asunto(s)
Displasia Broncopulmonar/terapia , Eritropoyetina/genética , Trasplante de Células Madre Mesenquimatosas , Proteínas Quinasas p38 Activadas por Mitógenos/genética , Animales , Apoptosis/genética , Displasia Broncopulmonar/genética , Displasia Broncopulmonar/patología , Proliferación Celular/genética , Modelos Animales de Enfermedad , Eritropoyetina/administración & dosificación , Regulación de la Expresión Génica/genética , Humanos , Recién Nacido , Células Madre Mesenquimatosas/efectos de los fármacos , Células Madre Mesenquimatosas/metabolismo , Ratones , Transducción de Señal/genética
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